502 results on '"Spina, V."'
Search Results
152. Surgical repair of absence of vagina, with special reference to the agenesis of vagina
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Saivatores, C. A., primary, Lodovici, O., additional, and Spina, V., additional
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- 1965
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153. Use of Dorranceʼs method in reconstruction of extensive defects of the soft palate (Aproveitamento de metodo de Dorrance na reconstitucao de extensa perda de palato mole)
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Spina, V., primary
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- 1954
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154. Treatment of nasal deformities in bilateral harelip
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Spina, V., primary and Zaputovich, V., additional
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- 1968
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155. Breast hypertrophy. Its treatment by the technique of Strömbeck
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Spina, V., primary, Degrazia, L., additional, Kamakura, L., additional, Teixeira, D., additional, and Lodovici, O., additional
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- 1968
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156. Pendulous Abdomen
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Spina, V, primary
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- 1953
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157. Rare Congenital Facial Clefts
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Spina, V, primary and Rutledge, G, additional
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- 1957
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158. Persistent cloaca: are we ready for a correct prenatal diagnosis?
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Zaccara, A, Gatti, C, Silveri, M, Rivosecchi, M, Bilancioni, E, Spina, V, Giorlandino, C, De Gennaro, M, and Bagolan, P
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- 1999
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159. L'IRM dans le contrôle des pseudarthroses du scaphoïde carpien traitées par greffe cortico-spongieuse: A propos de 31 cas étudiés
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Marcuzzi, A., Spina, V., Adani, R., Mustapha, B., and Caroli, A.
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- 1998
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160. Stereotyped B-Cell Receptor Is an Independent Risk Factor of Chronic Lymphocytic Leukemia Transformation to Richter Syndrome
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Francesco Forconi, Michaela Cerri, Emanuele Zucca, Stefano Pileri, Marco Ladetto, Rossana Maffei, Caroline Besson, Silvia Rasi, Antonello Cabras, Valter Gattei, Antonino Carbone, Silvia Deaglio, Roberto Marasca, Maurizio Martini, Joseph F. Nomdedeu, Lorenzo De Paoli, Luigi Maria Larocca, Valeria Spina, Marco Paulli, Davide Rossi, Vincenzo Canzonieri, Luca Laurenti, Marco Lucioni, Francesco Bertoni, Antonio Ramponi, Claudio Agostinelli, Michele Magni, Gianluca Gaidano, Clara Deambrogi, Rossi, D, Spina, V, Cerri, M, Rasi, S, Deambrogi, C, De Paoli, L, Laurenti, L, Maffei, R, Forconi, F, Bertoni, F, Zucca, E, Agostinelli, C, Cabras, A, Lucioni, M, Martini, M, Magni, M, Deaglio, S, Ladetto, M, Nomdedeu, Jf, Besson, C, Ramponi, A, Canzonieri, V, Paulli, M, Marasca, R, Larocca, Lm, Carbone, A, Pileri, Sa, Gattei, V, Gaidano, G, Rossi D, Spina V, Cerri M, Rasi S, Deambrogi C, De Paoli L, Laurenti L, Maffei R, Forconi F, Bertoni F, Zucca E, Agostinelli C, Cabras A, Lucioni M, Martini M, Magni M, Deaglio S, Ladetto M, Nomdedeu JF, Besson C, Ramponi A, Canzonieri V, Paulli M, Marasca R, Larocca LM, Carbone A, Pileri SA, Gattei V, and Gaidano G.
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Oncology ,Male ,Cancer Research ,Lymphoma ,Chronic lymphocytic leukemia ,Aggressive lymphoma ,Cohort Studies ,Gene Frequency ,immune system diseases ,Risk Factors ,hemic and lymphatic diseases ,Chronic ,genetics/physiology ,chronic lymphocytic leukemia ,B cell receptor ,Richter syndrome ,Leukemia ,breakpoint cluster region ,Syndrome ,Middle Aged ,Lymphocytic ,immunoglobulin genes ,Proto-Oncogene Proteins c-bcr ,Disease Progression ,Female ,medicine.medical_specialty ,B-cell receptor ,diffuse large B-cell lymphoma ,Genetic ,Aged, Cohort Studies, Disease Progression, Female, Gene Frequency, Genetic Predisposition to Disease, Humans, Leukemia ,B-Cell ,complications/genetics/pathology, Lymphoma ,genetics/pathology, Male, Middle Aged, Neoplasm Invasiveness, Polymorphism ,physiology, Proto-Oncogene Proteins c-bcr ,genetics/physiology, Risk Factors, Syndrome ,Internal medicine ,medicine ,Humans ,Genetic Predisposition to Disease ,Neoplasm Invasiveness ,Polymorphism ,Risk factor ,Aged ,Polymorphism, Genetic ,Settore MED/08 - ANATOMIA PATOLOGICA ,complications/genetics/pathology ,business.industry ,transformation ,genetics/pathology ,medicine.disease ,Leukemia, Lymphocytic, Chronic, B-Cell ,physiology ,Immunology ,business ,Diffuse large B-cell lymphoma - Abstract
Purpose: Few biological prognosticators are useful for prediction of Richter syndrome (RS), representing the transformation of chronic lymphocytic leukemia (CLL) to aggressive lymphoma. Stereotyped B-cell receptors (BCR) may have prognostic effect in CLL progression. We tested the prognostic effect of stereotyped BCR for predicting RS transformation.Experimental Design: The prevalence of stereotyped BCR was compared in RS (n = 69) versus nontransformed CLL (n = 714) by a case-control analysis. Subsequently, the effect of stereotyped BCR at CLL diagnosis on risk of RS transformation was actuarially assessed in a consecutive CLL series (n = 753).Results: RS (n = 69) displayed a higher prevalence of stereotyped BCR (P < 0.001) compared with nontransformed CLL. The actuarial risk of RS transformation was significantly higher in CLL carrying stereotyped BCR (P < 0.001). Among BCR subsets most represented in CLL, subset 8 using IGHV4-39/IGHD6-13/IGHJ5 carried the highest risk of RS transformation [hazard ratio (HR), 24.50; P < 0.001]. Multivariate analysis selected stereotyped BCR (HR, 3.33; P = 0.001) and IGHV4-39 usage (HR, 4.03; P = 0.004) as independent predictors of RS transformation. The combination of IGHV4-39 usage and stereotyped BCR in the same patient identified CLL with a very high risk of RS transformation (5-year risk, 68.7%). The risk carried by stereotyped BCR and IGHV4-39 usage was specific for RS transformation and had no effect on CLL progression without transformation.Conclusions: Analysis of BCR features may help identify CLL patients at risk of RS. A close monitoring and a careful biopsy policy may help early recognition of RS in CLL patients using stereotyped BCR, particularly if combined with IGHV4-39.
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- 2009
161. Sedimentological and stratigraphic signature of the Plio-Pleistocene tectonic events in the Southern Apennines, Italy: The Calvello-Anzi Basin case study
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Danica Jablonska, Stefano Mazzoli, Valentino Di Donato, Vincenzo Spina, Alan Pitts, Emanuele Tondi, Claudio Di Celma, Pitts, A. D., Jablonska, D., Di Donato, V., Mazzoli, S., Spina, V., Di Celma, C., and Tondi, E.
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Extensional fault ,Piacenzian ,010504 meteorology & atmospheric sciences ,Stratigraphy ,Geology ,Plio-Pleistocene ,Structural basin ,010502 geochemistry & geophysics ,Oceanography ,01 natural sciences ,Unconformity ,Sedimentary depositional environment ,Paleontology ,Geophysics ,Facies ,Economic Geology ,Sedimentary rock ,Calvello BasinPiggy-backPleistocenePlioceneSouthern ApenninesTectonicsThrust-top ,0105 earth and related environmental sciences - Abstract
The Plio-Pleistocene Calvello-Anzi Basin (CAB) represents a synorogenic shallow marine to alluvial succession deposited during the late phase of the Apennine Orogenic event. While the stratigraphy and sedimentary cycles are well known, the precise role and timing of the tectonic phases affecting this area are unclear. In this paper we report the major findings from a study aimed at unraveling the signatures of the Plio-Quaternary tectonic events affecting the CAB and this portion of the Southern Apennines by using a field integrated approach characterized by facies analysis, structural surveying, and basin architecture. The CAB is located in the axial portion of the Southern Apennine chain and has a roughly E-W orientation which is at a high angle with respect the main NW-SE striking regional tectonic structures controlling the foreland-directed migration of the compression. In the study area, an approximately 1,200-meter-thick package of Zanclean (early-middle Pliocene) to Santernian (middle Pleistocene) shelf, shallow marine, and alluvial deposits accumulated during the late stages of the Apennine orogenic evolution. Within the CAB deposits we recognize two main depositional motifs which roughly correspond to previously established regional cycles that are genetically linked to two corresponding tectonic phases of the Southern Apennine chain. Our results reveal how these two main tectonic phases played a primary role in controlling the depositional architecture, facies, depocenter distribution, and the basin shape throughout the CAB's lifespan. In the proposed model, during the first depositional stage (Zanclean), the CAB formed as a wedge-top basin, controlled by the subsurface propagation of NW-SE-trending thrusts related to the main NE-SW directed shortening of the Apennines. This stage is recorded in the basal units of the CAB infill by progressive unconformities, the development of syn-tectonic shallow marine sedimentary wedges along a high gradient tectonically controlled depositional surface, and a marked SE migration of the main depocenter. During the second depositional stage (upper Piacenzian to Santernian), the CAB was controlled by a series of roughly E-W-trending normal faults which crosscut the preexisting compressional structural fabric. Syndepositional activity along these faults played a direct role in creating an E-W oriented tectonic depression and controlling the accommodation space for the upper portion of the CAB infill. This second stage is marked by two points of evidence. The first point is revealed by a southwestward migration of the CAB depocenter driven by ~90-degree rotation from a roughly NW-SE elongated pattern to roughly elongated W-E transverse to the Pliocene regional structural fabric. This depocenter drift also coincides with an abrupt change in depositional regime from shallow marine to continental sedimentation. The second and most important point of evidence is the presence of several basin-bounding extensional fault zones which cut the lower Pliocene basin-fill units. We relate these features to the middle upper Pleistocene transition to along-strike extension, widely reported in the Southern Apennines, which is related to the overall extensional regime that is acting on the chain also at present. Data from this study provide additional insight into the evolution of the Southern Apennine chain, the formation of the Plio-Pleistocene CAB, and the debated role of Quaternary tectonics on the basin's development during the post-collision orogenic phases. Given the proximity of the study area with several oil fields and considering that hydrocarbon traps in Southern Apennines are Plio-Quaternary in age, the constraints provided on the timing and the style of the regional deformation may improve the definitions of hydrocarbon traps in the buried Apulian platform.
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- 2020
162. Biological and clinical implications of BIRC3 mutations in chronic lymphocytic leukemia
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Francesca Romana Mauro, Sruthi Sagiraju, Davide Rossi, Giovanni Del Poeta, Denise Peroni, Silvia Rasi, Ken I. Mills, Gian Matteo Rigolin, Sarah Lawless, Riccardo Bomben, Ilaria Del Giudice, Annalisa Chiarenza, Robin Foà, Francesca Arruga, Fary Diop, Alessio Bruscaggin, Marina Motta, Luca Laurenti, Marta Coscia, Ramesh Adhinaveni, Lorenzo De Paoli, Patrick Thornton, Phil Weir, Chiara Favini, Simone Favini, Riccardo Moia, Roberto Marasca, Carlo Visco, Antonio Cuneo, Omar Perbellini, Antonia Follenzi, Lodovico Terzi-di-Bergamo, Francesca Rossi, Renzo Boldorini, Andrea Patriarca, Alessandra Tedeschi, Clara Deambrogi, Ahad Ahmed Kodipad, Elisa Spaccarotella, Mark Catherwood, Chiara Tarantelli, Clive Jabangwe, Valeria Spina, Francesco Forconi, Francesco Bertoni, Francesco Zaja, David Donaldson, Valter Gattei, Gianluca Gaidano, Agostino Cortelezzi, Silvia Deaglio, Diop, F., Moia, R., Favini, C., Spaccarotella, E., De Paoli, L., Bruscaggin, A., Spina, V., Terzi-Di-Bergamo, L., Arruga, F., Tarantelli, C., Deambrogi, C., Rasi, S., Adhinaveni, R., Patriarca, A., Favini, S., Sagiraju, S., Jabangwe, C., Kodipad, A. A., Peroni, D., Mauro, F. R., Del Giudice, I., Forconi, F., Cortelezzi, A., Zaja, F., Bomben, R., Rossi, F. M., Visco, C., Chiarenza, A., Rigolin, G. M., Marasca, R., Coscia, M., Perbellini, O., Tedeschi, A., Laurenti, L., Motta, M., Donaldson, D., Weir, P., Mills, K., Thornton, P., Lawless, S., Bertoni, F., Poeta, G. D., Cuneo, A., Follenzi, A., Gattei, V., Boldorini, R. L., Catherwood, M., Deaglio, S., Foa, R., Gaidano, G., and Rossi, D.
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Oncology ,medicine.medical_specialty ,Cyclophosphamide ,Chronic lymphocytic leukemia ,chronic lymphocytic leukemia ,BIRC-3 ,prognosis ,medicine.disease_cause ,Chronic Lymphocytic Leukemia ,Cytogenetics and Molecular Genetics ,Molecular predictors ,Article ,NO ,03 medical and health sciences ,0302 clinical medicine ,Chemoimmunotherapy ,Internal medicine ,medicine ,Univariate analysis ,Mutation ,BIRC3 CLL prognosis ,business.industry ,Hematology ,medicine.disease ,Settore MED/15 ,3. Good health ,Fludarabine ,Leukemia ,Settore MED/15 - MALATTIE DEL SANGUE ,Birc3 ,IGHV@ ,business ,030215 immunology ,medicine.drug - Abstract
BIRC3 is a recurrently mutated gene in chronic lymphocytic leukemia (CLL) but the functional implications of BIRC3 mutations are largely unexplored. Furthermore, little is known about the prognostic impact of BIRC3 mutations in CLL cohorts homogeneously treated with first-line fludarabine, cyclophosphamide, and rituximab (FCR). By immunoblotting analysis, we showed that the non-canonical nuclear factor-κB pathway is active in BIRC3-mutated cell lines and in primary CLL samples, as documented by the stabilization of MAP3K14 and by the nuclear localization of p52. In addition, BIRC3-mutated primary CLL cells are less sensitive to flu-darabine. In order to confirm in patients that BIRC3 mutations confer resistance to fludarabine-based chemoimmunotherapy, a retrospective multicenter cohort of 287 untreated patients receiving first-line FCR was analyzed by targeted next-generation sequencing of 24 recurrently mutated genes in CLL. By univariate analysis adjusted for multiple comparisons BIRC3 mutations identify a poor prognostic subgroup of patients in whom FCR treatment fails (median progression-free survival: 2.2 years, P
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- 2019
163. Cystic adenomatoid malformation of the lung: clinical evolution and management.
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Bagolan, P., Nahom, A., Giorlandino, C., Trucchi, A., Bilancioni, E., Inserra, A., Gambuzza, G., and Spina, V.
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LUNG diseases , *X-rays , *EDEMA , *DIAPHRAGMATIC hernia , *DIAGNOSIS of fetal diseases , *HUMAN reproduction , *PRENATAL diagnosis , *PROGNOSIS , *RETROSPECTIVE studies , *GESTATIONAL age , *PREGNANCY outcomes , *FETAL diseases , *LUNG abnormalities , *LONGITUDINAL method , *FETAL monitoring - Abstract
Unlabelled: Cystic adenomatoid malformation of the lung (CAML) is a rare pulmonary maldevelopment resulting from an abnormal growth of the terminal bronchial structures. This study proposes a possible management of prenatally diagnosed CAML. A group of nine cases of CAML diagnosed prenatally between January 1990 and December 1995 was studied retrospectively. The evolution of lesions was followed in utero by serial ultrasound monitoring. Chest X-ray was performed at birth in all neonates and CT only in the symptomatic ones. CAML was macrocystic in three cases and microcystic in six. No polyhydramnios, hydrops or associated malformations were seen. In four cases, CAML was confirmed at birth and required surgery. The lesion decreased in size prenatally in five fetuses, of whom only one underwent surgery. In two further cases a prenatal diagnosis of CAML was changed to diaphragmatic hernia.Conclusion: Given the possible clinical disappearance or resolution of cystic adenomatoid malformation of the lung, we believe that surgery is justified at birth only in symptomatic and radiologically positive neonates. It could be safely delayed in those asymptomatic patients with either positive or negative chest X-ray. The former need computed tomography at birth, whereas, in the latter, it should be performed at 6 months of age for a more definitive assessment of the patient. [ABSTRACT FROM AUTHOR]- Published
- 1999
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164. The genetics of nodal marginal zone lymphoma
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Elisa Spaccarotella, Sakellarios Zairis, Sara Monti, Maurilio Ponzoni, Valeria Spina, Marco Paulli, Brunangelo Falini, Robin Foà, Alessio Bruscaggin, Laura Pasqualucci, Antony B. Holmes, Davide Rossi, Sabina Chiaretti, Roberto Marasca, Fary Diop, Silvia Deaglio, Michaela Cerri, Enrico Tiacci, Fabrizio Tabbò, Marco Lucioni, Monica Messina, Raul Rabadan, Luciano Cascione, Gianluca Gaidano, Antonio Ramponi, Giorgio Inghirami, Luca Arcaini, Francesco Bertoni, Hossein Khiabanian, Spina, V., Khiabanian, H., Messina, M., Monti, S., Cascione, L., Bruscaggin, A., Spaccarotella, E., Holmes, A. B., Arcaini, L., Lucioni, M., Tabbo, F., Zairis, S., Diop, F., Cerri, M., Chiaretti, S., Marasca, R., Ponzoni, M., Deaglio, S., Ramponi, A., Tiacci, E., Pasqualucci, L., Paulli, M., Falini, B., Inghirami, G., Bertoni, F., Foa, R., Rabadan, R., Gaidano, G., and Rossi, D.
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0301 basic medicine ,medicine.medical_specialty ,Cancer Research ,Proliferation index ,Lymphoma ,Immunology ,PTRD ,Receptor-Like Protein Tyrosine Phosphatases ,Splenic Neoplasm ,Marginal Zone ,Biology ,Biomarkers, Tumor ,Exome ,High-Throughput Nucleotide Sequencing ,Humans ,Lymphoma, B-Cell, Marginal Zone ,Mutation ,Receptor, Notch2 ,Receptor-Like Protein Tyrosine Phosphatases, Class 2 ,Splenic Neoplasms ,Biochemistry ,Hematology ,Cell Biology ,03 medical and health sciences ,Internal medicine ,medicine ,Splenic marginal zone lymphoma ,Exome sequencing ,Genetics ,Notch2 ,marginal zone lymphomas, PTRD, molecular profile ,Tumor ,B-Cell ,Cancer ,Class 2 ,medicine.disease ,030104 developmental biology ,Oncology ,molecular profile ,marginal zone lymphomas ,Biomarkers ,Receptor - Abstract
Nodal marginal zone lymphoma (NMZL) is a rare, indolent B-cell tumor that is distinguished from splenic marginal zone lymphoma (SMZL) by the different pattern of dissemination. NMZL still lacks distinct markers and remains orphan of specific cancer gene lesions. By combining whole-exome sequencing, targeted sequencing of tumor-related genes, whole-transcriptome sequencing, and high-resolution single nucleotide polymorphism array analysis, we aimed at disclosing the pathways that are molecularly deregulated in NMZL and we compare the molecular profile of NMZL with that of SMZL. These analyses identified a distinctive pattern of nonsilent somatic lesions in NMZL. In 35 NMZL patients, 41 genes were found recurrently affected in ≥3 (9%) cases, including highly prevalent molecular lesions of MLL2 (also known as KMT2D; 34%), PTPRD (20%), NOTCH2 (20%), and KLF2 (17%). Mutations of PTPRD, a receptor-type protein tyrosine phosphatase regulating cell growth, were enriched in NMZL across mature B-cell tumors, functionally caused the loss of the phosphatase activity of PTPRD, and were associated with cell-cycle transcriptional program deregulation and increased proliferation index in NMZL. Although NMZL shared with SMZL a common mutation profile, NMZL harbored PTPRD lesions that were otherwise absent in SMZL. Collectively, these findings provide new insights into the genetics of NMZL, identify PTPRD lesions as a novel marker for this lymphoma across mature B-cell tumors, and support the distinction of NMZL as an independent clinicopathologic entity within the current lymphoma classification.
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- 2016
165. Colorectal Cancer Stem Cells and Cell Death
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Veronica Catalano, Miriam Gaggianesi, Giorgio Stassi, Flora Iovino, Francesco Dieli, Valentina Spina, Matilde Todaro, Catalano V., Gaggianesi M., Spina V., Iovino F., Dieli F., Stassi G., and Todaro M.
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cancer stem cells ,Cancer Research ,Programmed cell death ,Colorectal cancer ,Surviving ,BMP4 ,Review ,survivin ,lcsh:RC254-282 ,Cancer stem cell ,Survivin ,medicine ,Autocrine signalling ,business.industry ,apoptosis ,Cancer ,Apoptosi ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,medicine.disease ,Oncology ,Apoptosis ,Immunology ,Cancer research ,Stem cell ,business - Abstract
Nowadays it is reported that, similarly to other solid tumors, colorectal cancer is sustained by a rare subset of cancer stem-like cells (CSCs), which survive conventional anticancer treatments, hanks to efficient mechanisms allowing escape from apoptosis, triggering tumor recurrence. To improve patient outcomes, conventional anticancer therapies have to be replaced with specific approaches targeting CSCs. In this review we provide strong support that BMP4 is an innovative therapeutic approach to prevent colon cancer growth increasing differentiation markers expression and apoptosis. Recent data suggest that in colorectal CSCs, protection from apoptosis is achieved by interleukin-4 (IL-4) autocrine production through upregulation of antiapoptotic mediators, including survivin. Consequently, IL-4 neutralization could deregulate survivin expression and localization inducing chemosensitivity of the colon CSCs pool. © 2011 by the authors; licensee MDPI, Basel, Switzerland.
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- 2011
166. The genetics of Richter syndrome reveals disease heterogeneity and predicts survival after transformation
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Luigi Maria Larocca, Valeria Spina, Marco Paulli, Julie Chang, Carlo Visco, Theodora Papadaki, Marco Lucioni, Caroline Besson, Ekaterina Chigrinova, Zijun Y. Xu-Monette, Luca Laurenti, Ken H. Young, Gianluca Gaidano, Valter Gattei, Clara Deambrogi, Roberto Marasca, Francesco Bertoni, Silvia Rasi, Davide Rossi, Kostas Stamatopoulos, Luca Arcaini, Gabrielle B. Rocque, Robin Foà, Stefano Pileri, Francesco Forconi, Rossi D, Spina V, Deambrogi C, Rasi S, Laurenti L, Stamatopoulos K, Arcaini L, Lucioni M, Rocque GB, Xu-Monette ZY, Visco C, Chang J, Chigrinova E, Forconi F, Marasca R, Besson C, Papadaki T, Paulli M, Larocca LM, Pileri SA, Gattei V, Bertoni F, Foà R, Young KH, and Gaidano G.
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p53 ,Male ,Oncology ,Chronic lymphocytic leukemia ,Cell Transformation ,Biochemistry ,Cohort Studies ,80 and over ,Multicenter Studies as Topic ,genetics ,Aged, 80 and over ,Hematology ,Adult, Aged, Aged ,80 and over, Algorithms, Cell Transformation ,Neoplastic ,genetics, Cohort Studies, Female, Genes ,genetics, Genetic Heterogeneity, Humans, Immunologic Deficiency Syndromes ,complications/diagnosis/genetics/mortality, Male, Middle Aged, Molecular Diagnostic Techniques, Multicenter Studies as Topic, Mutation ,physiology, Prognosis, Survival Analysis ,Hazard ratio ,Middle Aged ,Prognosis ,Cell Transformation, Neoplastic ,Molecular Diagnostic Techniques ,Female ,Algorithms ,Adult ,medicine.medical_specialty ,Immunology ,Context (language use) ,Richter's transformation ,Genetic Heterogeneity ,richter syndrome ,Internal medicine ,medicine ,Humans ,Survival analysis ,Aged ,business.industry ,Genetic heterogeneity ,complications/diagnosis/genetics/mortality ,Immunologic Deficiency Syndromes ,Cell Biology ,Genes, p53 ,Mutation ,Survival Analysis ,medicine.disease ,Lymphoma ,Settore MED/15 - MALATTIE DEL SANGUE ,Genes ,physiology ,Richter syndrome ,business - Abstract
Richter syndrome (RS) represents the development of diffuse large B-cell lymphoma in the context of chronic lymphocytic leukemia. The scarcity of biologic information about RS has hampered the identification of molecular predictors of RS outcome. We addressed this issue by performing a comprehensive molecular characterization of 86 pathologically proven RS. TP53 disruption (47.1%) and c-MYC abnormalities (26.2%) were the most frequent alterations, whereas common genetic lesions of de novo diffuse large B-cell lymphoma were rare or absent. By multivariate analysis, lack of TP53 disruption (hazard ratio, 0.43; P = .003) translated into significant survival advantage with 57% reduction in risk of death. An algorithm based on TP53 disruption, response to RS treatment, and Eastern Cooperative Oncology Group performance status had 80.9% probability of correctly discriminating RS survival (c-index = .809). RS that were clonally unrelated to the paired chronic lymphocytic leukemia phase were clinically and biologically different from clonally related RS because of significantly longer survival (median, 62.5 months vs 14.2 months; P = .017) and lower prevalence of TP53 disruption (23.1% vs 60.0%; P = .018) and B-cell receptor stereotypy (7.6% vs 50.0%; P = .009). The molecular dissection of RS into biologically distinct categories highlights the genetic heterogeneity of this disorder and provides clinically relevant information for refining the prognostic stratification of patients.
- Published
- 2011
167. Quaternary fault segmentation and interaction in the epicentral area of the 1561 earthquake (Mw = 6.4), Vallo di Diano, southern Apennines, Italy
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Vincenzo Spina, Giuseppe Cello, Emanuele Tondi, Paolo Galli, Stefano Mazzoli, Spina, V., Tondi, E., Galli, P., Mazzoli, Stefano, and Cello, G.
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geography ,geography.geographical_feature_category ,Pleistocene ,Magnitude (mathematics) ,Active fault ,Fault (geology) ,Tectonics ,Geophysics ,Glacial period ,Quaternary ,Geology ,Holocene ,Seismology ,Earth-Surface Processes - Abstract
The main structural characteristics of the Caggiano and Polla faults, exposed in the epicentral area of the 1561 earthquake (Mw = 6.4), southern Italy, have been investigated in detail to assess their spatial and temporal properties, and to evaluate their seismogenic potential. These right stepping normal faults show an overlap of about 7 km and an across strike separation of about 4 km. The geometric relationships between the Caggiano and Polla faults, but also the displacement distribution along each fault, demonstrate that they have been strongly interacting throughout the Pleistocene. Nevertheless, geological evidence of Holocene tectonic activity was mainly recognized along the Caggiano Fault (faulted late glacial deposits) and in the southernmost part of the Polla Fault (faulted deposits of probably Late Pleistocene age). This suggests that the Caggiano Fault can be considered as the most tectonically active fault in the Vallo di Diano Fault System. By calculating Coulomb stress changes, we have constrained modes of mechanical interactions between the two faults in a scenario compatible with the 1561 earthquake. This approach allows us to argue that both the Caggiano and the Polla Faults are probably linked at depth, and part of the same seismogenic structure which may be potentially responsible for composite ruptures with magnitude ≥ 6.5.
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- 2008
168. The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development
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Carmela Ciardullo, Sara Monti, Riccardo Dalla-Favera, Valter Gattei, Silvia Deaglio, Laura Pasqualucci, Daniela Piranda, Luca Arcaini, Vladimir Trifonov, Claudio Agostinelli, Giulia Fabbri, Fabio Facchetti, Silvia Rasi, Rosella Famà, Giorgio Inghirami, Pier Paolo Piccaluga, Gianluca Gaidano, Antony B. Holmes, Jiguang Wang, Clara Deambrogi, Roberto Serra, Francesco Bertoni, Mariangela Greco, Davide Rossi, Marco Fangazio, Fabrizio Tabbò, Andrea Rinaldi, Marco Lucioni, Robin Foà, Tiziana Vaisitti, Roberto Marasca, Raul Rabadan, Giulia Daniele, Stefania Cresta, Monica Messina, Francesca Arruga, Stefano Pileri, Alessio Bruscaggin, Silvia Franceschetti, Valeria Spina, Rossi D, Trifonov V, Fangazio M, Bruscaggin A, Rasi S, Spina V, Monti S, Vaisitti T, Arruga F, Famà R, Ciardullo C, Greco M, Cresta S, Piranda D, Holmes A, Fabbri G, Messina M, Rinaldi A, Wang J, Agostinelli C, Piccaluga PP, Lucioni M, Tabbò F, Serra R, Franceschetti S, Deambrogi C, Daniele G, Gattei V, Marasca R, Facchetti F, Arcaini L, Inghirami G, Bertoni F, Pileri SA, Deaglio S, Foà R, Dalla-Favera R, Pasqualucci L, Rabadan R, and Gaidano G.
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endocrine system diseases ,medicine.disease_cause ,0302 clinical medicine ,NOTCH2 ,immune system diseases ,hemic and lymphatic diseases ,Immunology and Allergy ,Exome ,Receptor, Notch2 ,Receptor, Notch1 ,notch2 ,next generation sequencing ,0303 health sciences ,Mutation ,B-Lymphocytes ,NF-kappa B ,Nuclear Proteins ,RNA-Binding Proteins ,Marginal zone ,DNA-Binding Proteins ,Gene Expression Regulation, Neoplastic ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Splenic Marginal Zone Lymphoma ,Signal Transduction ,endocrine system ,Lymphoma, B-Cell ,Immunology ,Notch signaling pathway ,splenic marginal zone lymphoma ,Lymphoproliferative disorders ,Biology ,Polymorphism, Single Nucleotide ,Article ,03 medical and health sciences ,medicine ,Humans ,Splenic marginal zone lymphoma ,B cell ,030304 developmental biology ,Homeodomain Proteins ,Splenic Neoplasms ,medicine.disease ,Chromatin Assembly and Disassembly ,Lymphoma ,next generation-sequencing ,Cancer research - Abstract
Notch2 mutations represent the most frequent lesion in splenic marginal zone lymphoma., Splenic marginal zone lymphoma (SMZL) is a B cell malignancy of unknown pathogenesis, and thus an orphan of targeted therapies. By integrating whole-exome sequencing and copy-number analysis, we show that the SMZL exome carries at least 30 nonsilent gene alterations. Mutations in NOTCH2, a gene required for marginal-zone (MZ) B cell development, represent the most frequent lesion in SMZL, accounting for ∼20% of cases. All NOTCH2 mutations are predicted to cause impaired degradation of the NOTCH2 protein by eliminating the C-terminal PEST domain, which is required for proteasomal recruitment. Among indolent B cell lymphoproliferative disorders, NOTCH2 mutations are restricted to SMZL, thus representing a potential diagnostic marker for this lymphoma type. In addition to NOTCH2, other modulators or members of the NOTCH pathway are recurrently targeted by genetic lesions in SMZL; these include NOTCH1, SPEN, and DTX1. We also noted mutations in other signaling pathways normally involved in MZ B cell development, suggesting that deregulation of MZ B cell development pathways plays a role in the pathogenesis of ∼60% SMZL. These findings have direct implications for the treatment of SMZL patients, given the availability of drugs that can target NOTCH, NF-κB, and other pathways deregulated in this disease.
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- 2012
169. Suppressor of cytokine signaling 3 sensitizes anaplastic thyroid cancer to standard chemotherapy
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Francesco Dieli, Giuseppe Buscemi, Ruggero De Maria, Vincenzo Eterno, Maria Giovanna Francipane, Miriam Bini, Gaspare Gulotta, Matilde Todaro, Giorgio Stassi, Gregorio Scerrino, Valentina Spina, Francipane, MG, Eterno, V, Spina, V, Bini, M, Scerrino, G, Buscemi, G, Gulotta, G, Todaro, M, Dieli, F, De Maria, R, and Stassi, G
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STAT3 Transcription Factor ,Cancer Research ,Oncology ,Down-Regulation ,Mice, Nude ,Suppressor of Cytokine Signaling Proteins ,thyroid,cancer spheres, cytokines, apoptosis, chemoterapy ,Mice ,Phosphatidylinositol 3-Kinases ,Suppressor of Cytokine Signaling 1 Protein ,Medicine ,Animals ,Humans ,SOCS3 ,Thyroid Neoplasms ,Anaplastic thyroid cancer ,Phosphorylation ,Thyroid cancer ,PI3K/AKT/mTOR pathway ,Aged ,Settore MED/04 - Patologia Generale ,Janus kinase 1 ,business.industry ,Suppressor of cytokine signaling 1 ,Settore BIO/16 - Anatomia Umana ,Gene Transfer Techniques ,Cancer ,Janus Kinase 1 ,Middle Aged ,medicine.disease ,Xenograft Model Antitumor Assays ,Settore MED/18 - Chirurgia Generale ,Drug Resistance, Neoplasm ,Suppressor of Cytokine Signaling 3 Protein ,Immunology ,Cancer research ,Female ,business ,Janus kinase ,STAT6 Transcription Factor ,Proto-Oncogene Proteins c-akt - Abstract
We previously showed that cancer cells from papillary, follicular, and anaplastic thyroid carcinomas produce interleukin-4 and interleukin-10, which counteract the cytotoxic activity of conventional chemotherapy through the up-regulation of antiapoptotic molecules. Here, we identify Janus kinase/signal transducers and activators of transcription (STAT) and phosphatidyl inositol 3-kinase (PI3K)/AKT as the down-stream pathways through which these cytokines confer resistance to cell death in thyroid cancer. We found that the absence of suppressors of cytokine signaling (SOCS) molecules allows the propagation of the survival signaling. Exogenous expression of SOCS1, SOCS3, and SOCS5 in the highly aggressive anaplastic thyroid cancer cells reduces or abolishes STAT3 and 6 phosphorylation and PI3K/Akt pathway activation resulting in alteration in the balance of proapoptotic and antiapoptotic molecules and sensitization to chemotherapeutic drugs in vitro. Likewise, exogenous expression of SOCS3 significantly reduces tumor growth and potently enhances the efficacy of chemotherapy in vivo. Our results indicate that SOCS3 regulation of cytokines-prosurvival programs might represent a new strategy to overcome the resistance to chemotherapy-induced cell death of thyroid cancer. We previously showed that cancer cells from papillary, follicular, and anaplastic thyroid carcinomas produce interleukin-4 and interleukin-10, which counteract the cytotoxic activity of conventional chemotherapy through the up-regulation of antiapoptotic molecules. Here, we identify Janus kinase/signal transducers and activators of transcription (STAT) and phosphatidyl inositol 3-kinase (PI3K)/AKT as the down-stream pathways through which these cytokines confer resistance to cell death in thyroid cancer. We found that the absence of suppressors of cytokine signaling (SOCS) molecules allows the propagation of the survival signaling. Exogenous expression of SOCS1, SOCS3, and SOCS5 in the highly aggressive anaplastic thyroid cancer cells reduces or abolishes STAT3 and 6 phosphorylation and PI3K/Akt pathway activation resulting in alteration in the balance of proapoptotic and antiapoptotic molecules and sensitization to chemotherapeutic drugs in vitro. Likewise, exogenous expression of SOCS3 significantly reduces tumor growth and potently enhances the efficacy of chemotherapy in vivo. Our results indicate that SOCS3 regulation of cytokines-prosurvival programs might represent a new strategy to overcome the resistance to chemotherapy-induced cell death of thyroid cancer.
- Published
- 2009
170. TP53 Mutations, the Most Frequent Genetic Lesion in Richter Syndrome, Represent An Independent Predictor of Survival Post Transformation
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Marco Lucioni, Valeria Spina, Marco Paulli, Francesco Bertoni, Ekaterina Chigrinova, Gianluca Gaidano, Julie E. Chang, Caroline Besson, Josep F. Nomdedeu, Davide Rossi, Gabrielle B. Rocque, Vincenzo Canzonieri, Francesco Forconi, Roberto Marasca, Luca Arcaini, Clara Deambrogi, Valter Gattei, Ken H. Young, Jeffrey T. Malik, Rossi, D, Spina, V, Deambrogi, C, Lucioni, M, Arcaini, L, Rocque, Gb, Malik, Jt, Chang, Je, Chigrinova, E, Nomdedeu, Jf, Forconi, F, Marasca, R, Besson, C, Canzonieri, V, Paulli, M, Gattei, V, Bertoni, F, Young, Kh, and Gaidano, G
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medicine.medical_specialty ,Pathology ,business.industry ,Chronic lymphocytic leukemia ,Immunology ,Cancer ,Aggressive lymphoma ,Cell Biology ,Hematology ,medicine.disease ,BCL6 ,Biochemistry ,Gastroenterology ,Lymphoma ,B symptoms ,hemic and lymphatic diseases ,Internal medicine ,medicine ,Stage (cooking) ,medicine.symptom ,business ,Diffuse large B-cell lymphoma - Abstract
Abstract 670 Richter syndrome (RS) represents the transformation of chronic lymphocytic leukemia (CLL) to aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL). Knowledge of the genetic lesions associated with RS is scant and represents the aim of this study. The study was based on 47 RS cases (all DLBCL). In 32 cases, paired CLL/RS samples were available (28 clonally related and 4 clonally unrelated). In 15 cases, the sole RS sample was analysed. According to CD10/BCL6/MUM1 immunohistochemistry expression pattern, 43/47 (91.5%) RS were classified as non-germinal center DLBCL. At diagnosis, 37.8% RS showed ECOG PS >1, 77.8% Binet stage B-C, 95.7% Ann Arbor stage III-IV, 44.4% B symptoms, 45.7% tumor size >5 cm, 32.6% involvement of >1 extranodal site, 66.7% LDH elevation, and 28.9% platelets Disclosures: No relevant conflicts of interest to declare.
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- 2009
171. High density genome-wide DNA profiling reveals a remarkably stable profile in hairy cell leukaemia
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Francesco Bertoni, Daniela Capello, Gianluca Gaidano, Ivo Kwee, Francesco Lauria, Donatella Raspadori, Paola M.V. Rancoita, Francesco Forconi, Emanuele Zucca, Davide Rossi, Andrea Rinaldi, Giulia Poretti, Valeria Spina, Elisa Sozzi, Forconi, F, Poretti, G, Kwee, I, Sozzi, E, Rossi, D, Rancoita, PAOLA MARIA VITTORIA, Capello, D, Rinaldi, A, Zucca, E, Raspadori, D, Spina, V, Lauria, F, Gaidano, G, and Bertoni, F.
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Adult ,Male ,Hairy Cell ,Loss of Heterozygosity ,Adult, Aged, DNA Fingerprinting ,methods, DNA ,Neoplasm ,genetics, Female, Fibroblast Growth Factors ,biosynthesis/genetics, Genome ,Human, Humans, Immunophenotyping, Leukemia ,genetics/immunology/metabolism, Loss of Heterozygosity, Male, Middle Aged, Neoplasm Proteins ,biosynthesis/genetics, Oligonucleotide Array Sequence Analysis ,methods, Reverse Transcriptase Polymerase Chain Reaction ,methods ,biosynthesis/genetics ,Biology ,Genome ,Immunophenotyping ,Loss of heterozygosity ,medicine ,Humans ,Hairy cell leukemia ,genetics ,Gene ,Aged ,Oligonucleotide Array Sequence Analysis ,Genetics ,Leukemia, Hairy Cell ,Leukemia ,Genome, Human ,Reverse Transcriptase Polymerase Chain Reaction ,DNA, Neoplasm ,Hematology ,DNA ,Middle Aged ,medicine.disease ,Molecular biology ,DNA Fingerprinting ,Uniparental disomy ,Neoplasm Proteins ,Fibroblast Growth Factors ,genetics/immunology/metabolism ,DNA profiling ,Female ,Comparative genomic hybridization ,Human - Abstract
Hairy cell leukaemia (HCL) is a rare B-cell neoplasm for which the molecular mechanisms are largely unknown. High-density genome-wide DNA profiling was performed with Affymetrix 250K arrays to analyse copy number (CN) changes and loss of heterozygosity (LOH) in 16 cases of HCL. Four of 16 cases (25%) demonstrated gross non-recurrent CN deletions. Within the affected regions, we identified genes involved in bone marrow fibrosis (FGF12) and response to treatment (TP53) in individual cases. Large regions (> 5 Mb) of LOH without any concomitant DNA CN changes were identified in 5/16 (31%) HCL and were indicative of uniparental disomy UD. The germline origin of UD was demonstrated in one case for which a matched normal sample was available. Overall analysis of LOH showed that identical loci were recurrently targeted in chromosomes 1, 2 and 6. As a whole, however, HCL showed a remarkably stable genome. This finding adds to several other features that are unique to HCL among mature B-cell tumours.
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- 2008
172. Spontaneous Pregnancy after 4D-Hysterosalpingo-Sonography (HyCoSy) in the Same Menstrual Cycle: A Case Report and an Updating Review of the Current Literature regarding the Positive Impact of Tubal Flushing Effect on Fertility.
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Bisogni F, Galanti F, Riccio S, Ghanitab S, Polletta S, Annesi V, Antonaci D, Rago A, Schiavi MC, Spina V, and Rago R
- Abstract
Infertility is increasing worldwide, as well as in Italy, and fallopian tube pathology represents one of the most impacting causes of infertility for multiple women. Indeed, tubal patency assessment is a crucial step in medical evaluation for women attending an in vitro fertilization (IVF) center. Currently, different methods for tubal investigation are available, such as chromosalpingoscopy, hysterosalpingography (HSG), and hysterosalpingo-contrast sonography (HyCoSy). This diagnostic exam is performed by ultrasonography and an air-water-based contrast agent represented by air-water, or foam solution (HyFoSy). An additional side benefit of these assessment tests is a fertility-enhancing effect, thanks to a positive effect defined as "tubal flushing," which in current literature is more strongly associated with HyFoSy with respect to HyCoSy. In this report, we present a case of a 34-year-old woman presented to our attention at the Reproductive and Physiopathology Unit of Sandro Pertini Hospital, Rome, in 2023, with unexplained infertility for 3.1 years of free sexual intercourse with a partner who did not report sperm abnormalities. Subsequently, in this exam, the woman spontaneously conceived in the same menstrual cycle that the 4D-HyCoSy was performed, without any additional fertility enhancement interventions. In this case report, we also include an updating review of the current literature regarding the insurgence of spontaneous pregnancy after this technique in order to explore the physiopathological and etiopathogenetic mechanisms underlying the achievement of spontaneous pregnancy and to confront our case with other recent works published. According to our clinical experience and the current literature, 4D-HyCoSy is the easiest, safest, and cheapest diagnostic exam for investigating tubal patency, which can lead to medical success in some cases of "unexplained infertility" as the achievement of a spontaneous pregnancy., Competing Interests: All authors declare no conflict of interest., (Copyright © 2024 Francesco Bisogni et al.)
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- 2024
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173. How much should we sequence? An analysis of the Swiss SARS-CoV-2 surveillance effort.
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Wegner F, Cabrera-Gil B, Tanguy A, Beckmann C, Beerenwinkel N, Bertelli C, Carrara M, Cerutti L, Chen C, Cordey S, Dumoulin A, du Plessis L, Friedli M, Gerth Y, Greub G, Härri A, Hirsch H, Howald C, Huber M, Imhof A, Kaiser L, Kufner V, Leib SL, Leuzinger K, Lleshi E, Martinetti G, Mäusezahl M, Moraz M, Neher R, Nolte O, Ramette A, Redondo M, Risch L, Rohner L, Roloff T, Schläepfer P, Schneider K, Singer F, Spina V, Stadler T, Studer E, Topolsky I, Trkola A, Walther D, Wohlwend N, Zehnder C, Neves A, and Egli A
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- Humans, Switzerland epidemiology, Epidemiological Monitoring, Pandemics, Phylogeny, COVID-19 epidemiology, COVID-19 virology, COVID-19 diagnosis, SARS-CoV-2 genetics, SARS-CoV-2 isolation & purification, SARS-CoV-2 classification, Genome, Viral genetics
- Abstract
During the SARS-CoV-2 pandemic, many countries directed substantial resources toward genomic surveillance to detect and track viral variants. There is a debate over how much sequencing effort is necessary in national surveillance programs for SARS-CoV-2 and future pandemic threats. We aimed to investigate the effect of reduced sequencing on surveillance outcomes in a large genomic data set from Switzerland, comprising more than 143k sequences. We employed a uniform downsampling strategy using 100 iterations each to investigate the effects of fewer available sequences on the surveillance outcomes: (i) first detection of variants of concern (VOCs), (ii) speed of introduction of VOCs, (iii) diversity of lineages, (iv) first cluster detection of VOCs, (v) density of active clusters, and (vi) geographic spread of clusters. The impact of downsampling on VOC detection is disparate for the three VOC lineages, but many outcomes including introduction and cluster detection could be recapitulated even with only 35% of the original sequencing effort. The effect on the observed speed of introduction and first detection of clusters was more sensitive to reduced sequencing effort for some VOCs, in particular Omicron and Delta, respectively. A genomic surveillance program needs a balance between societal benefits and costs. While the overall national dynamics of the pandemic could be recapitulated by a reduced sequencing effort, the effect is strongly lineage-dependent-something that is unknown at the time of sequencing-and comes at the cost of accuracy, in particular for tracking the emergence of potential VOCs.IMPORTANCESwitzerland had one of the most comprehensive genomic surveillance systems during the COVID-19 pandemic. Such programs need to strike a balance between societal benefits and program costs. Our study aims to answer the question: How would surveillance outcomes have changed had we sequenced less? We find that some outcomes but also certain viral lineages are more affected than others by sequencing less. However, sequencing to around a third of the original effort still captured many important outcomes for the variants of concern such as their first detection but affected more strongly other measures like the detection of first transmission clusters for some lineages. Our work highlights the importance of setting predefined targets for a national genomic surveillance program based on which sequencing effort should be determined. Additionally, the use of a centralized surveillance platform facilitates aggregating data on a national level for rapid public health responses as well as post-analyses., Competing Interests: The authors declare no conflict of interest.
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- 2024
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174. Minimally Invasive Treatment of Stress Urinary Incontinence in Women: A Prospective Comparative Analysis between Bulking Agent and Single-Incision Sling.
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Campanella L, Gabrielli G, Chiodo E, Stefanachi V, Pennacchini E, Grilli D, Grossi G, Cignini P, Morciano A, Zullo MA, Palazzetti P, Rappa C, Calcagno M, Spina V, Cervigni M, and Schiavi MC
- Abstract
Introduction: The study aims to compare the efficacy and safety of bulking agents and single-incision slings in the treatment of urinary incontinence in 159 patients during a 29-month follow-up period., Material and Methods: Of the 159 patients suffering from stress urinary incontinence, 64 were treated with bulking agents (PAHG Bulkamid
® ) and 75 with a single-incision sling (Altis® ). The ICIQ-UI-SF (Incontinence Questionnaire-Urine Incontinence-Short Form), PISQ-12 (Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaires short form), FSFI (Female Sexual Function Index), FSDS (Female Sexual Distress Scale), and PGI-I (Patient Global Improvement Index) were used to assess efficiency and quality of life., Results: The bulking agents showed high efficacy and safety during the 29-month follow-up. Post-operative complications were recorded in both groups, with only two significant differences. The Bulkamid group experienced no pain, while 10.8% of the ALTIS group experienced groin pain and 5% experienced de novo urgency. Furthermore, patients treated with bulking agents experienced reduced nicturia (0.78 vs. 0.92 in patients treated with single-incision slings.). In both groups, we noticed a significant improvement in QoL (quality of life), with a halved ICIQ-UI-SF (International Consultation on Incontinence Questionnaire-Urine Incontinence-Short Form) score which was completed to assess the impact of urine symptoms. After 24 months of therapy, the Bulkamid group saw a decrease from 14.58 ± 5.11 at baseline to 5.67 ± 1.90 ( p < 0.0001), whereas the ALTIS group experience a decrease from 13.75 ± 5.89 to 5.83 ± 1.78. Similarly, we observed an improvement in sexual function, with the number of sexually active patients increasing from 29 to 44 (56.4%) in the Bulkamid group ( p = 0.041) and from 31 to 51 (61.7%) in the ALTIS group ( p = 0.034). According to the most recent statistics, the PISQ-12, FSFI, and FSDS scores all demonstrated an improvement in women's sexual function., Conclusions: In terms of efficacy and safety, bulking agents had notable results over the 29-month follow-up period. Furthermore, the patients treated with bulking agents reported a lower incidence of postoperative complications and a no discernible difference in terms of quality of life and sexual activity compared to the ones treated with single-incision slings. Bulking agents can be considered a very reliable therapeutic option based on accurate patient selection.- Published
- 2024
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175. Sequential combined approach in patients with mixed urinary incontinence: surgery followed by posterior tibial nerve stimulation.
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Carletti V, Yacoub V, Grilli D, Morgani C, Palazzetti PL, Zullo MA, Luffarelli P, Valensise HC, Maneschi F, Spina V, and Schiavi MC
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- Humans, Female, Middle Aged, Aged, Quality of Life, Retrospective Studies, Treatment Outcome, Urinary Incontinence, Urge surgery, Tibial Nerve, Urinary Incontinence, Stress surgery, Urinary Incontinence
- Abstract
Background: The aim of the study was to demonstrate the efficacy of sequential combined treatment with transobturator tape (TOT) followed by posterior tibial nerve stimulation (PTNS) in patients with mixed urinary incontinence (MUI); quality of life and patients' satisfaction was also assessed., Methods: Retrospective analysis on women affected by MUI with prevalent Stress Urinary Incontinence (SUI) component. Women, divided in 2 groups, underwent different treatments, TOT vs. TOT+PTNS. Population was assessed by medical history, previous pelvic surgery, clinical exam, urodynamic exams, pelvic ultrasound examination, and questionnaires (The International Consultation on Incontinence Questionnaire Short Form, Overactive Bladder Questionnaire, Health Related Quality of Life) comparing them before and after 12 weeks after treatment., Results: One hundred twelve women were enrolled in the study. The mean age was 57.96±7.34 in the first group (N.=60) and 58.29±6.14 in the second group (N.=52). Peak flow (mL/s) statistically improved after treatment, 22.23±4.29 (TOT) vs. 24.81±5.8 (TOT+PTNS). First voiding desire (mL) improved significantly between the two groups 108.72±19.24 vs. 142.43±19.98. Maximum cystometric capacity (mL) in the TOT group at 12-weeks was 328.76±82.44 vs. TOT+PTNS group of 396.26±91.21. Detrusor pressure at peak flow(cmH2O) showed a greater improvement in TOT+PTNS than TOT alone 14.45±6.10 vs. 11.89±54.49. At 12-week, urinary diary and quality of life improved in terms of urgent urination events, mean number of voids, urge symptoms and nocturia events. The Patient Impression of Global Improvement (PGI-I) after 3 months was better in combined group., Conclusions: Combined and sequential TOT+PTNS is more effective compared to TOT alone in MUI patients with prevalent SUI component.
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- 2024
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176. Neurophysiological underpinnings of an intensive protocol for upper limb motor recovery in subacute and chronic stroke patients.
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Lassi M, Dalise S, Bandini A, Spina V, Azzollini V, Vissani M, Micera S, Mazzoni A, and Chisari C
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- Humans, Activities of Daily Living, Prospective Studies, Upper Extremity, Recovery of Function physiology, Treatment Outcome, Stroke Rehabilitation methods, Stroke
- Abstract
Background: Upper limb (UL) motor impairment following stroke is a leading cause of functional limitations in activities of daily living. Robot-assisted therapy supports rehabilitation, but how its efficacy and the underlying neural mechanisms depend on the time after stroke is yet to be assessed., Aim: We investigated the response to an intensive protocol of robot-assisted rehabilitation in sub-acute and chronic stroke patients, by analyzing the underlying changes in clinical scores, electroencephalography (EEG) and end-effector kinematics. We aimed at identifying neural correlates of the participants' upper limb motor function recovery, following an intensive 2-week rehabilitation protocol., Design: Prospective cohort study., Setting: Inpatients and outpatients from the Neurorehabilitation Unit of Pisa University Hospital, Italy., Population: Sub-acute and chronic stroke survivors., Methods: Thirty-one stroke survivors (14 sub-acute, 17 chronic) with mild-to-moderate UL paresis were enrolled. All participants underwent ten rehabilitative sessions of task-oriented exercises with a planar end-effector robotic device. All patients were evaluated with the Fugl-Meyer Assessment Scale and the Wolf Motor Function Test, at recruitment (T0), end-of-treatment (T1), and one-month follow-up (T2). Along with clinical scales, kinematic parameters and quantitative EEG were collected for each patient. Kinematics metrics were related to velocity, acceleration and smoothness of the movement. Relative power in four frequency bands was extracted from the EEG signals. The evolution over time of kinematic and EEG features was analyzed, in correlation with motor recovery., Results: Both groups displayed significant gains in motility after treatment. Sub-acute patients displayed more pronounced clinical improvements, significant changes in kinematic parameters, and a larger increase in Beta-band in the motor area of the affected hemisphere. In both groups these improvements were associated to a decrease in the Delta-band of both hemispheres. Improvements were retained at T2., Conclusions: The intensive two-week rehabilitation protocol was effective in both chronic and sub-acute patients, and improvements in the two groups shared similar dynamics. However, stronger cortical and behavioral changes were observed in sub-acute patients suggesting different reorganizational patterns., Clinical Rehabilitation Impact: This study paves the way to personalized approaches to UL motor rehabilitation after stroke, as highlighted by different neurophysiological modifications following recovery in subacute and chronic stroke patients.
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- 2024
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177. Distinct Hodgkin lymphoma subtypes defined by noninvasive genomic profiling.
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Alig SK, Shahrokh Esfahani M, Garofalo A, Li MY, Rossi C, Flerlage T, Flerlage JE, Adams R, Binkley MS, Shukla N, Jin MC, Olsen M, Telenius A, Mutter JA, Schroers-Martin JG, Sworder BJ, Rai S, King DA, Schultz A, Bögeholz J, Su S, Kathuria KR, Liu CL, Kang X, Strohband MJ, Langfitt D, Pobre-Piza KF, Surman S, Tian F, Spina V, Tousseyn T, Buedts L, Hoppe R, Natkunam Y, Fornecker LM, Castellino SM, Advani R, Rossi D, Lynch R, Ghesquières H, Casasnovas O, Kurtz DM, Marks LJ, Link MP, André M, Vandenberghe P, Steidl C, Diehn M, and Alizadeh AA
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- Humans, Mutation, Reed-Sternberg Cells metabolism, Tumor Microenvironment, Single-Cell Gene Expression Analysis, Genomics, Hodgkin Disease blood, Hodgkin Disease classification, Hodgkin Disease diagnosis, Hodgkin Disease genetics, Circulating Tumor DNA blood, Circulating Tumor DNA genetics, Genome, Human genetics
- Abstract
The scarcity of malignant Hodgkin and Reed-Sternberg cells hampers tissue-based comprehensive genomic profiling of classic Hodgkin lymphoma (cHL). By contrast, liquid biopsies show promise for molecular profiling of cHL due to relatively high circulating tumour DNA (ctDNA) levels
1-4 . Here we show that the plasma representation of mutations exceeds the bulk tumour representation in most cases, making cHL particularly amenable to noninvasive profiling. Leveraging single-cell transcriptional profiles of cHL tumours, we demonstrate Hodgkin and Reed-Sternberg ctDNA shedding to be shaped by DNASE1L3, whose increased tumour microenvironment-derived expression drives high ctDNA concentrations. Using this insight, we comprehensively profile 366 patients, revealing two distinct cHL genomic subtypes with characteristic clinical and prognostic correlates, as well as distinct transcriptional and immunological profiles. Furthermore, we identify a novel class of truncating IL4R mutations that are dependent on IL-13 signalling and therapeutically targetable with IL-4Rα-blocking antibodies. Finally, using PhasED-seq5 , we demonstrate the clinical value of pretreatment and on-treatment ctDNA levels for longitudinally refining cHL risk prediction and for detection of radiographically occult minimal residual disease. Collectively, these results support the utility of noninvasive strategies for genotyping and dynamic monitoring of cHL, as well as capturing molecularly distinct subtypes with diagnostic, prognostic and therapeutic potential., (© 2023. The Author(s), under exclusive licence to Springer Nature Limited.)- Published
- 2024
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178. XPO1 mutations identify early-stage CLL characterized by shorter time to first treatment and enhanced BCR signalling.
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Moia R, Terzi di Bergamo L, Talotta D, Bomben R, Forestieri G, Spina V, Bruscaggin A, Cosentino C, Almasri M, Dondolin R, Bittolo T, Zucchetto A, Baldoni S, Del Giudice I, Mauro FR, Maffei R, Chiarenza A, Tafuri A, Laureana R, Del Principe MI, Zaja F, D'Arena G, Olivieri J, Rasi S, Mahmoud A, Al Essa W, Awikeh B, Kogila S, Bellia M, Mouhssine S, Sportoletti P, Marasca R, Scarfò L, Ghia P, Gattei V, Foà R, Rossi D, and Gaidano G
- Abstract
Here we evaluated the epigenomic and transcriptomic profile of XPO1 mutant chronic lymphocytic leukaemia (CLL) and their clinical phenotype. By ATAC-seq, chromatin regions that were more accessible in XPO1 mutated CLL were enriched of binding sites for transcription factors regulated by pathways emanating from the B-cell receptor (BCR), including NF-κB signalling, p38-JNK and RAS-RAF-MEK-ERK. XPO1 mutant CLL, consistent with the chromatin accessibility changes, were enriched with transcriptomic features associated with BCR and cytokine signalling. By combining epigenomic and transcriptomic data, MIR155HG, the host gene of miR-155, and MYB, the transcription factor that positively regulates MIR155HG, were upregulated by RNA-seq and their promoters were more accessible by ATAC-seq. To evaluate the clinical impact of XPO1 mutations, we investigated a total of 957 early-stage CLL subdivided into 3 independent cohorts (N = 276, N = 286 and N = 395). Next-generation sequencing analysis identified XPO1 mutations as a novel predictor of shorter time to first treatment (TTFT) in all cohorts. Notably, XPO1 mutations maintained their prognostic value independent of the immunoglobulin heavy chain variable status and early-stage prognostic models. These data suggest that XPO1 mutations, conceivably through increased miR-155 levels, may enhance BCR signalling leading to higher proliferation and shorter TTFT in early-stage CLL., (© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.)
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- 2023
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179. Iodized Salt May Not Be Sufficient to Guarantee an Adequate Iodine Intake in Pregnant Women.
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Spina V, Baldini E, Cardarelli S, Oliva C, Venarubea S, Faraoni F, Pastore G, Tittoni R, Musella A, Squarcella A, Lori E, Renzi E, Feroci R, Mastrodonato F, Ciferri F, Virili C, Centanni M, Fabiani C, Rago R, Schiavi MC, Palazzetti P, D'Armiento E, Cantisani V, Sorrenti S, and Ulisse S
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- Female, Humans, Pregnancy, Nutritional Status, Thyroid Gland, Sodium Chloride, Dietary, Thyroid Hormones, Pregnant Women, Iodine
- Abstract
Adequate iodine intake is of crucial importance in pregnancy to meet the thyroid hormone needs of both mother and fetus. In the present study, undertaken as a part of the surveillance actions following the introduction in Italy of a national salt iodination program in 2005, the iodine intake was investigated in 123 pregnant women and 49 control women living in the same area of central Italy. All the participants were screened for urinary iodine concentration (UIC), serum level of thyrotropin, free-thyroxine, free-triiodothyronine, and thyroid volume. Moreover, they were provided with a questionnaire on the use of iodine-containing salt or supplements. Control women had a median UIC of 102 µg/L, consistent with an iodine sufficiency, while in pregnant women the median UIC value was 108 µg/L, lower than the endorsed UIC of 150 µg/L. In addition, pregnant women showed a significantly increased median thyroid volume compared to controls. Interestingly, the median UIC did not differ between pregnant women not using iodine-containing salt or supplements and those regularly consuming iodized salt alone, while pregnant women with a daily intake of iodine-containing supplements had an adequate median UIC (168 µg/L). In conclusion, the data reported here showed that pregnant women and their fetuses are still exposed to the detrimental effects of iodine deficiency and that the consumption of iodine-containing supplements should be recommended in pregnancy.
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- 2023
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180. Menstrual cycle alterations in reproductive age women after anti COVID-19 vaccination. A survey in 419 Italian women and quality of life and sexual function evaluation.
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Loggia M, DI Pinto A, Morgani C, Cardella G, Contadini A, Palazzetti PL, Macrì F, Moro PR, Spina V, Morciano A, Valensise HC, and Schiavi MC
- Abstract
Background: Pharmacovigilance agencies did not collect data regarding menstrual changes after COVID-19 vaccination even if many women experienced it. Our aim was to evaluate whether COVID-19 vaccination is associated with secondary changes in menstrual cycle and to assess both quality of life (QoL) and sexual function (SF)., Methods: This study is a retrospective analysis referred to our Department from January 2021 to December 2021. The study cohort responded to same questionnaires before the second dose of vaccination (referring to previous 3 months) and 3 months after that (referring to three menstrual cycles after full-dose vaccination). The surveys administered were FSFI, FSDS, SF-36, MEDI-Q and the VAS-scale for dysmenorrhea., Results: Four-hundred-nineteen vaccinated women were included in the study. The survey did not show a significant change in menstrual cycle length before and after COVID-19 vaccine (5.88±3.67 vs. 4.97±2.89, P=0.21); the interval between periods was significantly higher after a full-cycle vaccination (28.32±7.34 vs. 32.38±7.45, P<0.02); 32 patients (7.6%) developed amenorrhea after the second dose; VAS Scale did not change significantly (median range 3 (3-5) vs. 4 (3-6), P=0.20). MEDI-Q did not show significant variations before and after the vaccination (43.21±11.65 vs. 40.28±9.88, P=0.35). QoL and SF did not change significantly (FSFI median 27 [24-29] vs. 28 [25-30], P=0.12, FSDS median 9 [5-11] vs. 8 [4-12], P=0.22), SF-36 median 81 [70-85] vs. 82 [72-86], P=0.43)., Conclusions: COVID-19 vaccination is associated with a significant change in intervals between menstrual cycles without other alterations in menstrual characteristics, in QoL or SF.
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- 2023
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181. Quality of life and sexual function evaluation in women with urogynecological diseases analyzed with telemedicine during the COVID-19 period: the beginning of a new era?
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Schiavi MC, Morgani C, Grilli D, Yacoub V, Carletti V, Zullo MA, Luffarelli P, Valensise HC, Rappa C, Spina V, Palazzetti PL, and Cervigni M
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- Humans, Female, Quality of Life, Sexual Behavior, Surveys and Questionnaires, Urinary Bladder, Overactive complications, COVID-19 therapy
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Background: The aim of this study was to demonstrate that the implementation of remote medical care in the management of patients suffering from specific urogynecological diseases can be a valid alternative to outpatient visits leading to a huge saving of resources which can be used for real emergencies. Therefore, the primary aim of this study was to demonstrate that patients treated with telehealth had the same improvement in symptoms and Quality of Life as those treated with outpatient visits., Methods: Observational analysis on women with urogynecological diseases was performed during restrictive measures period. One group of patients was assessed in the clinic and one group by video consultations. The population answered Female Sexual Function Index (FSFI), Female Sexual Distress Scale (FSDS), the Overactive Bladder Questionnaire Symptoms and Health-Related Quality of Life Short-Form Symptoms (OAB-Q), Prolapse Quality of Life Questionnaire (P-QoL), the Pelvic Pain and Urinary/Frequency Patient Symptom Scale (PUF) scores, the Short Form Health Survey questionnaires (SF-36) during the first visit and after 12 weeks. The primary endpoint was to evaluate the change in symptoms after the outpatient and telemedicine visit. The secondary endpoint was the evaluation of the telemedicine impact on the Quality of Life and sexual function., Results: One hundred twenty-five patients were considered. Symptoms of overactive bladder, genitourinary syndrome, and recurrent urinary infections improved significantly in both groups with no significant differences. Sexual activity increased significantly in both groups with a significant change in FSFI and FSDS values. The SF-36 showed a significant change 12 weeks after the visit in both groups., Conclusions: Telemedicine is equally useful and effective as the outpatient visits in patients suffering from urogynecological diseases.
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- 2023
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182. Combined treatment with vaginal native tissue repair plus mid-urethral sling or pelvic floor muscle training in patients with anterior defect and occult stress urinary incontinence: quality of life and sexual function analysis.
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Grilli D, Loggia M, Sala F, Palazzetti PL, Zullo MA, Luffarelli P, Spina V, Valensise HC, and Schiavi MC
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Background: The aim of this study was to compare the efficacy of vaginal native tissue repair (VNTR) combined with tension-free transobturator tape (TVT-O) or pelvic floor muscle training (PFMT) in terms of quality of life (QoL) and sexual function (SF) in women affected by anterior defect and occult stress urinary incontinence (OSUI)., Methods: One hundred forty-seven patients with symptomatic anterior defect with OSUI underwent VNTR. In 71 patients TVT-O was inserted and 76 underwent PFMT after surgery. Clinical exam, 3-day voiding diary and urodynamic testing were evaluated in preoperative and postoperative times. Specific questionnaires were also administered, in order to indagate disease perception and the impact on QoL and SF., Results: Nine patients had postoperative pain in the TVT-O group vs. 0 patients in the PMFT group (P=0.001) and 7 patients reported de novo urgency vs. 3 in the two groups, respectively. At 12 weeks follow-up (FU), the first voiding desire was at 88.12+19.70 mL in VNTR+TOT vs. 102.29+19.13 (P=0.03); the mean number of voids (24 hours) was 9.95±2.66 vs. 6.14±1.77 (P=0.04), respectively. No significant differences in terms of QoL and SF were shown., Conclusions: This retrospective study suggests that VNTR+TVT-O and VNTR+PMFT have the same efficacy in terms of QoL and SF, with several post-operative complications, even if minor, in patients treated with combined surgery.
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- 2023
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183. Evaluation of the efficacy and safety of single incision sling vs TVT-O in obese patients with stress urinary incontinence: Quality of life and sexual function analysis.
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Schiavi MC, Carletti V, Yacoub V, Cardella G, Luffarelli P, Valensise HCC, Palazzetti P, Spina V, and Zullo MA
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- Humans, Female, Treatment Outcome, Quality of Life, Postoperative Complications epidemiology, Postoperative Complications etiology, Urinary Incontinence, Stress surgery, Suburethral Slings adverse effects
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Objectives: The aim of the study is to demonstrate the best stress urinary incontinence (SUI) surgical technique for women with a Body mass index higher than 30. The results of Transvaginal Tension Free Vaginal Tape-Obturator and Mini-sling surgery were analyzed and compared through both clinical examination and standardized questionnaires at 36 months of follow-up., Materials and Methods: This is a retrospective multicenter study over 159 women with SUI who underwent surgery. Seventy-eight women underwent TVT-O and 81 Mini-sling technique. Intra and post-operative complications were recorded. Patients were monitored for 36 months by analyzing symptoms, voiding diary, quality of life and sexual activity through standardized questionnaires., Results: Complications had a low incidence in both groups and inter-group differences were superimposable. Only groin pain was statistically higher after TVT-O than after Mini-sling (12.8% vs1.2%, p = 0.03). At 36 months of follow-up, a statistically significant decrease in Positive stress test (%) and Q-Tip test (grade) was observed in both groups with no differences between them (p = 0.54 and p = 0.32 respectively). The mean number of daily voids was higher after TVT-O (p = 0.04) than after Altis (p = 0.22) with a significant difference in favor of the Altis group (p = 0.03). After 36 months, there were no significant differences between groups in terms of quality of life and sexual activity. PGI-I did not show any difference between groups (p = 0.21)., Conclusion: TVT-O and Minisling had the same efficacy and results in the surgical treatment of SUI in obese women. Both techniques relieved their symptoms and improved their quality of life without any significant difference except for a lower incidence of post- Mini-sling complications., Competing Interests: Declaration of competing interest Authors have no relevant conflicts of interest to this article., (Copyright © 2023. Published by Elsevier B.V.)
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- 2023
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184. Anatomical heterogeneity of residual disease in chronic lymphocytic leukemia treated with ibrutinib.
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Condoluci A, Milan L, Forestieri G, Terzi di Bergamo L, Spina V, Bruscaggin A, Deambrogi C, Moia R, Deodato M, Fahrni G, Mattarucchi R, Merli M, Gerber B, Stussi G, Passamonti F, Gregor M, Tedeschi A, Gaidano G, Rossi D, and Ceriani L
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- Humans, Neoplasm, Residual, Leukemia, Lymphocytic, Chronic, B-Cell drug therapy
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- 2022
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185. Ibrutinib dose intensity in high-risk chronic lymphocytic leukemia.
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Forestieri G, Terzi di Bergamo L, Deodato M, Frustaci AM, Moia R, Deambrogi C, Rasi S, Autore F, Merli M, Mattarucchi R, Fahrni G, Scarfo' L, Gussetti D, Bulian P, Zanatta A, Spina V, Bruscaggin A, Pini K, Piffaretti D, Pirosa MC, Salehi M, Marques de Almeida J, Passweg J, Cavalli F, Zucca E, Gerber B, Stussi G, Gattei V, Ghia P, Gregor M, Passamonti F, Laurenti L, Gaidano G, Tedeschi A, Rossi D, and Condoluci A
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- Humans, Leukemia, Lymphocytic, Chronic, B-Cell drug therapy
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- 2022
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186. Oocyte Quality Assessment in Breast Cancer: Implications for Fertility Preservation.
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Fabiani C, Guarino A, Meneghini C, Licata E, Paciotti G, Miriello D, Schiavi MC, Spina V, Corno R, Gallo M, and Rago R
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Background: The aim of this study was to evaluate the effects of breast cancer on the ovarian response and on oocyte quality following controlled ovarian hyperstimulation (COH)., Methods: This retrospective case-control study evaluated the effects of breast cancer on the ovarian response and on the oocyte quality. Oncological patients with breast cancer undergoing controlled ovarian stimulation cycles for fertility preservation, and age- and date-matched controls undergoing COH for in vitro fertilization (IVF) for male or tubal factor infertility were included in the study. Two hundred and ninety-four women were enrolled: 105 affected by breast cancer and 189 healthy women in the control group. Both groups were comparable in terms of age, BMI, and AMH value. Maximal estradiol levels on the triggering day, duration of stimulation, total amount of gonadotropins administered, number of oocytes retrieved, rate of metaphase 2 oocyte production, and numbers of immature and dysmorphic oocytes were analyzed., Results: Considering factors influencing the oocyte quality, such as age, BMI, AMH, duration of stimulation, E2 level on the triggering day, total FSH cumulative dose, stage, histotype, BRCA status, and hormone receptors, the univariate and multivariate analyses identified breast cancer as a risk factor for the presence of dysmorphic oocytes., Conclusions: The diagnosis of breast cancer does not seem to be associated with the impairment of the ovarian reserve, but is linked to a worsening oocyte quality.
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- 2022
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187. Is hypnotic assessment relevant to neurology?
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Fontanelli L, Spina V, Chisari C, Siciliano G, and Santarcangelo EL
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- Cognition, Humans, Hypnotics and Sedatives, Quality of Life, Hypnosis, Neurology
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Studies conducted in healthy subjects have clearly shown that different hypnotic susceptibility, which is measured by scales, is associated with different functional equivalence between imagery and perception/action (FE), cortical excitability, and information processing. Of note, physiological differences among individuals with high (highs), medium (mediums), and low hypnotizability scores (lows) have been observed in the ordinary state of consciousness, thus independently from the induction of the hypnotic state, and in the absence of specific suggestions. The potential role of hypnotic assessment and its relevance to neurological diseases have not been fully explored. While current knowledge and therapies allow a better survival rate, there is a constant need to optimize rehabilitation treatments and quality of life. The aim of this paper is to provide an overview of hypnotizability-related features and, specifically, to discuss the hypothesis that the stronger FE, the different mode of information processing, and the greater proneness to control pain and the activity of the immune system observed in individuals with medium-to-high hypnotizability scores have potential applications to neurology. Current evidence of the outcome of treatments based on hypnotic induction and suggestions administration is not consistent, mainly owing to the small sample size in clinical trials and inadequate control groups. We propose that hypnotic assessment may be feasible in clinical routine and give additional cues into the treatment and rehabilitation of neurological diseases., (© 2022. The Author(s).)
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- 2022
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188. Post-traumatic entrapment of the median nerve in the ulno-humeral joint: Diagnosis, treatment and literature review.
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Montanari S, Sartore R, Spina V, and Adani R
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- Adolescent, Child, Humans, Male, Median Nerve diagnostic imaging, Median Nerve surgery, Carpal Tunnel Syndrome, Elbow Joint diagnostic imaging, Elbow Joint surgery, Joint Dislocations surgery, Elbow Injuries
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Background: The incidence of median nerve injuries in pediatric elbow dislocations is approximately 3% and avulsion of the open medial epicondylar epiphysis in the pediatric population is one predisposing factor that may explain this age predilection. These lesions can be difficult to diagnose in the acute phase because symptoms tend to be mild or delayed, consequently their management can be challenging and functional outcome poorer., Methods: We present the case of an unrecognized median nerve entrapment in a 16-year-old boy with posterior dislocation of the elbow and a medial epicondyle fracture, treated initially with close reduction and open stabilization with a cannulated screw. Assessment is supported by a review of similar reported cases available in literature., Results: We discuss the diagnostic approach and the surgical options that can be used for this type of injury., Conclusions: High clinical suspicion of entrapment is imperative in presence of signs of damage to the median nerve in the pediatric patient immediately after the reduction of an elbow dislocation. If diagnosis of entrapment is made the therapeutic choice between neurolysis and nerve graft depends on the lesion severity. In the presence of a Fourrier's type 4 lesion, neurolysis should be avoided, while nerve resection and grafting are recommended., Competing Interests: Declaration of competing interest None., (Copyright © 2021 The Japanese Orthopaedic Association. Published by Elsevier B.V. All rights reserved.)
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- 2022
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189. Genetic and phenotypic attributes of splenic marginal zone lymphoma.
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Bonfiglio F, Bruscaggin A, Guidetti F, Terzi di Bergamo L, Faderl M, Spina V, Condoluci A, Bonomini L, Forestieri G, Koch R, Piffaretti D, Pini K, Pirosa MC, Cittone MG, Arribas A, Lucioni M, Ghilardi G, Wu W, Arcaini L, Baptista MJ, Bastidas G, Bea S, Boldorini R, Broccoli A, Buehler MM, Canzonieri V, Cascione L, Ceriani L, Cogliatti S, Corradini P, Derenzini E, Devizzi L, Dietrich S, Elia AR, Facchetti F, Gaidano G, Garcia JF, Gerber B, Ghia P, Gomes da Silva M, Gritti G, Guidetti A, Hitz F, Inghirami G, Ladetto M, Lopez-Guillermo A, Lucchini E, Maiorana A, Marasca R, Matutes E, Meignin V, Merli M, Moccia A, Mollejo M, Montalban C, Novak U, Oscier DG, Passamonti F, Piazza F, Pizzolitto S, Rambaldi A, Sabattini E, Salles G, Santambrogio E, Scarfò L, Stathis A, Stüssi G, Geyer JT, Tapia G, Tarella C, Thieblemont C, Tousseyn T, Tucci A, Vanini G, Visco C, Vitolo U, Walewska R, Zaja F, Zenz T, Zinzani PL, Khiabanian H, Calcinotto A, Bertoni F, Bhagat G, Campo E, De Leval L, Dirnhofer S, Pileri SA, Piris MA, Traverse-Glehen A, Tzankov A, Paulli M, Ponzoni M, Mazzucchelli L, Cavalli F, Zucca E, and Rossi D
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- Aged, Animals, Female, Humans, Male, Mice, Middle Aged, Chromosome Aberrations, Immunophenotyping, Multigene Family, Mutation, Spleen pathology, Transcriptome, Tumor Microenvironment, Lymphoma, B-Cell, Marginal Zone diagnosis, Lymphoma, B-Cell, Marginal Zone genetics, Splenic Neoplasms diagnosis, Splenic Neoplasms genetics
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Splenic marginal zone B-cell lymphoma (SMZL) is a heterogeneous clinico-biological entity. The clinical course is variable, multiple genes are mutated with no unifying mechanism, and essential regulatory pathways and surrounding microenvironments are diverse. We sought to clarify the heterogeneity of SMZL by resolving different subgroups and their underlying genomic abnormalities, pathway signatures, and microenvironment compositions to uncover biomarkers and therapeutic vulnerabilities. We studied 303 SMZL spleen samples collected through the IELSG46 multicenter international study (NCT02945319) by using a multiplatform approach. We carried out genetic and phenotypic analyses, defined self-organized signatures, validated the findings in independent primary tumor metadata and in genetically modified mouse models, and determined correlations with outcome data. We identified 2 prominent genetic clusters in SMZL, termed NNK (58% of cases, harboring NF-κB, NOTCH, and KLF2 modules) and DMT (32% of cases, with DNA-damage response, MAPK, and TLR modules). Genetic aberrations in multiple genes as well as cytogenetic and immunogenetic features distinguished NNK- from DMT-SMZLs. These genetic clusters not only have distinct underpinning biology, as judged by differences in gene-expression signatures, but also different outcomes, with inferior survival in NNK-SMZLs. Digital cytometry and in situ profiling segregated 2 basic types of SMZL immune microenvironments termed immune-suppressive SMZL (50% of cases, associated with inflammatory cells and immune checkpoint activation) and immune-silent SMZL (50% of cases, associated with an immune-excluded phenotype) with distinct mutational and clinical connotations. In summary, we propose a nosology of SMZL that can implement its classification and also aid in the development of rationally targeted treatments., (© 2022 by The American Society of Hematology.)
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- 2022
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190. Competing endogenous RNA network mediated by circ_3205 in SARS-CoV-2 infected cells.
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Barbagallo D, Palermo CI, Barbagallo C, Battaglia R, Caponnetto A, Spina V, Ragusa M, Di Pietro C, Scalia G, and Purrello M
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- Computational Biology, Gene Expression Regulation, Viral, Gene Regulatory Networks, Humans, Large-Conductance Calcium-Activated Potassium Channel beta Subunits genetics, MicroRNAs genetics, MicroRNAs metabolism, Nasopharynx virology, Nerve Tissue Proteins genetics, Protein Interaction Mapping, Protein Kinase C-epsilon genetics, Reproducibility of Results, COVID-19 genetics, COVID-19 metabolism, RNA, Circular genetics, RNA, Viral, SARS-CoV-2 genetics
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Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a new member of the Betacoronaviridae family, responsible for the recent pandemic outbreak of COVID-19. To start exploring the molecular events that follow host cell infection, we queried VirusCircBase and identified a circular RNA (circRNA) predicted to be synthesized by SARS-CoV-2, circ_3205, which we used to probe: (i) a training cohort comprised of two pools of cells from three nasopharyngeal swabs of SARS-CoV-2 infected (positive) or uninfected (negative, UCs) individuals; (ii) a validation cohort made up of 12 positive and 3 negative samples. The expression of circRNAs, miRNAs and miRNA targets was assayed through real-time PCR. CircRNA-miRNA interactions were predicted by TarpMiR, Analysis of Common Targets for circular RNAs (ACT), and STarMir tools. Enrichment of the biological processes and the list of predicted miRNA targets were retrieved from DIANA miRPath v3.0. Our results showed that the predicted SARS-CoV-2 circ_3205 was expressed only in positive samples and its amount positively correlated with that of SARS-CoV-2 Spike (S) mRNA and the viral load (r values = 0.80952 and 0.84867, Spearman's correlation test, respectively). Human (hsa) miR-298 was predicted to interact with circ_3205 by all three predictive tools. KCNMB4 and PRKCE were predicted as hsa-miR-298 targets. Interestingly, the function of both is correlated with blood coagulation and immune response. KCNMB4 and PRKCE mRNAs were upregulated in positive samples as compared to UCs (6 and 8.1-fold, p values = 0.049 and 0.02, Student's t test, respectively) and their expression positively correlated with that of circ_3205 (r values = 0.6 and 0.25, Spearman's correlation test, respectively). We propose that our results convincingly suggest that circ_3205 is a circRNA synthesized by SARS-CoV-2 upon host cell infection and that it may behave as a competitive endogenous RNA (ceRNA), sponging hsa-miR-298 and contributing to the upregulation of KCNMB4 and PRKCE mRNAs., (© 2022. The Author(s).)
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- 2022
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191. Female fertility preservation: Impact of cancer on ovarian function and oocyte quality.
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Fabiani C, Ferrante MG, Meneghini C, Licata E, Paciotti G, Gallo M, Schiavi M, Spina V, Guarino A, Caserta D, and Rago R
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- Chorionic Gonadotropin, Female, Fertilization in Vitro, Humans, Male, Oocyte Retrieval, Oocytes, Ovulation Induction, Prospective Studies, Fertility Preservation, Infertility, Female etiology, Neoplasms
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Objective: To evaluate the influence of cancer on ovarian response and oocyte quality in controlled ovarian hyperstimulation (COH)., Methods: This prospective study conducted at the Physiopathology of Reproduction and Andrology Unit of Sandro Pertini Hospital enrolled 82 cancer patients undergoing controlled ovarian stimulation (COH) cycles for fertility preservation, and age- and date-matched controls undergoing COH for in vitro fertilization for male-factor infertility from June 2016 to November 2019. The interventions performed were COH, oocyte retrieval, and quality evaluation. Main outcome measures were maximal estradiol levels on the day of human chorionic gonadotropin administration, duration of stimulation, total amount of gonadotropins administered, number of oocytes retrieved, and rates of metaphase 2 oocytes and abnormal oocytes. All data were analyzed using the Statistical Package for the Social Sciences (IBM Corp., Armonk, NY, USA) 22.0., Results: Intergroup comparisons (82 cancer patients and 180 patients in control group) showed a significant difference in ovarian response, especially for a significant higher number of abnormal oocytes in cancer patients (P < 0.0001). Regression analysis to assess the influence of the neoplastic process, regardless of the type, on ovarian response showed an effect on the main outcome measured due to cancer itself., Conclusion: Cancer influences the ovarian response, particularly the oocyte quality, during COH performed for fertility preservation., (© 2021 International Federation of Gynecology and Obstetrics.)
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- 2022
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192. Circulating tumor DNA for comprehensive noninvasive monitoring of lymphoma treated with ibrutinib plus nivolumab.
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Bruscaggin A, di Bergamo LT, Spina V, Hodkinson B, Forestieri G, Bonfiglio F, Condoluci A, Wu W, Pirosa MC, Faderl MR, Koch R, Schaffer M, Alvarez JD, Fourneau N, Gerber B, Stussi G, Zucca E, Balasubramanian S, and Rossi D
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- Adenine analogs & derivatives, Humans, Nivolumab therapeutic use, Piperidines, Pyrimidines, Circulating Tumor DNA genetics, Lymphoma, Large B-Cell, Diffuse
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To advance the use of circulating tumor DNA (ctDNA) applications, their broad clinical validity must be tested in different treatment settings, including targeted therapies. Using the prespecified longitudinal systematic collection of plasma samples in the phase 1/2a LYM1002 trial (registered on www.clinicaltrials.gov as NCT02329847), we tested the clinical validity of ctDNA for baseline mutation profiling, residual tumor load quantification, and acquisition of resistance mutations in patients with lymphoma treated with ibrutinib+nivolumab. Inclusion criterion for this ancillary biological study was the availability of blood collected at baseline and cycle 3, day 1. Overall, 172 ctDNA samples from 67 patients were analyzed by the LyV4.0 ctDNA Cancer Personalized Profiling Deep Sequencing Assay. Among baseline variants in ctDNA, only TP53 mutations (detected in 25.4% of patients) were associated with shorter progression-free survival; clones harboring baseline TP53 mutations did not disappear during treatment. Molecular response, defined as a >2-log reduction in ctDNA levels after 2 cycles of therapy (28 days), was achieved in 28.6% of patients with relapsed diffuse large B-cell lymphoma who had ≥1 baseline variant and was associated with best response and improved progression-free survival. Clonal evolution occurred frequently during treatment, and 10.3% new mutations were identified after 2 treatment cycles in nonresponders. PLCG2 was the topmost among genes that acquired new mutations. No patients acquired the C481S BTK mutation implicated in resistance to ibrutinib in CLL. Collectively, our results provide the proof of concept that ctDNA is useful for noninvasive monitoring of lymphoma treated with targeted agents in the clinical trial setting., (© 2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.)
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- 2021
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193. Robot-Assisted Training for Upper Limb in Stroke (ROBOTAS): An Observational, Multicenter Study to Identify Determinants of Efficacy.
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Calabrò RS, Morone G, Naro A, Gandolfi M, Liotti V, D'aurizio C, Straudi S, Focacci A, Pournajaf S, Aprile I, Filoni S, Zanetti C, Leo MR, Tedesco L, Spina V, Chisari C, Taveggia G, Mazzoleni S, Smania N, Paolucci S, Franceschini M, and Bonaiuti D
- Abstract
Background: The loss of arm function is a common and disabling outcome after stroke. Robot-assisted upper limb (UL) training may improve outcomes. The aim of this study was to explore the effect of robot-assisted training using end-effector and exoskeleton robots on UL function following a stroke in real-life clinical practice., Methods: A total of 105 patients affected by a first-ever supratentorial stroke were enrolled in 18 neurorehabilitation centers and treated with electromechanically assisted arm training as an add-on to conventional therapy. Both interventions provided either an exoskeleton or an end-effector device (as per clinical practice) and consisted of 20 sessions (3/5 times per week; 6-8 weeks). Patients were assessed by validated UL scales at baseline (T0), post-treatment (T1), and at three-month follow-up (T2). The primary outcome was the Fugl-Meyer Assessment for the upper extremity (FMA-UE)., Results: FMA-UE improved at T1 by 6 points on average in the end-effector group and 11 points on average in the exoskeleton group ( p < 0.0001). Exoskeletons were more effective in the subacute phase, whereas the end-effectors were more effective in the chronic phase ( p < 0.0001)., Conclusions: robot-assisted training might help improve UL function in stroke patients as an add-on treatment in both subacute and chronic stages. Pragmatic and highmethodological studies are needed to confirm the showed effectiveness of the exoskeleton and end-effector devices.
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- 2021
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194. Connectivity Measures Differentiate Cortical and Subcortical Sub-Acute Ischemic Stroke Patients.
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Fanciullacci C, Panarese A, Spina V, Lassi M, Mazzoni A, Artoni F, Micera S, and Chisari C
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Brain lesions caused by cerebral ischemia lead to network disturbances in both hemispheres, causing a subsequent reorganization of functional connectivity both locally and remotely with respect to the injury. Quantitative electroencephalography (qEEG) methods have long been used for exploring brain electrical activity and functional connectivity modifications after stroke. However, results obtained so far are not univocal. Here, we used basic and advanced EEG methods to characterize how brain activity and functional connectivity change after stroke. Thirty-three unilateral post stroke patients in the sub-acute phase and ten neurologically intact age-matched right-handed subjects were enrolled. Patients were subdivided into two groups based on lesion location: cortico-subcortical ( CS , n = 18) and subcortical ( S , n = 15), respectively. Stroke patients were evaluated in the period ranging from 45 days since the acute event (T0) up to 3 months after stroke (T1) with both neurophysiological (resting state EEG) and clinical assessment (Barthel Index, BI) measures, while healthy subjects were evaluated once. Brain power at T0 was similar between the two groups of patients in all frequency bands considered (δ, θ, α, and β). However, evolution of θ-band power over time was different, with a normalization only in the CS group. Instead, average connectivity and specific network measures ( Integration , Segregation , and Small-worldness ) in the β-band at T0 were significantly different between the two groups. The connectivity and network measures at T0 also appear to have a predictive role in functional recovery (BI T1-T0), again group-dependent. The results obtained in this study showed that connectivity measures and correlations between EEG features and recovery depend on lesion location. These data, if confirmed in further studies, on the one hand could explain the heterogeneity of results so far observed in previous studies, on the other hand they could be used by researchers as biomarkers predicting spontaneous recovery, to select homogenous groups of patients for the inclusion in clinical trials., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Fanciullacci, Panarese, Spina, Lassi, Mazzoni, Artoni, Micera and Chisari.)
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- 2021
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195. Osteoid Osteoma of the Atlas in a Boy: Clinical and Imaging Features-A Case Report and Review of the Literature.
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Valluzzi A, Donatiello S, Gallo G, Cellini M, Maiorana A, Spina V, and Pavesi G
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- Child, Humans, Magnetic Resonance Imaging, Male, Tomography, X-Ray Computed, Torticollis etiology, Cervical Atlas diagnostic imaging, Cervical Atlas pathology, Cervical Atlas surgery, Osteoma, Osteoid complications, Osteoma, Osteoid diagnostic imaging, Osteoma, Osteoid pathology, Osteoma, Osteoid surgery, Spinal Neoplasms complications, Spinal Neoplasms diagnostic imaging, Spinal Neoplasms pathology, Spinal Neoplasms surgery
- Abstract
Osteoid osteoma is a benign osteoblastic tumor, quite uncommon in the spine. We report a case of an osteoid osteoma involving the atlas in a 6-year-old boy, who presented with suboccipital pain and torticollis. Initial radiological findings were ambiguous as magnetic resonance imaging showed mainly edema of upper cervical soft tissues. The subsequent computed tomography depicted a lesion of left lamina of C1. As conservative treatment failed, the lesion was surgically resected and the patient became pain free. To our knowledge, this is the first case of osteoid osteoma involving the atlas associated with abnormal soft tissue reaction reported in literature., Competing Interests: None., (Thieme. All rights reserved.)
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- 2021
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196. Liver steatosis is highly prevalent and is associated with metabolic risk factors and liver fibrosis in adult patients with type 1 Gaucher disease.
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Nascimbeni F, Lugari S, Cassinerio E, Motta I, Cavicchioli A, Dalla Salda A, Bursi S, Donatiello S, Spina V, Cappellini MD, Andreone P, and Carubbi F
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- Adult, Humans, Liver Cirrhosis epidemiology, Risk Factors, Elasticity Imaging Techniques, Fatty Liver epidemiology, Gaucher Disease complications, Gaucher Disease epidemiology, Non-alcoholic Fatty Liver Disease complications, Non-alcoholic Fatty Liver Disease epidemiology
- Abstract
Background and Aims: Gaucher disease (GD) is associated with peculiar metabolic abnormalities (ie hypermetabolic state, peripheral insulin resistance, dyslipidaemia), partially reverted by enzyme replacement therapy (ERT) at the expense of weight gain. Such metabolic alterations together with an unhealthy lifestyle acquired by an ageing GD population may favour the development of liver steatosis. We aimed at evaluating the prevalence of significant liver steatosis and at identifying the factors associated with liver steatosis in a cohort of patients with type 1 GD., Methods: Twenty adult type 1 GD patients from an Italian academic referral centre were prospectively submitted to vibration-controlled transient elastography (Fibroscan®) with controlled attenuation parameter (CAP); significant steatosis was defined as CAP values ≥250 dB/min., Results: Median CAP values were 234 [165-358] dB/min and 8 patients (40%) had significant steatosis. Significant steatosis was associated with indices of adiposity (weight, BMI and waist circumference), high blood pressure, insulin resistance and metabolic syndrome. GD-related variables and dose and duration of ERT were not associated with significant steatosis. In the subgroup of 16 patients on stable ERT for at least 24 months, CAP resulted significantly and positively associated with liver stiffness (rho 0.559, P = .024)., Conclusions: Significant steatosis is highly prevalent in adult type 1 GD patients and is strongly associated with a worse metabolic profile, featuring metabolic dysfunction-associated fatty liver disease (MAFLD). MAFLD may determine liver fibrosis progression in GD patients on stable ERT and may be a risk factor for long-term liver-related complications., (© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2020
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197. Frequency and clinical relevance of coding and noncoding NOTCH1 mutations in early stage Binet A chronic lymphocytic leukemia patients.
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Lionetti M, Barbieri M, Favasuli V, Taiana E, Fabris S, Favoino C, Ciceri G, Matis S, Colombo M, Massara R, Reda G, Gentile M, Spina V, Rossi D, Baldini L, Gaidano G, Fais F, Ferrarini M, Morabito F, Cutrona G, and Neri A
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- Humans, Neoplasm Staging, Prognosis, Prospective Studies, Survival Rate, Leukemia, Lymphocytic, Chronic, B-Cell genetics, Leukemia, Lymphocytic, Chronic, B-Cell pathology, Mutation, Receptor, Notch1 genetics, Untranslated Regions genetics
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- 2020
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198. Love in the Time of COVID-19: Sexual Function and Quality of Life Analysis During the Social Distancing Measures in a Group of Italian Reproductive-Age Women.
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Schiavi MC, Spina V, Zullo MA, Colagiovanni V, Luffarelli P, Rago R, and Palazzetti P
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- Adult, COVID-19, Coronavirus Infections epidemiology, Female, Humans, Italy epidemiology, Male, Middle Aged, Physical Distancing, Pneumonia, Viral epidemiology, SARS-CoV-2, Sexual Partners, Surveys and Questionnaires, Betacoronavirus, Coronavirus Infections prevention & control, Pandemics prevention & control, Pneumonia, Viral prevention & control, Quality of Life, Sexual Behavior psychology, Stress, Psychological
- Abstract
Background: The beginning of 2020 was characterized by the COVID-19 pandemic. The world governments have adopted restrictive measures to reduce the spread of infection. These measures could affect the sexual function and quality of life of women living with their partner., Aim: The aim is to assess the impact of the social distancing measures caused by the COVID-19 pandemic on sexual function and quality of life of noninfected reproductive-age women, living with their sexual partner., Methods: Observational analysis on sexually active women, living with their partner, and without COVID-19 infection was performed. The population previously answered FSFI, FSDS, and SF-36 questionnaires. 4 weeks after the introduction of the restrictive measures, these women were invited to complete the same questionnaires by e-mail for an evaluation during the COVID-19 outbreak., Main Outcome Measures: The primary endpoint was the assessment of the women's sex function change during the social restriction period, by analyzing the FSFI and FSDS questionnaires. The secondary endpoint was the evaluation of the impact on the quality of life calculated by the SF-36 questionnaire., Results: 89 patients were considered. The median age was 39 (28-50) years. Mean sexual intercourses/month decreased from 6.3 ± 1.9 to 2.3 ± 1.8, mean difference: -3.9 ± 1.2. FSFI decreased significantly (29.2 ± 4.2 vs 19.2 ± 3.3, mean difference: -9.7 ± 2.6) and FSDS increased significantly (9.3 ± 5.5 vs 20.1 ± 5.2, mean difference: 10.8 ± 3.4). The SF-36 showed a significant change from 82.2 ± 10.2 to 64.2 ± 11.8 4 weeks after the introduction of the restrictive measures; mean difference: -17.8 ± 6.7. The univariable analysis identified working outside the home, university educational level, and parity ≥1 as predictive factors of lower FSFI. In multivariable analysis, working outside the home and combination of working outside the home + university educational level + parity ≥1 were the independent factors of a lower FSFI., Clinical Implication: The negative impact of the COVID-19 epidemic period on sexual function and quality of life in women shows how acute stress might affect the psychological state. Thus, psychological or sexual support could be useful., Strengths and Limitations: To our knowledge, this study is the first that analyzes the change in sexual activity in women during the COVID-19 outbreak period. The limitations were the low number of the analyzed participants, psychological tests were not included, and no data were collected on masturbation, self-heroism, solitary, and nonpenetrative sex., Conclusion: The COVID-19 epidemic and the restrictive social distancing measures have negatively influenced the sexual function and quality of life in not-infected reproductive-age women who live with their sexual partners. Schiavi MC, Spina V, Zullo MA, et al. Love in the Time of COVID-19: Sexual Function and Quality of Life Analysis During the Social Distancing Measures in a Group of Italian Reproductive-Age Women. J Sex Med 2020;17:1407-1413., (Copyright © 2020 International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.)
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- 2020
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199. KMT2D mutations and TP53 disruptions are poor prognostic biomarkers in mantle cell lymphoma receiving high-dose therapy: a FIL study.
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Ferrero S, Rossi D, Rinaldi A, Bruscaggin A, Spina V, Eskelund CW, Evangelista A, Moia R, Kwee I, Dahl C, Di Rocco A, Stefoni V, Diop F, Favini C, Ghione P, Mahmoud AM, Schipani M, Kolstad A, Barbero D, Novero D, Paulli M, Zamò A, Jerkeman M, da Silva MG, Santoro A, Molinari A, Ferreri A, Grønbæk K, Piccin A, Cortelazzo S, Bertoni F, Ladetto M, and Gaidano G
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- Adult, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Humans, Mutation, Prognosis, Prospective Studies, Transplantation, Autologous, DNA-Binding Proteins genetics, Hematopoietic Stem Cell Transplantation, Lymphoma, Mantle-Cell diagnosis, Lymphoma, Mantle-Cell drug therapy, Lymphoma, Mantle-Cell genetics, Neoplasm Proteins genetics, Tumor Suppressor Protein p53 genetics
- Abstract
In recent years, the outcome of mantle cell lymphoma (MCL) has improved, especially in younger patients, receiving cytarabine-containing chemoimmunotherapy and autologous stem cell transplantation. Nevertheless, a proportion of MCL patients still experience early failure. To identify biomarkers anticipating failure of intensive chemotherapy in MCL, we performed target resequencing and DNA profiling of purified tumor samples collected from patients enrolled in the prospective FIL-MCL0208 phase 3 trial (high-dose chemoimmunotherapy followed by autologous transplantation and randomized lenalidomide maintenance). Mutations of KMT2D and disruption of TP53 by deletion or mutation associated with an increased risk of progression and death, both in univariate and multivariate analysis. By adding KMT2D mutations and TP53 disruption to the MIPI-c backbone, we derived a new prognostic index, the "MIPI-genetic" ("MIPI- g"). The "MIPI-g" improved the model discrimination ability compared to the MIPI-c alone, defining three risk groups: i) low-risk patients (4-year progression free survival and overall survival of 72.0% and 94.5%); ii) inter-mediate-risk patients (4-year progression free survival and overall survival of 42.2% and 65.8%) and iii) high-risk patients (4-year progression free survival and overall survival of 11.5% and 44.9%). Our results: i) confirm that TP53 disruption identifies a high-risk population characterized by poor sensitivity to conventional or intensified chemotherapy; ii) provide the pivotal evidence that patients harboring KMT2D mutations share the same poor outcome as patients harboring TP53 disruption; and iii) allow to develop a tool for the identification of high-risk MCL patients for whom novel therapeutic strategies need to be investigated. ( Trial registered at clinicaltrials.gov identifier: NCT02354313 )., (Copyright© 2020 Ferrata Storti Foundation.)
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- 2020
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200. International prognostic score for asymptomatic early-stage chronic lymphocytic leukemia.
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Condoluci A, Terzi di Bergamo L, Langerbeins P, Hoechstetter MA, Herling CD, De Paoli L, Delgado J, Rabe KG, Gentile M, Doubek M, Mauro FR, Chiodin G, Mattsson M, Bahlo J, Cutrona G, Kotaskova J, Deambrogi C, Smedby KE, Spina V, Bruscaggin A, Wu W, Moia R, Bianchi E, Gerber B, Zucca E, Gillessen S, Ghielmini M, Cavalli F, Stussi G, Hess MA, Baumann TS, Neri A, Ferrarini M, Rosenquist R, Forconi F, Foà R, Pospisilova S, Morabito F, Stilgenbauer S, Döhner H, Parikh SA, Wierda WG, Montserrat E, Gaidano G, Hallek M, and Rossi D
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- Aged, Combined Modality Therapy, Disease Progression, Female, Follow-Up Studies, Humans, Leukemia, Lymphocytic, Chronic, B-Cell genetics, Leukemia, Lymphocytic, Chronic, B-Cell therapy, Male, Prognosis, Retrospective Studies, Survival Rate, Biomarkers, Tumor genetics, Clinical Trials as Topic statistics & numerical data, Leukemia, Lymphocytic, Chronic, B-Cell pathology, Mutation, Nomograms
- Abstract
Most patients with chronic lymphocytic leukemia (CLL) are diagnosed with early-stage disease and managed with active surveillance. The individual course of patients with early-stage CLL is heterogeneous, and their probability of needing treatment is hardly anticipated at diagnosis. We aimed at developing an international prognostic score to predict time to first treatment (TTFT) in patients with CLL with early, asymptomatic disease (International Prognostic Score for Early-stage CLL [IPS-E]). Individual patient data from 11 international cohorts of patients with early-stage CLL (n = 4933) were analyzed to build and validate the prognostic score. Three covariates were consistently and independently correlated with TTFT: unmutated immunoglobulin heavy variable gene (IGHV), absolute lymphocyte count higher than 15 × 109/L, and presence of palpable lymph nodes. The IPS-E was the sum of the covariates (1 point each), and separated low-risk (score 0), intermediate-risk (score 1), and high-risk (score 2-3) patients showing a distinct TTFT. The score accuracy was validated in 9 cohorts staged by the Binet system and 1 cohort staged by the Rai system. The C-index was 0.74 in the training series and 0.70 in the aggregate of validation series. By meta-analysis of the training and validation cohorts, the 5-year cumulative risk for treatment start was 8.4%, 28.4%, and 61.2% among low-risk, intermediate-risk, and high-risk patients, respectively. The IPS-E is a simple and robust prognostic model that predicts the likelihood of treatment requirement in patients with early-stage CLL. The IPS-E can be useful in clinical management and in the design of early intervention clinical trials., (© 2020 by The American Society of Hematology.)
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- 2020
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