Related Experiment Video
Updated: Jun 26, 2025

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
Large-vessel vasculitis possibly induced by BRAF and MEK inhibitors for BRAF V600E positive lung adenocarcinoma
Kento Ichikawa1, Shigeru Ohno2, Sousuke Kubo3
1Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama, Japan ichikawa.ken.jn@yokohama-cu.ac.jp.
Abstract:
The combination therapy of v-Raf murine sarcoma viral oncogene homolog B1 (BRAF) and mitogen-activated protein kinase kinase (MEK) inhibitors is approved for treating patients with BRAF V600E-positive tumours, including melanoma and lung cancer. Several case reports indicated autoimmune side effects associated with the use of BRAF and MEK inhibitors. Still, the effects of these drugs on the immune system were not fully elucidated. Here, we report a patient with large-vessel vasculitis diagnosed after initiation of treatment with dabrafenib and trametinib for BRAF V600E-positive metastatic lung adenocarcinoma. She was a never-smoker woman in her early 70s who presented with a chronic cough and was diagnosed with BRAF V600E-positive metastatic lung adenocarcinoma by transbronchial lung biopsy. She was successfully treated with prednisolone and methotrexate while BRAF and MEK inhibitors were continued. We should be careful about autoimmune diseases using BRAF and MEK inhibitors.
Insights
BRAF and MEK inhibitors can cause autoimmune diseases like vasculitis in lung cancer patients. Careful monitoring for immune side effects is crucial during combination therapy.
Area of Science:
- Oncology
- Immunology
- Rheumatology
Background:
- BRAF and MEK inhibitors are approved for BRAF V600E-positive cancers.
- Autoimmune side effects have been reported with these inhibitors.
- The precise impact on the immune system remains unclear.

