8 results on '"Philipp Harter"'
Search Results
2. Pelvic Lymphadenectomy in Vulvar Cancer – Does it make sense?
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Barbara Schmalfeldt, Eik Vettorazzi, Linn Woelber, Werner Meier, Katharina Prieske, Pauline Wimberger, Martin Hellriegel, Mareike Bommert, Niko de Gregorio, Tanja Fehm, Jalid Sehouli, Ulrich Canzler, Hans-Georg Strauss, Christoph Heiss, Inger Fischer, Alexander Luyten, Philipp Harter, J Kosse, Peter Mallmann, Berno Tanner, Felix Hilpert, Atanas Ignatov, Lars Hanker, Julia Kathrin Jueckstock, Anna Jaeger, Sven Mahner, Peer Hantschmann, Matthias W. Beckmann, Peter Hillemanns, Klaus Baumann, Severine Iborra, Alexander Mustea, Jacobus Pfisterer, Christine Eulenburg, and Sophie Fuerst
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medicine.medical_specialty ,recurrence ,Population ,Lymphknotenmetastasen ,pelvine Lymphonodektomie ,Prognose ,Metastasis ,03 medical and health sciences ,Vulvakarzinom ,0302 clinical medicine ,Maternity and Midwifery ,medicine ,Review/Übersicht ,GebFra Science ,Stage (cooking) ,pelvic lymphadenectomy ,education ,Lymph node ,education.field_of_study ,vulvar cancer ,030219 obstetrics & reproductive medicine ,lymph node metastasis ,Groin ,business.industry ,Obstetrics and Gynecology ,Guideline ,Vulvar cancer ,medicine.disease ,3. Good health ,body regions ,medicine.anatomical_structure ,Rezidiv ,030220 oncology & carcinogenesis ,prognosis ,Radiology ,Lymph ,business - Abstract
Since the publication of the updated German guideline in 2015, the recommendations for performing pelvic lymphadenectomy (LAE) in patients with vulvar cancer (VSCC) have changed considerably. The guideline recommends surgical lymph node staging in all patients with a higher risk of pelvic lymph node involvement. However, the current data do not allow the population at risk to be clearly defined, therefore, the indication for pelvic lymphadenectomy is still not clear. There are currently two published German patient populations who had pelvic LAE which can be used to investigate both the prognostic effect of histologically verified pelvic lymph node metastasis and the relation between inguinal and pelvic lymph node involvement. A total of 1618 patients with primary FIGO stage ≥ IB VSCC were included in the multicenter AGO CaRE-1 study (1998 – 2008), 70 of whom underwent pelvic LAE. During a retrospective single-center evaluation carried out at the University Medical Center Hamburg-Eppendorf (UKE), a total of 514 patients with primary VSCC treated between 1996 – 2018 were evaluated, 21 of whom underwent pelvic LAE. In both cohorts, around 80% of the patients who underwent pelvic LAE were inguinally node-positive, with a median number of three affected groin lymph nodes. There were no cases of pelvic lymph node metastasis without inguinal lymph node metastasis in either of the two cohorts. Between 33 – 35% of the inguinal node-positive patients also had pelvic lymph node metastasis; the median number of affected groin lymph nodes in these patients was high (> 4), and the maximum median diameter of the largest inguinal metastasis was > 40 mm in both cohorts. Pelvic lymph node staging and pelvic radiotherapy is therefore probably not necessary for the majority of node-positive patients with VSCC, as the relevant risk of pelvic lymph node involvement was primarily found in node-positive patients with high-grade disease. More, ideally prospective data collections are necessary to validate the relation between inguinal and pelvic lymph node involvement.
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- 2020
3. Prevalence of BRCA1 and BRCA2 Mutations in Patients with Primary Ovarian Cancer – Does the German Checklist for Detecting the Risk of Hereditary Breast and Ovarian Cancer Adequately Depict the Need for Consultation?
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Rita K. Schmutzler, Alexander Traut, Kerstin Rhiem, S Ehmann, Philipp Harter, Andreas du Bois, Thaïs Baert, Stephanie Schneider, Denise Tripon, N Pauly, Helmut Plett, Beyhan Ataseven, and Florian Heitz
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0301 basic medicine ,MAINTENANCE THERAPY ,PENETRANCE ,medicine.medical_specialty ,endocrine system diseases ,SCORING SYSTEM ,Genetic counseling ,MODELS ,Population ,hereditary breast and ovarian cancer ,GERMLINE BRCA1 ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Maternity and Midwifery ,medicine ,education ,heritability checklist ,Genetic testing ,education.field_of_study ,Science & Technology ,CARRIER PROBABILITIES ,medicine.diagnostic_test ,business.industry ,BRCA mutation ,Obstetrics & Gynecology ,WOMEN ,Obstetrics and Gynecology ,ASSOCIATION ,SERIES ,medicine.disease ,Checklist ,ovarian cancer ,030104 developmental biology ,030220 oncology & carcinogenesis ,Cohort ,Mutation (genetic algorithm) ,BOADICEA ,business ,Ovarian cancer ,Life Sciences & Biomedicine - Abstract
Background BRCA1/2 mutations are the leading cause of hereditary epithelial ovarian cancer (EOC). The German Consortium for Hereditary Breast and Ovarian Cancer has defined inclusion criteria, which are retrievable as a checklist and facilitate genetic counselling/testing for affected persons with a mutation probability of ≥ 10%. Our objective was to evaluate the prevalence of the BRCA1/2 mutation(s) based on the checklist score (CLS). Methods A retrospective data analysis was performed on EOC patients with a primary diagnosis treated between 1/2011 – 5/2019 at the Central Essen Clinics, where a BRCA1/2 genetic analysis result and a CLS was available. Out of 545 cases with a BRCA1/2 result (cohort A), 453 cases additionally had an extended gene panel result (cohort B). Results A BRCA1/2 mutation was identified in 23.3% (127/545) in cohort A, pathogenic mutations in non-BRCA1/2 genes were revealed in a further 6.2% in cohort B. In cohort A, 23.3% (127/545) of patients had a BRCA1 (n = 92) or BRCA2 (n = 35) mutation. Singular EOC (CLS 2) was present in 40.9%. The prevalence for a BRCA1/2 mutation in cohort A was 10.8%, 17.2%, 25.0%, 35.1%, 51.4% and 66.7% for patients with CLS 2, 3, 4, 5, 6 and ≥ 7 respectively. The mutation prevalence in cohort B was 15.9%, 16.4%, 28.2%, 40.4%, 44.8% and 62.5% for patients with CLS 2, 3, 4, 5, 6 and ≥ 7 respectively. Conclusions The BRCA1/2 mutation prevalence in EOC patients positively correlates with a rising checklist score. Already with singular EOC, the prevalence of a BRCA1/2 mutation exceeds the required 10% threshold. Our data support the recommendation of the S3 guidelines Ovarian Cancer of offering genetic testing to all patients with EOC. Optimisation of the checklist with clear identification of the testing indication in this population should therefore be aimed for.
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- 2020
4. Gynäkologische Tumoren – Therapie und Prognosefaktoren uteriner Sarkome – Was ist neu?
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Florian Heitz, Mareike Sporkmann, and Philipp Harter
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Maternity and Midwifery ,Obstetrics and Gynecology - Published
- 2016
5. Alienor/Engot-Ov7 – Eine randomisierte Phase-II-Studie bei rezidiviertem Keimstrangstroma-Tumor (SCT) mit Bevacizumab (Bev) in Kombination mit wöchentlichem Paclitaxel versus wöchentlichem Paclitaxel allein (wPac)
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HJ Lück, Philipp Harter, Andreas Schnelzer, Sophie Fürst, Jalid Sehouli, and I.L. Ray-Coquard
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- 2019
6. Low-grade Serous Ovarian Carcinoma
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Thaïs Baert, Florian Heitz, Beyhan Ataseven, Philipp Harter, Mareike Bommert, Enzo Ricciardi, Stephanie Schneider, Sonia Prader, and Andreas du Bois
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Oncology ,seltener Tumor ,medicine.medical_specialty ,MAINTENANCE THERAPY ,endocrine system diseases ,BEVACIZUMAB ,Ovary ,Subgroup analysis ,Review ,03 medical and health sciences ,DOUBLE-BLIND ,0302 clinical medicine ,Ovarian carcinoma ,Internal medicine ,Maternity and Midwifery ,medicine ,Serous ovarian cancer ,GebFra Science ,rare tumour ,low-grade serous ,030219 obstetrics & reproductive medicine ,Low-grade serös ,Science & Technology ,PHASE-3 TRIAL ,business.industry ,Obstetrics and Gynecology ,Obstetrics & Gynecology ,WOMEN ,CHEMOTHERAPY ,medicine.disease ,TUMORS ,female genital diseases and pregnancy complications ,PEGYLATED LIPOSOMAL DOXORUBICIN ,Clinical trial ,Serous fluid ,medicine.anatomical_structure ,ovarian cancer ,030220 oncology & carcinogenesis ,SURVIVAL ,Ovarialkarzinom ,PERITONEAL CANCER ,business ,Ovarian cancer ,Life Sciences & Biomedicine - Abstract
In the early 2000s a two-tier grading system was introduced for serous ovarian cancer. Since then, we have increasingly come to accept that low-grade serous ovarian carcinoma (LGSOC) is a separate entity with a unique mutational landscape and clinical behaviour. As less than 10% of serous carcinomas of the ovary are low-grade, they are present in only a small number of patients in clinical trials for ovarian cancer. Therefore the current treatment of LGSOC is based on smaller trials, retrospective series, and subgroup analysis of large clinical trials on ovarian cancer. Surgery plays a major role in the treatment of patients with LGSOC. In the systemic treatment of LGSOC, hormonal treatment and targeted therapies seem to play an important role.Kurz nach der Jahrtausendwende wurde ein 2-stufiges Klassifizierungssystem zur Einstufung von serösen Ovarialkarzinomen eingeführt. Seither wird zunehmend akzeptiert, dass das Low-grade seröse Ovarialkarzinom (LGSOC) eine eigenständige Einheit mit eigener Mutationslandschaft und klinischem Verhalten bildet. Weniger als 10% aller serösen Karzinome des Ovars werden dem Low-Grade-Subtyp zugeordnet, und in den klinischen Studien zum Ovarialkrebs tritt diese Form nur in wenigen Patientinnen auf. Die aktuelle Therapie für das LGSOC basiert daher auf den Ergebnissen kleinerer Studien und retrospektiver Serien sowie auf der Subgruppenanalyse von großen klinischen Studien zum Ovarialkarzinom. Die operative Therapie spielt eine wichtige Rolle für die Behandlung von Patientinnen mit LGSOC. Bei der systemischen Therapie des LGSOC scheinen sowohl hormonelle Therapien als auch gezielte Therapien eine wichtige Rolle zu spielen.
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- 2018
7. Seltene Tumoren: mesenchymale Tumoren des Uterus
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Philipp Harter, Beyhan Ataseven, Andreas du Bois, and Florian Heitz
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- 2015
8. Sarcoma of the Uterus. Guideline of the DGGG (S2k-Level, AWMF Registry No. 015/074, August 2015)
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Peter Mallmann, T. Vogl, Sven Ackermann, Dominik Denschlag, Philipp Harter, Dietmar Schmidt, M. W. Beckmann, M. Gebhardt, Dirk Vordermark, Falk Thiel, I Juhasz-Boess, Peter Reichardt, Uwe Ulrich, L.-C. Horn, HG Strauss, and P. Gaß
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Leiomyosarcoma ,Gynecology ,medicine.medical_specialty ,Endometrial stromal sarcoma ,Uterine sarcoma ,business.industry ,General surgery ,Obstetrics and Gynecology ,Guideline ,medicine.disease ,Article ,Systematic review ,Maternity and Midwifery ,Adenosarcoma ,Carcinosarcoma ,medicine ,Sarcoma ,business - Abstract
Purpose: Official guideline published and coordinated by the German Society of Gynecology and Obstetrics (DGGG). Due to their rarity and their heterogeneous histopathology uterine sarcomas remain challenging tumors to manage and need a multidisciplinary approach. To our knowledge so far there is no evidence-based guideline on the appropiate management of these heterogeneous tumors. Methods: This S2k-guideline is the work of an representative committee of experts from a variety of different professions who were commissioned by the DGGG to carry out a systematic literature review of uterine sarcoma. Members of the participating scientific societies developed a structured consensus in a formal procedure. Recommendations: 1. The incidence and histopathologic classification of uterine sarcoma. 2. The clinical manifestations, diagnosis and staging of uterine sarcoma. 3. The management of leiomyosarcoma. 4. The management of endometrial stromal sarcoma and undifferentiated uterine sarcoma. 5. The management of adenosarcoma as well as carcinosarcomas. 6. The management of morcellated uterine sarcoma
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- 2015
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