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Genomic analysis and clinical correlations of non-small cell lung cancer brain metastasis

Up to 50% of patients with non-small cell lung cancer (NSCLC) develop brain metastasis (BM), yet the study of BM genomics has been limited by tissue access, incomplete clinical data, and a lack of comparison with paired extracranial specimens. Here we report a cohort of 233 patients with resected an...

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Detalles Bibliográficos
Autores principales: Skakodub, Anna, Walch, Henry, Tringale, Kathryn R., Eichholz, Jordan, Imber, Brandon S., Vasudevan, Harish N., Li, Bob T., Moss, Nelson S., Hei Yu, Kenny Kwok, Mueller, Boris A., Powell, Simon, Razavi, Pedram, Yu, Helena A., Reis-Filho, Jorge S., Gomez, Daniel, Schultz, Nikolaus, Pike, Luke R. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10435547/
https://www.ncbi.nlm.nih.gov/pubmed/37591896
http://dx.doi.org/10.1038/s41467-023-40793-x
Descripción
Sumario:Up to 50% of patients with non-small cell lung cancer (NSCLC) develop brain metastasis (BM), yet the study of BM genomics has been limited by tissue access, incomplete clinical data, and a lack of comparison with paired extracranial specimens. Here we report a cohort of 233 patients with resected and sequenced (MSK-IMPACT) NSCLC BM and comprehensive clinical data. With matched samples (47 primary tumor, 42 extracranial metastatic), we show CDKN2A/B deletions and cell cycle pathway alterations to be enriched in the BM samples. Meaningful clinico-genomic correlations are noted, namely EGFR alterations in leptomeningeal disease (LMD) and MYC amplifications in multifocal regional brain progression. Patients who developed early LMD frequently have had uncommon, multiple, and persistently detectable EGFR driver mutations. The distinct mutational patterns identified in BM specimens compared to other tissue sites suggest specific biologic underpinnings of intracranial progression.