Literature DB >> 32720072

BRAF Inhibitors for the Treatment of Papulopustular Eruptions from MAPK Pathway Inhibitors.

Catherine J Wang1, Isaac Brownell2.   

Abstract

Inhibitors of the mitogen-activated protein kinase (MAPK) pathway are commonly used in clinical oncology. However, with the exception of BRAF inhibitors (BRAFi), MAPK pathway inhibitors such as epidermal growth factor receptor inhibitors (EGFRi) or MEK inhibitors (MEKi) are associated with dose-limiting papulopustular eruptions. Interestingly, patients treated with a combination of systemic BRAFi and MEKi experience less skin toxicities than patients on monotherapy BRAFi or MEKi. The reduction in cutaneous adverse events with combination therapy is thought to be due to a paradoxical activation of the MAPK pathway by BRAFi in keratinocytes carrying wildtype BRAF. Although treatment options for EGFRi- or MEKi-induced papulopustular eruptions exist, many patients still experience dose reduction, interruption, or discontinuation of EGFRi or MEKi. With the goal of activating MAPK signaling in the skin via BRAFi while minimizing systemic risks, we propose topical BRAFi therapy for the treatment and prevention of papulopustular eruptions due to MAPK pathway inhibitors. If effective, patients will be able to tolerate higher doses of MAPK pathway inhibitors, stay on treatment longer, and achieve better therapeutic outcomes overall.

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Year:  2020        PMID: 32720072      PMCID: PMC7680264          DOI: 10.1007/s40257-020-00539-7

Source DB:  PubMed          Journal:  Am J Clin Dermatol        ISSN: 1175-0561            Impact factor:   7.403


  25 in total

1.  Prognostic value of cetuximab-related skin toxicity in metastatic colorectal cancer patients and its correlation with parameters of the epidermal growth factor receptor signal transduction pathway: results from a randomized trial of the GERMAN AIO CRC Study Group.

Authors:  Sebastian Stintzing; Christine Kapaun; Rüdiger Paul Laubender; Andreas Jung; Jens Neumann; Dominik Paul Modest; Clemens Giessen; Nicolas Moosmann; Andreas Wollenberg; Thomas Kirchner; Volker Heinemann
Journal:  Int J Cancer       Date:  2012-06-26       Impact factor: 7.396

2.  Pilot trial of combined BRAF and EGFR inhibition in BRAF-mutant metastatic colorectal cancer patients.

Authors:  Rona Yaeger; Andrea Cercek; Eileen M O'Reilly; Diane L Reidy; Nancy Kemeny; Tamar Wolinsky; Marinela Capanu; Marc J Gollub; Neal Rosen; Michael F Berger; Mario E Lacouture; Efsevia Vakiani; Leonard B Saltz
Journal:  Clin Cancer Res       Date:  2015-01-14       Impact factor: 12.531

Review 3.  Advances in the management of cutaneous toxicities of targeted therapies.

Authors:  Caroline Robert; Vincent Sibaud; Christine Mateus; Basil S Cherpelis
Journal:  Semin Oncol       Date:  2012-04       Impact factor: 4.929

4.  Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF.

Authors:  Sonja J Heidorn; Carla Milagre; Steven Whittaker; Arnaud Nourry; Ion Niculescu-Duvas; Nathalie Dhomen; Jahan Hussain; Jorge S Reis-Filho; Caroline J Springer; Catrin Pritchard; Richard Marais
Journal:  Cell       Date:  2010-01-22       Impact factor: 41.582

5.  Correlation between development of rash and efficacy in patients treated with the epidermal growth factor receptor tyrosine kinase inhibitor erlotinib in two large phase III studies.

Authors:  Bret Wacker; Tina Nagrani; Jacqueline Weinberg; Karsten Witt; Gary Clark; Pablo J Cagnoni
Journal:  Clin Cancer Res       Date:  2007-07-01       Impact factor: 12.531

6.  Binimetinib, Encorafenib, and Cetuximab Triplet Therapy for Patients With BRAF V600E-Mutant Metastatic Colorectal Cancer: Safety Lead-In Results From the Phase III BEACON Colorectal Cancer Study.

Authors:  Eric Van Cutsem; Sanne Huijberts; Axel Grothey; Rona Yaeger; Pieter-Jan Cuyle; Elena Elez; Marwan Fakih; Clara Montagut; Marc Peeters; Takayuki Yoshino; Harpreet Wasan; Jayesh Desai; Fortunato Ciardiello; Ashwin Gollerkeri; Janna Christy-Bittel; Kati Maharry; Victor Sandor; Jan H M Schellens; Scott Kopetz; Josep Tabernero
Journal:  J Clin Oncol       Date:  2019-03-20       Impact factor: 44.544

Review 7.  Skin rash could predict the response to EGFR tyrosine kinase inhibitor and the prognosis for patients with non-small cell lung cancer: a systematic review and meta-analysis.

Authors:  Hong-bing Liu; Ying Wu; Tang-feng Lv; Yan-wen Yao; Yong-ying Xiao; Dong-mei Yuan; Yong Song
Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

8.  Hair eruption initiates and commensal skin microbiota aggravate adverse events of anti-EGFR therapy.

Authors:  Jörg Klufa; Thomas Bauer; Buck Hanson; Craig Herbold; Philipp Starkl; Beate Lichtenberger; Dagmar Srutkova; Daniel Schulz; Igor Vujic; Thomas Mohr; Klemens Rappersberger; Bernd Bodenmiller; Hana Kozakova; Sylvia Knapp; Alexander Loy; Maria Sibilia
Journal:  Sci Transl Med       Date:  2019-12-11       Impact factor: 19.319

9.  Synchronous BRAF(V600E) and MEK inhibition leads to superior control of murine melanoma by limiting MEK inhibitor induced skin toxicity.

Authors:  Jules Gadiot; Anna I Hooijkaas; Marcel A Deken; Christian U Blank
Journal:  Onco Targets Ther       Date:  2013-11-28       Impact factor: 4.147

10.  Incidence and relative risk of cutaneous squamous cell carcinoma with single-agent BRAF inhibitor and dual BRAF/MEK inhibitors in cancer patients: a meta-analysis.

Authors:  Ling Peng; Yina Wang; Yun Hong; Xianghua Ye; Peng Shi; Junyan Zhang; Qiong Zhao
Journal:  Oncotarget       Date:  2017-09-19
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