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      Characterization and Outcomes of Disease Progression in 52 Patients Treated with BRAF -V600 + MEK Inhibitors for Advanced Melanoma

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          Abstract

          Background: Combined treatment with BRAF-V600 and MEK inhibitors has significantly improved progression-free and overall survival of patients with BRAF-mutated melanoma. Pattern of disease progression and outcomes in patients have not been fully characterized. Methods: We conducted a single-center, retrospective, descriptive analysis of a cohort of 52 patients treated with BRAF-V600 + MEK inhibitors for advanced melanoma over a 12-month period. The aim of this study was to characterize disease progression, defined as metastatic pattern, disease kinetics, and response to subsequent therapies, in melanoma patients treated with BRAF-V600 + MEK inhibitors. Results: Disease progression was observed in 31/52 (59.6%) patients treated with BRAF-V600 + MEK inhibitors. Relapse of melanoma involved the CNS for 22/31 (70.9%) patients with disease progression, including 18/31 (58%) patients who had exclusive intracranial metastases. Sixteen patients died from disease progression. Among the 31 patients who had disease progression, the median time until a relapse was 8 months, and the median survival time after disease progression was 2 months. Conclusion: Our study shows that, for patients treated with BRAF-V600 + MEK inhibitors who lose response, disease progression was aggressive and had poor outcomes. Most patients had CNS metastases and low rates of therapeutic response to any subsequent therapy.

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          Author and article information

          Journal
          DRM
          Dermatology
          10.1159/issn.1018-8665
          Dermatology
          S. Karger AG
          1018-8665
          1421-9832
          2018
          September 2018
          15 August 2018
          : 234
          : 3-4
          : 92-98
          Affiliations
          Toulouse University Institute of Cancer, Toulouse, France
          Author notes
          *Prof. Nicolas Meyer, Dermatology, Paul Sabatier Toulouse III University, Larrey Hospital and Toulouse University Institute of Cancer, 24, chemin de Pouvourville, FR–31059 Toulouse Cedex (France), E-Mail Meyer.n@chu-toulouse.fr
          Author information
          https://orcid.org/0000-0003-4519-8666
          Article
          490891 Dermatology 2018;234:92–98
          10.1159/000490891
          30110681
          f69ec9b1-8f42-47d7-ab1a-df211a3c5182
          © 2018 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

          History
          : 21 March 2018
          : 14 June 2018
          Page count
          Figures: 3, Tables: 3, Pages: 7
          Categories
          Skin Cancer - Original Paper

          Oncology & Radiotherapy,Pathology,Surgery,Dermatology,Pharmacology & Pharmaceutical medicine
          BRAF inhibitor,MEK inhibitor,Dabrafenib,Melanoma,Vemurafenib

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