Immune biomarkers and response to checkpoint inhibition of BRAFV600 and BRAF non-V600 altered lung cancers

• Published in: British journal of cancer Vol. 126; no. 6; pp. 889 - 898
• Main Authors: Murciano-Goroff, Yonina R., Pak, Terry, Mondaca, Sebastian, Flynn, Jessica R., Montecalvo, Joseph, Rekhtman, Natasha, Halpenny, Darragh, Plodkowski, Andrew J., Wu, Stephanie L., Kris, Mark G., Paik, Paul K., Riely, Gregory J., Yu, Helena A., Rudin, Charles M., Hellmann, Matthew D., Land, Josiah D., Buie, Larry W., Heller, Glenn, Lito, Piro, Yaeger, Rona, Drilon, Alexander, Liu, Dazhi, Li, Bob T., Offin, Michael
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.04.2022; Nature Publishing Group
• Subjects: 631/67/1612; 631/67/322; Biomedical and Life Sciences; Biomedicine; Cancer Research; Disease control; Drug Resistance; Epidemiology; Immune checkpoint inhibitors; Lung cancer; Lung diseases; Metastases; Molecular Medicine; Mutation; Next-generation sequencing; Oncology; Patients; Tumors
• ISSN: 0007-0920; 1532-1827; 1532-1827
• DOI: 10.1038/s41416-021-01679-1

Background While 2–4% of lung cancers possess alterations in BRAF , little is known about the immune responsiveness of these tumours. Methods Clinical and genomic data were collected from 5945 patients with lung cancers whose tumours underwent next-generation sequencing between 2015 and 2018. Patients were followed through 2020. Results In total, 127 patients with metastatic BRAF -altered lung cancers were identified: 29 tumours had Class I mutations, 59 had Class II/III alterations, and 39 had variants of unknown significance (VUS). Tumour mutation burden was higher in Class II/III than Class I-altered tumours (8.8 mutations/Mb versus 4.9, P  < 0.001), but this difference was diminished when stratified by smoking status. The overall response rate to immune checkpoint inhibitors (ICI) was 9% in Class I-altered tumours and 26% in Class II/III ( P  = 0.25), with median time on treatment of 1.9 months in both groups. Among patients with Class I–III-altered tumours, 36-month HR for death in those who ever versus never received ICI was 1.82 (1.17–6.11). Nine patients were on ICI for >2 years (two with Class I mutations, two with Class II/III alterations, and five with VUS). Conclusions A subset of patients with BRAF -altered lung cancers achieved durable disease control on ICI. However, collectively no significant clinical benefit was seen.