Diversity of BRAF mutations in non-small cell lung cancer and implications on treatment

The optimal treatment sequence in non-small cell lung cancer harboring class I BRAF mutations and atypical BRAF variants remains unclear. To better characterize therapeutic strategy, we retrospectively evaluated a multi-institutional cohort of BRAF-mutant NSCLC patients (n = 97) and an independent clinico-genomic database (n = 342), performed structural modeling, and conducted chemical screens of BRAF-mutant cell lines. Patients with class I BRAF mutation treated with BRAF-MEK inhibitors at any line of therapy had significantly greater median overall survival compared to those who did not receive BRAF-MEK inhibitors (40 vs 10 months, Log-rank p = 0.043). There, however, was no significant survival difference between patients treated with immune checkpoint inhibitors versus those not treated. Tumors with class II or III BRAF variants were significantly more likely to harbor concurrent MAPK pathway alterations relative to class I (Chi-Square p < 10<sup>-4</sup>). Cell line studies identified genetic dependency on BRAF in class II cell lines without sensitivity to BRAF inhibitors, and dependency on EGFR in class III cell lines.

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Publication Details

Journal
npj Precision Oncology
Published
2025-10-28
DOI
https://doi.org/10.1038/s41698-025-01089-z
Citations
1
Primary Topic
Melanoma and MAPK Pathways
Type
article
Field-Weighted Citation Impact
0.81

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article

Diversity of BRAF mutations in non-small cell lung cancer and implications on treatment

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1 citations
npj Precision Oncology
Melanoma and MAPK Pathways
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article

Diversity of BRAF mutations in non-small cell lung cancer and implications on treatment

Ravi Salgia, John Paul Shen, Faisal Khurshid, Isa Mambetsariev, Fernando J. López-Díaz, Hatim Husain, Jeremy Fricke, Alessandro Leal, Aaron S. Mansfield, Antonious Hazim, Jonathan Wesley Riess, Kevin Lu, Kaushal Parikh, Vamsidhar Velcheti, Abhinav B Madduri, Brian Woodward
article en
1 citations

Abstract

The optimal treatment sequence in non-small cell lung cancer harboring class I BRAF mutations and atypical BRAF variants remains unclear. To better characterize therapeutic strategy, we retrospectively evaluated a multi-institutional cohort of BRAF-mutant NSCLC patients (n = 97) and an independent clinico-genomic database (n = 342), performed structural modeling, and conducted chemical screens of BRAF-mutant cell lines. Patients with class I BRAF mutation treated with BRAF-MEK inhibitors at any line of therapy had significantly greater median overall survival compared to those who did not receive BRAF-MEK inhibitors (40 vs 10 months, Log-rank p = 0.043). There, however, was no significant survival difference between patients treated with immune checkpoint inhibitors versus those not treated. Tumors with class II or III BRAF variants were significantly more likely to harbor concurrent MAPK pathway alterations relative to class I (Chi-Square p < 10<sup>-4</sup>). Cell line studies identified genetic dependency on BRAF in class II cell lines without sensitivity to BRAF inhibitors, and dependency on EGFR in class III cell lines.

npj Precision OncologyVol. 9(1)
The University of Texas MD Anderson Cancer Center (US), UC San Diego Health System (US), University of California San Diego (US), NYU Langone Health (US), City of Hope (US), Mayo Clinic in Arizona (US), Cordoba University (US), University of California, Davis (US)
Cancer Prevention and Research Institute of Texas
Openalex Percentile: Top 22%
Melanoma and MAPK Pathways
0.81
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