Clinical efficacy and cardiac toxicity associated with first-line dabrafenib plus trametinib in advanced BRAF V600_K601delinsE-mutated lung adenocarcinoma: a case report and literature review

The BRAF V600_K601delinsE (c.1799_1801del) mutation is rare, with an estimated prevalence of 0.05% among all tumor types. Therapeutic options for advanced lung adenocarcinoma harboring this mutation are limited. We present a case of a patient with advanced lung adenocarcinoma carrying the BRAF V600_K601delinsE mutation who derived clinical benefit for one year from treatment with dabrafenib plus trametinib. The patient subsequently developed biventricular asynergy and a significant reduction in left ventricular ejection fraction (LVEF). This case of drug-induced cardiomyopathy is presented in the context of this known adverse reaction, which affects nearly 6% of patients receiving this combination regimen. This report contributes experience on the management of this rare genomic subtype and offers perspectives on addressing its associated adverse drug reactions.

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Publication Details

Journal
Discover Oncology
Published
2026-02-09
DOI
https://doi.org/10.1007/s12672-026-04607-y
Citations
1
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
36.44
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article

Clinical efficacy and cardiac toxicity associated with first-line dabrafenib plus trametinib in advanced BRAF V600_K601delinsE-mutated lung adenocarcinoma: a case report and literature review

W F Liu, BaoShan Cao, X H Liu, Lina Yang et al.
1 citations
Discover Oncology
Lung Cancer Treatments and Mutations
36.44
article

Clinical efficacy and cardiac toxicity associated with first-line dabrafenib plus trametinib in advanced BRAF V600_K601delinsE-mutated lung adenocarcinoma: a case report and literature review

W F Liu, BaoShan Cao, X H Liu, Lina Yang, Xiang Zhu, Yangchun Gu
article en
1 citations

Abstract

The BRAF V600_K601delinsE (c.1799_1801del) mutation is rare, with an estimated prevalence of 0.05% among all tumor types. Therapeutic options for advanced lung adenocarcinoma harboring this mutation are limited. We present a case of a patient with advanced lung adenocarcinoma carrying the BRAF V600_K601delinsE mutation who derived clinical benefit for one year from treatment with dabrafenib plus trametinib. The patient subsequently developed biventricular asynergy and a significant reduction in left ventricular ejection fraction (LVEF). This case of drug-induced cardiomyopathy is presented in the context of this known adverse reaction, which affects nearly 6% of patients receiving this combination regimen. This report contributes experience on the management of this rare genomic subtype and offers perspectives on addressing its associated adverse drug reactions.

Discover OncologyVol. 17(1)
Peking University (CN), The People's Hospital of Guangxi Zhuang Autonomous Region (CN), Peking University Third Hospital (CN)
Good health and well-being
Openalex Percentile: Top 1%
Lung Cancer Treatments and Mutations
36.44
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