23 results on '"Erika Pace"'
Search Results
2. Imaging of pediatric abdominal soft tissue tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
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Abhay Srinivasan, Ashishkumar Parikh, Erika Pace, Ann Schechter, Elizabeth Tang, and Sabah Servaes
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Oncology ,Pediatrics, Perinatology and Child Health ,Hematology - Published
- 2023
3. European Society of Paediatric Radiology Artificial Intelligence taskforce: a new taskforce for the digital age
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Lene Bjerke Laborie, Jaishree Naidoo, Erika Pace, Pierluigi Ciet, Christine Eade, Matthias W. Wagner, Thierry A. G. M. Huisman, Susan C. Shelmerdine, Radiology & Nuclear Medicine, and Pediatrics
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Pediatrics, Perinatology and Child Health ,Radiology, Nuclear Medicine and imaging - Abstract
A new task force dedicated to artificial intelligence (AI) with respect to paediatric radiology was created in 2021 at the International Paediatric Radiology (IPR) meeting in Rome, Italy (a joint society meeting by the European Society of Pediatric Radiology [ESPR] and the Society for Pediatric Radiology [SPR]). The concept of a separate task force dedicated to AI was borne from an ESPR-led international survey of health care professionals’ opinions, expectations and concerns regarding AI integration within children’s imaging departments. In this survey, the majority (> 80%) of ESPR respondents supported the creation of a task force and helped define our key objectives. These include providing educational content about AI relevant for paediatric radiologists, brainstorming ideas for future projects and collaborating on AI-related studies with respect to collating data sets, de-identifying images and engaging in multi-case, multi-reader studies. This manuscript outlines the starting point of the ESPR AI task force and where we wish to go.
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- 2023
4. Respiratory-Triggered Flow-Independent Noncontrast Non–ECG-Gated MRV (REACT) Versus Contrast-Enhanced MRV for Central Venous Evaluation in Children and Young Adults: A Six-Reader Study
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Lisa H. Betz, Jonathan R. Dillman, Alexander J. Towbin, Christopher G. Anton, Govind B. Chavhan, Eric J. Crotty, Cara E. Morin, Erika Pace, Gayathri Sreedher, Bin Zhang, and Jean A. Tkach
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Radiology, Nuclear Medicine and imaging ,General Medicine - Published
- 2023
5. North American Biliary Stricture Management Strategies in Children After Liver Transplantation: A Multicenter Analysis From the Society of Pediatric Liver Transplantation (SPLIT) Registry
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Veronika Shabanova, Amy G. Feldman, John C. Bucuvalas, Nitika A. Gupta, Erika Pace, Vicky L. Ng, Pamela L. Valentino, Regino P. Gonzalez-Peralta, Kyle Soltys, Shikha S. Sundaram, Nada Yazigi, Tianhao Wang, Saeed Mohammad, and Tamir Miloh
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medicine.medical_specialty ,medicine.medical_treatment ,Subgroup analysis ,Constriction, Pathologic ,Liver transplantation ,Anastomosis ,Percutaneous transhepatic cholangiography ,Article ,medicine ,Operative report ,Humans ,Registries ,Child ,Retrospective Studies ,Cholangiopancreatography, Endoscopic Retrograde ,Transplantation ,Cholestasis ,Endoscopic retrograde cholangiopancreatography ,Hepatology ,medicine.diagnostic_test ,business.industry ,Liver Transplantation ,Surgery ,Hepatic artery thrombosis ,Treatment Outcome ,North America ,Outcomes research ,business - Abstract
Biliary strictures affect 4%−12% of pediatric liver transplantations. Biliary strictures can contribute to graft loss if left untreated; however, there remains no consensus on the best course of treatment. Study objectives included analyses of outcomes associated with biliary stricture management strategies via percutaneous transhepatic cholangiography (PTC), endoscopic retrograde cholangiopancreatography (ERCP), or surgery. We identified pediatric liver transplantation recipients (2011–2016) with biliary strictures from the Society of Pediatric Liver Transplantation (SPLIT) registry and retrieved imaging, procedural, and operative reports from individual centers. Subanalyses were performed to specifically evaluate PTC and ERCP for “optimal biliary outcome” (OBO), defined as graft survival with stricture resolution and without recurrence or surgery. A total of 113 children with a median follow-up of 3.9 years had strictures diagnosed 100 days (interquartile range, 30–290) after liver transplantation; 81% were isolated anastomotic strictures. Stricture resolution was achieved in 92% within 101 days, more frequently with isolated anastomotic strictures (96%). 20% of strictures recurred, more commonly in association with hepatic artery thrombosis (32%). Patient and graft survival at 1 and 3 years were 99% and 98% and 94% and 92%, respectively. In a subgroup analysis of 79 patients with extrahepatic strictures managed by PTC/ERCP, 59% achieved OBO following a median of 4 PTC, and 75% following a median of 3 ERCP (P < 0.001). Among patients with OBO, those with ERCP had longer time intervals between successive procedures (41, 47, 54, 62, 71 days) than for PTC (27, 31, 36, 41, 48 days; P < 0.001). Allograft salvage was successful across all interventions. Stricture resolution was achieved in 92%, with 20% risk of recurrence. Resolution without recurrence was highest in patients with isolated anastomotic strictures and without hepatic artery thrombosis.
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- 2022
6. Molecular Characterization of Circulating Tumor DNA in Pediatric Rhabdomyosarcoma: A Feasibility Study
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Olivia Ruhen, Nathalie S.M. Lak, Janine Stutterheim, Sara G. Danielli, Mathieu Chicard, Yasmine Iddir, Alexandra Saint-Charles, Virginia Di Paolo, Lucia Tombolan, Susanne A. Gatz, Ewa Aladowicz, Paula Proszek, Sabri Jamal, Reda Stankunaite, Deborah Hughes, Paul Carter, Elisa Izquierdo, Ajla Wasti, Julia C. Chisholm, Sally L. George, Erika Pace, Louis Chesler, Isabelle Aerts, Gaelle Pierron, Sakina Zaidi, Olivier Delattre, Didier Surdez, Anna Kelsey, Michael Hubank, Paolo Bonvini, Gianni Bisogno, Angela Di Giannatale, Gudrun Schleiermacher, Beat W. Schäfer, Godelieve A.M. Tytgat, and Janet Shipley
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Cancer Research ,Tumor ,Humans ,Child ,Mice ,Animals ,Feasibility Studies ,Prospective Studies ,Biomarkers, Tumor ,Mutation ,Circulating Tumor DNA ,Neoplasms ,Rhabdomyosarcoma, Embryonal ,Embryonal ,Oncology ,Rhabdomyosarcoma ,Biomarkers - Abstract
PURPOSE Rhabdomyosarcomas (RMS) are rare neoplasms affecting children and young adults. Efforts to improve patient survival have been undermined by a lack of suitable disease markers. Plasma circulating tumor DNA (ctDNA) has shown promise as a potential minimally invasive biomarker and monitoring tool in other cancers; however, it remains underexplored in RMS. We aimed to determine the feasibility of identifying and quantifying ctDNA in plasma as a marker of disease burden and/or treatment response using blood samples from RMS mouse models and patients. METHODS We established mouse models of RMS and applied quantitative polymerase chain reaction (PCR) and droplet digital PCR (ddPCR) to detect ctDNA within the mouse plasma. Potential driver mutations, copy-number alterations, and DNA breakpoints associated with PAX3/ 7-FOXO1 gene fusions were identified in the RMS samples collected at diagnosis. Patient-matched plasma samples collected from 28 patients with RMS before, during, and after treatment were analyzed for the presence of ctDNA via ddPCR, panel sequencing, and/or whole-exome sequencing. RESULTS Human tumor-derived DNA was detectable in plasma samples from mouse models of RMS and correlated with tumor burden. In patients, ctDNA was detected in 14/18 pretreatment plasma samples with ddPCR and 7/7 cases assessed by sequencing. Levels of ctDNA at diagnosis were significantly higher in patients with unfavorable tumor sites, positive nodal status, and metastasis. In patients with serial plasma samples (n = 18), fluctuations in ctDNA levels corresponded to treatment response. CONCLUSION Comprehensive ctDNA analysis combining high sensitivity and throughput can identify key molecular drivers in RMS models and patients, suggesting potential as a minimally invasive biomarker. Preclinical assessment of treatments using mouse models and further patient testing through prospective clinical trials are now warranted.
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- 2022
7. Imaging of pediatric pulmonary tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
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Paul G. Thacker, Ramesh S. Iyer, Erika Pace, Lisa J. States, and R. Paul Guillerman
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Oncology ,Pediatrics, Perinatology and Child Health ,Hematology - Abstract
Pediatric pulmonary malignancy can be primary or metastatic, with the latter being by far the more common. With a few exceptions, there are no well-established evidence-based guidelines for imaging pediatric pulmonary malignancies, although computed tomography (CT) is used in almost all cases. The aim of this article is to provide general imaging guidelines for pediatric pulmonary malignancies, including minimum standards for cross-sectional imaging techniques and specific imaging recommendations for select entities.
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- 2022
8. Imaging of pediatric extremity soft tissue tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
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Michael Richard Acord, Erika Pace, Alexander El‐Ali, Apeksha Chaturvedi, Ramesh S Iyer, Oscar M Navarro, Neeta Pandit‐Taskar, Ashishkumar K Parikh, Ann Schechter, Raja Shaikh, and M Beth McCarville
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Oncology ,Pediatrics, Perinatology and Child Health ,Hematology - Abstract
Pediatric soft tissue tumors of the extremity include rhabdomyosarcoma and nonrhabdomyosarcoma neoplasms. This manuscript provides consensus-based imaging recommendations for imaging evaluation at diagnosis, during treatment, and following completion of therapy for patients with a soft tissue tumor of the extremity.
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- 2022
9. Imaging of Pediatric Extragonadal Pelvic Soft Tissue Tumors: A COG Diagnostic Imaging Committee / SPR Oncology Committee White Paper
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Erika Pace, Tatum Johnson, Simon Kao, Ashishkumar Parikh, Jing Qi, Dhanashree Rajderkar, Janet R. Reid, Alexander Towbin, and Lisa States
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The most common pediatric extragonadal pelvic cancers include germ cell tumors, sacrococcygeal teratomas, and rhabdomyosarcomas (arising from the urinary bladder, prostate, paratesticular tissues, vagina, uterus, and perineum). This manuscript describes the radiological and nuclear medicine features of these entities and provides consensus-based recommendations for the assessment at diagnosis, during and after treatment.
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- 2022
10. Imaging of pediatric extragonadal pelvic soft tissue tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
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Erika Pace, Tatum S. Johnson, Simon C. Kao, Ashish K. Parikh, Jing Qi, Dhanashree A. Rajderkar, Janet R. Reid, Alexander J. Towbin, and Lisa J. States
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Oncology ,Pediatrics, Perinatology and Child Health ,Hematology - Abstract
The most common pediatric extragonadal pelvic cancers include germ cell tumors, sacrococcygeal teratomas, and rhabdomyosarcomas (arising from the urinary bladder, prostate, paratesticular tissues, vagina, uterus, and perineum). This paper describes the radiological and nuclear medicine features of these entities and provides consensus-based recommendations for the assessment at diagnosis, during, and after treatment.
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- 2022
11. Is it possible to achieve long-term survival in relapsed intracranial non-germinomatous germ cell tumours?
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Mohamed Magdy Ahmed, Stergios Zacharoulis, Istvan Bodi, Erika Pace, Henry Mandeville, Joanna Stone, Tony Elias, Bassel Zebian, and Fernando Carceller
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Oncology ,Brain Neoplasms ,Pediatrics, Perinatology and Child Health ,Humans ,Hematology ,Germinoma ,Neoplasms, Germ Cell and Embryonal - Published
- 2022
12. A Nationwide Evaluation of Bevacizumab-based Treatments in Paediatric Low-Grade Glioma in the UK: Safety. Efficacy, Visual Morbidity and Outcomes
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Katherine Green, Paraskevi Panagopoulou, Felice D’Arco, Patricia O’Hare, Richard Bowman, Bronwen Walters, Christine Dahl, Mette Jorgensen, Pritesh Patel, Olga Slater, Rehana Ahmed, Simon Bailey, Fernando Carceller, Rhiannon Collins, Elizabeth Corley, Martin English, Lisa Howells, Ahmed Kamal, John-Paul (JP) Kilday, Stephen Lowis, Blanche Lumb, Erika Pace, Susan Picton, Barry Pizer, Ayad Shafiq, Lena Uzunova, Harriet Wayman, Shaun Wilson, Darren Hargrave, and Enrico Opocher
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Cancer Research ,Oncology ,Neurology (clinical) - Abstract
Background Bevacizumab is increasingly used in children with pediatric low-grade glioma (PLGG) despite limited evidence. A nationwide UK service evaluation was conducted to provide larger cohort “real life” safety and efficacy data including functional visual outcomes. Methods Children receiving bevacizumab-based treatments (BBT) for PLGG (2009–2020) from 11 centers were included. Standardized neuro-radiological (RANO-LGG) and visual (logMAR visual acuity) criteria were used to assess clinical–radiological correlation, survival outcomes and multivariate prognostic analysis. Results Eighty-eight children with PLGG received BBT either as 3rd line with irinotecan (85%) or alongside 1st/2nd line chemotherapies (15%). Toxicity was limited and minimal. Partial response (PR, 40%), stable disease (SD, 49%), and progressive disease (PD, 11%) were seen during BBT. However, 65% progressed at 8 months (median) from BBT cessation, leading to a radiology-based 3 yr-progression-free survival (PFS) of 29%. Diencephalic syndrome (P = .03) was associated with adverse PFS. Pre-existing visual morbidity included unilateral (25%) or bilateral (11%) blindness. Improvement (29%) or stabilization (49%) of visual acuity was achieved, more often in patients’ best eyes. Vision deteriorated during BBT in 14 (22%), with 3-year visual-PFS of 53%; more often in patients’ worst eyes. A superior visual outcome (P = .023) was seen in neurofibromatosis type 1-associated optic pathway glioma (OPG). Concordance between visual and radiological responses was 36%; optimized to 48% using only best eye responses. Conclusions BBTs provide effective short-term PLGG control and delay further progression, with a better sustained visual (best > worst eye) than radiological response. Further research could optimize the role of BBT toward a potentially sight-saving strategy in OPG.
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- 2022
13. To the editor: Is it possible to achieve long-term survival in relapsed Intracranial Non-Germinomatous Germ Cell Tumours?
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Mohamed Ahmed, Stergios Zacharoulis, Istvan Bodi, Erika Pace, Henry Mandeville, Joanna Stone, Tony Elias, Bassel Zebian, and Fernando Carceller
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- 2022
14. Diffusion-weighted MRI in Advanced Epithelial Ovarian Cancer: Apparent Diffusion Coefficient as a Response Marker
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Susan Freeman, Jessica M. Winfield, Rebecca A. Quest, Susana Banerjee, Jennifer C. Wakefield, Hani Gabra, Nandita M. deSouza, Liam McKnight, Kerryn Lutchman-Singh, David Dolling, Marcia Hall, Emma Hall, David J. Collins, Andrew N. Priest, N. Jane Taylor, Erika Pace, and James D. Brenton
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medicine.medical_specialty ,Urology ,Carcinoma, Ovarian Epithelial ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Interquartile range ,Multicenter trial ,Biomarkers, Tumor ,Humans ,Medicine ,Radiology, Nuclear Medicine and imaging ,Prospective Studies ,Prospective cohort study ,Survival rate ,Aged ,Neoplasm Staging ,business.industry ,Hazard ratio ,Middle Aged ,Debulking ,Combined Modality Therapy ,Confidence interval ,Survival Rate ,Diffusion Magnetic Resonance Imaging ,030220 oncology & carcinogenesis ,Cohort ,Female ,Neoplasm Recurrence, Local ,business - Abstract
Background Treatment of advanced epithelial ovarian cancer results in a relapse rate of 75%. Early markers of response would enable optimization of management and improved outcome in both primary and recurrent disease. Purpose To assess the apparent diffusion coefficient (ADC), derived from diffusion-weighted MRI, as an indicator of response, progression-free survival (PFS), and overall survival. Materials and Methods This prospective multicenter trial (from 2012-2016) recruited participants with stage III or IV ovarian, primary peritoneal, or fallopian tube cancer (newly diagnosed, cohort one; relapsed, cohort two) scheduled for platinum-based chemotherapy, with interval debulking surgery in cohort one. Cohort one underwent two baseline MRI examinations separated by 0-7 days to assess ADC repeatability; an additional MRI was performed after three treatment cycles. Cohort two underwent imaging at baseline and after one and three treatment cycles. ADC changes in responders and nonresponders were compared (Wilcoxon rank sum tests). PFS and overall survival were assessed by using a multivariable Cox model. Results A total of 125 participants (median age, 63.3 years [interquartile range, 57.0-70.7 years]; 125 women; cohort one, n = 47; cohort two, n = 78) were included. Baseline ADC (range, 77-258 × 10-5mm2s-1) was repeatable (upper and lower 95% limits of agreement of 12 × 10-5mm2s-1 [95% confidence interval {CI}: 6 × 10-5mm2s-1 to 18 × 10-5mm2s-1] and -15 × 10-5mm2s-1 [95% CI: -21 × 10-5mm2s-1 to -9 × 10-5mm2s-1]). ADC increased in 47% of cohort two after one treatment cycle, and in 58% and 53% of cohorts one and two, respectively, after three cycles. Percentage change from baseline differed between responders and nonresponders after three cycles (16.6% vs 3.9%; P = .02 [biochemical response definition]; 19.0% vs 6.2%; P = .04 [radiologic definition]). ADC increase after one cycle was associated with longer PFS in cohort two (adjusted hazard ratio, 0.86; 95% CI: 0.75, 0.98; P = .03). ADC change was not indicative of overall survival for either cohort. Conclusion After three cycles of platinum-based chemotherapy, apparent diffusion coefficient (ADC) changes are indicative of response. After one treatment cycle, increased ADC is indicative of improved progression-free survival in relapsed disease. Published under a CC BY 4.0 license. Online supplemental material is available for this article.
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- 2019
15. LGG-09. A Nationwide Service Evaluation of Safety, Radiologic and Visual Outcome Refining Bevacizumab-based Treatments in Children with Progressive Low-Grade Glioma
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Katherine Green, Paraskevi Panagopoulou, Felice D’Arco, Patricia O'Hare, Richard Bowman, Bronwen Walters, Christine Dahl, Mette Jorgensen, Pritesh Patel, Olga Slater, Rehana Ahmed, Simon Bailey, Fernando Carceller, Rhiannon Collins, Elizabeth Corley, Martin English, James Hayden, Lisa Howells, Ahmed Kamal, John Paul Kilday, Stephen Lowis, Blanche Lumb, Thomas Micic, Dip Mitra, Erika Pace, Susan Picton, Barry Pizer, Ayad Shafiq, Lena Uzunova, Shaun Wilson, Harriet Wayman, Darren Hargrave, and Enrico Opocher
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Cancer Research ,Oncology ,Neurology (clinical) - Abstract
INTRODUCTION: Bevacizumab/Irinotecan is currently 3rd-line treatment in the UK for progressive Paediatric Low-Grade Glioma (PLGG) based on limited evidence. A nationwide service evaluation was conducted to review its safety and efficacy amongst a larger cohort. METHODS: Data from children with PLGG receiving Bevacizumab-based Treatments (BBT) from 11 UK Centres (2009-2020) were reviewed. Radiological and visual outcomes were based on standardized measurements. Clinical-radiological correlation was investigated. Time to progression from BBT stop, progression free-survival (PFS) curves and multivariate analysis of prognostic factors (p 0.05) were performed. RESULTS: 88 children with PLGG (88% OPG, 24% NF1) had BBT for radiological (43%), visual (20%) or combined (27%) progression, after 40 months (median) from diagnosis. Amongst OPG cases, visual acuity (VA) per eye (better/worse) before BBT was logMAR 0.0-0.3 (23/7) 0.3 - 1.0 (27/20), > 1.0 (14/18) and LP/NLP (8/27), with 19/8 children respectively blind (LP/NLP) in one or both eyes. Bevacizumab 10 mg/kg every 14 days (median 24 doses) was given as 3rd line+ with Irinotecan (85%) or alongside 1st/2nd line chemo (15%) leading to remarkable radiological (88%) and visual (74%) responses (stable or improved) within 3-6 months, with limited toxicity. 12% progressed on treatment, and 8% died unrelated to BBT. After initial response 65% progressed at a median of 8 months (4 - 23) after BBT, resulting in 3-year-all-causes-PFS of 16% and 3-yr-visual-PFS of 45% from start of BBT. Visual concordance with MRI was poor (36%) but increases (47%) when better-eye determines visual outcome. Lack of NF1 and diencephalic syndrome (DS) at presentation were independent negative prognostic factors for PFS. CONCLUSIONS: A remarkable but transient effect of BBT has been confirmed. Visual > radiological responses can be sustained after BBT. Variations in current BBT strategies justifies further research, including the potential upfront use alongside conventional first-line chemotherapy as sight-saving strategy.
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- 2022
16. Biomarkers for site-specific response to neoadjuvant chemotherapy in epithelial ovarian cancer: relating MRI changes to tumour cell load and necrosis
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Katherine Vroobel, Antonella Savio, Jennifer C. Wakefield, Susan Freeman, Khalid AbdulJabbar, Erika Pace, Jessica M. Winfield, Yinyin Yuan, James D. Brenton, Nandita M. deSouza, Shan E Ahmed Raza, Kerryn Lutchman-Singh, Susana Banerjee, Nuria Porta, Winfield, Jessica M [0000-0001-6069-5252], Brenton, James D [0000-0002-5738-6683], Ahmed Raza, Shan E [0000-0002-1097-1738], and Apollo - University of Cambridge Repository
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Cancer Research ,Pathology ,medicine.medical_specialty ,Necrosis ,Neoplasm, Residual ,medicine.medical_treatment ,Cell ,Carcinoma, Ovarian Epithelial ,Article ,030218 nuclear medicine & medical imaging ,Tumour biomarkers ,RC0254 ,03 medical and health sciences ,0302 clinical medicine ,Ovarian cancer ,Antineoplastic Combined Chemotherapy Protocols ,medicine ,Effective diffusion coefficient ,Chemotherapy ,Humans ,Prospective Studies ,Lymph node ,health care economics and organizations ,Aged ,medicine.diagnostic_test ,business.industry ,Magnetic resonance imaging ,Histology ,Middle Aged ,Debulking ,Prognosis ,Magnetic Resonance Imaging ,Neoadjuvant Therapy ,Tumor Burden ,body regions ,medicine.anatomical_structure ,Oncology ,030220 oncology & carcinogenesis ,Cancer imaging ,Female ,medicine.symptom ,business ,Biomarkers ,RC ,Follow-Up Studies - Abstract
Funder: We acknowledge funding from Cancer Research UK BIDD grant C1353/A12762 and Cancer Research UK and Engineering and Physical Sciences Research Council support to the Cancer Imaging Centre at the Institute of Cancer Research and Royal Marsden Hospital in association with the Medical Research Council and Department of Health C1060/A10334, C1060/A16464 and National Health Service funding to the National Institute for Health Research Biomedical Research Centres at Royal Marsden Hospital/Institute of Cancer Research and Cambridge, Experimental Cancer Medicine Centres, the Clinical Research Facility in Imaging, and the Cancer Research Network. We are also grateful for financial support from Addenbrooke’s Charitable Trust. The views expressed in this publication are those of the author(s) and not necessarily those of the National Health Service, the National Institute for Health Research or the Department of Health., BACKGROUND: Diffusion-weighted magnetic resonance imaging (DW-MRI) potentially interrogates site-specific response to neoadjuvant chemotherapy (NAC) in epithelial ovarian cancer (EOC). METHODS: Participants with newly diagnosed EOC due for platinum-based chemotherapy and interval debulking surgery were recruited prospectively in a multicentre study (n = 47 participants). Apparent diffusion coefficient (ADC) and solid tumour volume (up to 10 lesions per participant) were obtained from DW-MRI before and after NAC (including double-baseline for repeatability assessment in n = 19). Anatomically matched lesions were analysed after surgical excision (65 lesions obtained from 25 participants). A trained algorithm determined tumour cell fraction, percentage tumour and percentage necrosis on histology. Whole-lesion post-NAC ADC and pre/post-NAC ADC changes were compared with histological metrics (residual tumour/necrosis) for each tumour site (ovarian, omental, peritoneal, lymph node). RESULTS: Tumour volume reduced at all sites after NAC. ADC increased between pre- and post-NAC measurements. Post-NAC ADC correlated negatively with tumour cell fraction. Pre/post-NAC changes in ADC correlated positively with percentage necrosis. Significant correlations were driven by peritoneal lesions. CONCLUSIONS: Following NAC in EOC, the ADC (measured using DW-MRI) increases differentially at disease sites despite similar tumour shrinkage, making its utility site-specific. After NAC, ADC correlates negatively with tumour cell fraction; change in ADC correlates positively with percentage necrosis. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov NCT01505829.
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- 2021
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17. Breast Implant-associated Anaplastic Large Cell Lymphoma: Review and Multiparametric Imaging Paradigms
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Rajaei K. Sharma, Erika Pace, Côme Bommier, Andrew Wotherspoon, Amanda Jurgensen-Rauch, Sarkhara Sharma, Bhupinder Sharma, Ayoma D. Attygalle, Sunil Iyengar, and Dima El-Sharkawi
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medicine.medical_specialty ,CD30 ,Breast Implants ,Multimodal Imaging ,030218 nuclear medicine & medical imaging ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,law ,hemic and lymphatic diseases ,Anaplastic lymphoma kinase ,Medicine ,Mammography ,Breast MRI ,Humans ,Radiology, Nuclear Medicine and imaging ,Anaplastic large-cell lymphoma ,medicine.diagnostic_test ,business.industry ,Large cell ,medicine.disease ,030220 oncology & carcinogenesis ,Breast implant ,Lymphoma, Large-Cell, Anaplastic ,Female ,Breast disease ,Radiology ,business - Abstract
Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a new provisional category in the 2016 World Health Organization (WHO) classification of lymphoid neoplasms, and its incidence is rising owing to increasing recognition of this complication of breast implant insertion. At a median of 10 years after implant insertion, the typical presenting features are sudden-onset breast swelling secondary to peri-implant effusion and less frequently mass-forming disease. Histologic features comprise pleomorphic cells expressing CD30 and negative anaplastic lymphoma kinase (ALK) receptor, similar to systemic and cutaneous ALK-negative anaplastic large cell lymphoma (ALCL). The effusion-only subtype is generally indolent and curable with surgery, unlike the more aggressive mass-forming disease, for which systemic therapy is advocated. High clinical suspicion and pertinent use of radiologic and pathology modalities are essential for timely and accurate diagnosis of BIA-ALCL. Contemporary imaging techniques including US, mammography, breast MRI, CT, and PET/CT are routinely used in breast disease and lymphomas; however, the unique behavior of BIA-ALCL presents significant diagnostic and radiologic interpretative challenges, with numerous nuanced imaging features being pertinent, and current lymphoma staging and response guidelines are not easily applicable to BIA-ALCL. The authors evaluate available evidence in this evolving field; detail key indications, strengths, and limitations of the panoply of radiologic techniques for BIA-ALCL; and propose multiparametric imaging paradigms for management of the peri-implant effusion and mass-forming or advanced disease subtypes, with the goal of accurate optimal patient care. The authors also predict a future model of multimodal assessment using novel imaging and molecular techniques and define key research directions. ©RSNA, 2020.
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- 2020
18. Variation of the apparent diffusion coefficient of skull bone marrow by age group, pubertal status, and gender in a pediatric population
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Erika Pace, Nandita M. deSouza, and Andrew D MacKinnon
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Male ,Radiological and Ultrasound Technology ,Adolescent ,business.industry ,Skull ,Physiology ,General Medicine ,Diffusion-Weighted Magnetic Resonance Imaging ,body regions ,medicine.anatomical_structure ,Diffusion Magnetic Resonance Imaging ,Sex Factors ,Clivus ,Bone Marrow ,Child, Preschool ,medicine ,Effective diffusion coefficient ,Skull bone ,Humans ,Radiology, Nuclear Medicine and imaging ,Female ,Bone marrow ,business ,Child ,Pediatric population - Abstract
Background Bone marrow composition varies with stage of development. Purpose To assess differences in apparent diffusion coefficient (ADC) derived from clivus bone marrow in healthy children by age, pubertal status, and gender as a benchmark when monitoring local and systemic treatment-induced effects. Material and Methods Non-oncological pediatric patients (30 pre-pubertal [15 girls, 15 boys] and 30 post-pubertal [15 girls, 15 boys]) with previous normal magnetic resonance imaging (MRI) of the brain including diffusion-weighted magnetic resonance imaging (DW-MRI; 1.5-T Philips Achieva-Ingenia, b-values 0 and 1000s/mm2) were studied. A 4–6 mm diameter region of interest (ROI), drawn within the clivus on two or three DW-MRI slices, yielded mean and centile ADC values. Pubertal status was recognized from imaging appearances of the pituitary gland and from fusion of the spheno-occipital synchondrosis. Correlations between ADC and age were assessed (Pearson’s coefficient). Mann–Whitney U tests compared ADC by age, pubertal status, and gender. Results Age and ADC were significantly negatively correlated (median ADC r=–0.48, mean ADC r=–0.42, P=0.0001 and 0.0008, respectively) which held true when divided by gender. Mean and median ADC differed significantly before and after puberty for the whole population ( P=0.0001 and 0.0001, respectively). There was a left shift of the ADC histogram after puberty with significant differences in centile values. ADC differences before and after puberty remained when divided by gender (girls: P=0.04 and 0.009, respectively; boys: P=0.005 and 0.0002, respectively). Conclusion ADC of clivus bone marrow correlates with age in children. ADC decreases significantly after puberty, likely due to replacement of hypercellular marrow with fat. There are no gender-related differences in clivus bone-marrow ADC before or after puberty.
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- 2019
19. Diagnosis, treatment and outcome of hepatic venous outflow obstruction in paediatric liver transplantation: 24-year experience at a single centre
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Stéphanie Franchi-Abella, Emmanuel Gonzales, Alexis Galloux, Sophie Branchereau, Erika Pace, and Danièle Pariente
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Graft Rejection ,Male ,medicine.medical_specialty ,Adolescent ,medicine.medical_treatment ,Venography ,Budd-Chiari Syndrome ,030230 surgery ,Liver transplantation ,Inferior vena cava ,03 medical and health sciences ,Postoperative Complications ,0302 clinical medicine ,Angioplasty ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Child ,Vein ,Retrospective Studies ,medicine.diagnostic_test ,business.industry ,Incidence ,Infant ,medicine.disease ,Liver Transplantation ,Surgery ,Transplantation ,Stenosis ,surgical procedures, operative ,medicine.anatomical_structure ,medicine.vein ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,cardiovascular system ,Budd–Chiari syndrome ,Female ,Stents ,030211 gastroenterology & hepatology ,business ,Angioplasty, Balloon - Abstract
Hepatic venous outflow obstruction after paediatric liver transplantation is an unusual but critical complication. To review the incidence, diagnosis and therapeutic modalities of hepatic venous outflow obstruction from a large national liver transplant unit. During the period from October 1992 to March 2016, 917 liver transplant procedures were performed with all types of grafts in 792 children. Transplants suspected to have early or delayed venous outflow obstruction were confirmed by percutaneous venography or surgical revision findings. Therapeutic intervention, recurrence and outcome were evaluated. Twenty-six of 792 children (3.3%) experienced post-transplant hepatic venous outflow obstruction. These patients had been diagnosed from 1 day to 8.75 years after transplantation. Six occurred during the early post-transplant period; in three of them, the graft was lost. Seventeen patients were initially treated by balloon angioplasty with success; 11 of these experienced recurrences. Four stents were implanted; one was complicated by definitive occlusion. Three of the five surgical revisions were successful. The initial stenosis involved the inferior vena cava in 10 grafts, in isolation or associated with hepatic vein involvement. Mean follow-up was 79 months after transplantation. Eight grafts were lost. Acute postoperative hepatic venous outflow obstruction was associated with poor prognosis. Diagnostic venography should be performed if there is any suspicion of venous outflow obstruction, even if first-line examinations are normal. Stenosis frequently involved the inferior vena cava. Angioplasty was a safe and efficient treatment for venous outflow obstruction despite frequent recurrence.
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- 2018
20. Benign biliary diseases
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Maria Antonietta Bali, Martina Pezzullo, Mario Morone, and Erika Pace
- Subjects
Male ,medicine.medical_specialty ,Cholangiopancreatography, Magnetic Resonance ,Biliary Tract Diseases ,Gallbladder disease ,Contrast Media ,Gallbladder Diseases ,Malignancy ,030218 nuclear medicine & medical imaging ,Primary sclerosing cholangitis ,Diagnosis, Differential ,03 medical and health sciences ,Postoperative Complications ,0302 clinical medicine ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Biliary Tract ,Cholangiopancreatography, Endoscopic Retrograde ,Magnetic resonance cholangiopancreatography ,medicine.diagnostic_test ,business.industry ,Mr contrast agent ,Magnetic resonance imaging ,General Medicine ,medicine.disease ,Magnetic Resonance Imaging ,Biliary tract ,Female ,030211 gastroenterology & hepatology ,Radiology ,Differential diagnosis ,business - Abstract
Benign biliary diseases include a large spectrum of congenital and acquired disorders, which have different prognosis and require different treatment management. The diagnosis may be challenging since some benign disorders may mimic malignancy. Imaging has an important role in the diagnostic process, for treatment decision and planning and in patient follow up. Magnetic resonance (MR) with magnetic resonance cholangiopancreatography (MRCP) sequences is the imaging modality of choice for biliary diseases and has demonstrated high diagnostic accuracy. Moreover, the use of a hepato-specific MR contrast agent allows morphological and functional assessment of the liver and the biliary tree improving the diagnostic performance.
- Published
- 2017
21. Breast implant associated anaplastic large cell lymphoma
- Author
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Erika Pace, Bhupinder Sharma, Olubanke Davies, and Fiona MacNeill
- Subjects
medicine.diagnostic_test ,business.industry ,Computed tomography ,General Medicine ,030204 cardiovascular system & hematology ,medicine.disease ,law.invention ,body regions ,03 medical and health sciences ,0302 clinical medicine ,law ,Positron emission tomography ,Seroma ,Breast implant ,medicine ,030212 general & internal medicine ,business ,Nuclear medicine ,Anaplastic large-cell lymphoma - Abstract
This is an image from a positron emission tomography/computed tomography (PET/CT) scan (fig 1) showing a large photopenic seroma (red arrow) surrounding an intact breast implant …
- Published
- 2019
22. Opportunities and Challenges for Paediatric Radiology Service Development in the National Health Service within the United Kingdom
- Author
-
Erika Pace
- Published
- 2016
23. Obscure and occult gastrointestinal bleeding: comparison of different imaging modalities
- Author
-
Angelo Milano, Roberta Cianci, Matteo Neri, Antonella Filippone, Erika Pace, and Antonio Raffaele Cotroneo
- Subjects
medicine.medical_specialty ,Gastrointestinal bleeding ,Urology ,Contrast Media ,Colonoscopy ,Capsule Endoscopy ,Endoscopy, Gastrointestinal ,law.invention ,Capsule endoscopy ,law ,Double-balloon enteroscopy ,Multidetector Computed Tomography ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Radiological and Ultrasound Technology ,medicine.diagnostic_test ,business.industry ,Esophagogastroduodenoscopy ,Gastroenterology ,General Medicine ,medicine.disease ,Magnetic Resonance Imaging ,Occult ,Endoscopy ,Etiology ,Radiology ,Gastrointestinal Hemorrhage ,Tomography, X-Ray Computed ,business - Abstract
Patients with persistent, recurrent, or intermittent bleeding from the gastrointestinal (GI) tract for which no definite cause has been identified by initial esophagogastroduodenoscopy, colonoscopy, or conventional radiologic evaluation are considered to have an obscure GI bleeding (OGIB). The diagnosis and management of patients with OGIB is challenging, often requiring extensive and expensive workups. The main objective is the identification of the etiology and site of bleeding, which should be as rapidly accomplished as possible, in order to establish the most appropriate therapy. The introduction of capsule endoscopy and double balloon enteroscopy and the recent improvements in CT and MRI techniques have revolutionized the approach to patients with OGIB, allowing the visualization of the entire GI tract, particularly the small bowel, until now considered as the "dark continent" . In this article we review and compare the radiologic and endoscopic examinations currently used in occult and OGIB, focusing on diagnostic patterns, pitfalls, strengths, weaknesses, and value in patients' management.
- Published
- 2011
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