Targeted therapy for rare BRAF-mutated melanoma: Updated multicenter analysis and launch of a publicly accessible

Christian Menzer1, Susanne Dugas-Breit1, Martin Dugas2

  • 1Heidelberg University, Medical Faculty Heidelberg, Department of Dermatology and National Center for Tumor Diseases (NCT), NCT Heidelberg, A Partnership Between DKFZ and University Hospital Heidelberg, Heidelberg, Germany.

European Journal of Cancer (Oxford, England : 1990)
|August 24, 2025
PubMed
Abstract

Insights

BRAF-/MEK-inhibitor therapy shows efficacy in advanced melanoma with rare BRAF mutations. Combination therapy offers the best outcomes, and a global database for rare BRAF mutations is now available.

Area of Science:

  • Oncology
  • Genetics
  • Dermatology

Background:

  • BRAF-/MEK-inhibitor therapy is standard for V600E/K-mutated melanoma.
  • Efficacy in advanced melanoma with rare BRAF mutations is uncertain.
  • This study analyzes an international data collection of 49 new patients with rare BRAF mutations.

Purpose of the Study:

  • To evaluate the efficacy of BRAF-/MEK-inhibitor therapy in advanced melanoma with rare BRAF mutations.
  • To compare outcomes between BRAF V600 (V600-nonE/K) and non-V600 mutations.
  • To develop a publicly accessible global database for rare BRAF mutations.

Main Methods:

  • Retrospective analysis of 143 patients from 20 international cancer centers.
  • Evaluation of BRAF/MEK inhibitor combination therapy (BRAFi/MEKi) and monotherapies.
  • Collection of clinical outcomes including overall response rate (ORR), progression-free survival (PFS), and overall survival (OS).

Main Results:

  • Overall response rate (ORR) was 35%, higher in V600-nonE/K (45%) than non-V600 melanomas (26%).
  • Combination therapy (BRAFi/MEKi) showed the best results in both groups.
  • Patients with specific rare mutations (V600D/R, V600_K601D/E/N, K601E/N-, L597V/S/R/Q/P/K-) had the longest PFS (>50 months).

Conclusions:

  • BRAF-/MEK-inhibitor therapy is beneficial for rare BRAF mutations in advanced melanoma.
  • Combination therapy is recommended for optimal outcomes.
  • A database for ongoing data collection on rare BRAF mutations has been established.