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Efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer harboring BRAF mutations

BACKGROUND: Despite immune checkpoint inhibitors (ICI) being widely used to treat patients with advanced non-small cell lung cancer (NSCLC), few studies examine the role of ICI in patients with proto-oncogene B-Raf, serine/threonine kinase (BRAF) mutations. METHODS: A retrospective study was conduct...

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Detalles Bibliográficos
Autores principales: Wang, Haowei, Cheng, Lei, Zhao, Chao, Zhou, Fei, Jiang, Tao, Guo, Haoyue, Shi, Jinpeng, Chen, Peixin, Tang, Zhuoran, Mao, Shiqi, Jia, Keyi, Ye, Lingyun, Cai, Chenlei, Li, Xuefei, Chen, Xiaoxia, Zhou, Caicun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989805/
https://www.ncbi.nlm.nih.gov/pubmed/36895926
http://dx.doi.org/10.21037/tlcr-22-613
Descripción
Sumario:BACKGROUND: Despite immune checkpoint inhibitors (ICI) being widely used to treat patients with advanced non-small cell lung cancer (NSCLC), few studies examine the role of ICI in patients with proto-oncogene B-Raf, serine/threonine kinase (BRAF) mutations. METHODS: A retrospective study was conducted for patients with BRAF-mutant NSCLC who received treatment at Shanghai Pulmonary Hospital between 2014 and 2022. Primary end point was progression-free survival (PFS). Secondary end point was best response (RECIST, version 1.1). RESULTS: The study involved a total of 34 patients with 54 treatments recorded. The median PFS for the whole cohort was 5.8 months and the overall objective response rate (ORR) was 24%. Patients who were treated with ICI combined with chemotherapy reported a median PFS of 12.6 months and an ORR of 44%. Those who were treated with non-ICI therapy came with a median PFS of 5.3 months and an ORR of 14%. Specifically, patients had better clinical benefits with first-line ICI-combined therapy. The PFS was 18.5 months whereas that of non-ICI group was 4.1 months. The ORR was 56% in ICI-combined group and 10% in non-ICI cohort. CONCLUSIONS: The findings observed an evidential and significant susceptibility to ICIs combined therapy in patients with BRAF-mutant NSCLC, especially in first-line treatment.