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Molecular profile of driver genes in lung adenocarcinomas of Brazilian patients who have never smoked: implications for targeted therapies.

Authors :
Cavagna, Rodrigo de Oliveira
Paula, Flávia Escremim de
Berardinelli, Gustavo Noriz
Bonatelli, Murilo
Santana, Iara
Silva, Eduardo Caetano Albino da
Teixeira, Gustavo Ramos
Zaniolo, Beatriz Garbe
Dias, Josiane Mourão
Silva, Flávio Augusto Ferreira da
Silva, Carlos Eduardo Baston
Guimarães, Marcela Gondim Borges
Barone, Camila Pinto
Jacinto, Alexandre Arthur
Oliveira, Rachid Eduardo Noleto da Nóbrega
Miziara, José Elias
Marchi, Pedro De
Molina-Vila, Miguel A
Leal, Letícia Ferro
Reis, Rui Manuel
Source :
Oncologist; Oct2024, Vol. 29 Issue 10, pe1419-e1424, 6p
Publication Year :
2024

Abstract

Introduction Lung cancer in never-smoker (LCINS) patients accounts for 20% of lung cancer cases, and its biology remains poorly understood, particularly in genetically admixed populations. We elucidated the molecular profile of driver genes in Brazilian LCINS. Methods The mutational and gene fusion status of 119 lung adenocarcinomas from self-reported never-smoker patients, was assessed using targeted sequencing (NGS), nCounter, and immunohistochemistry. A panel of 46 ancestry-informative markers determined patients' genetic ancestry. Results The most frequently mutated gene was EGFR (49.6%), followed by TP53 (39.5%), ALK (12.6%), ERBB2 (7.6%), KRAS (5.9%), PIK3CA (1.7%), and less than 1% alterations in RET , NTRK1 , MET ∆ex14, PDGFRA , and BRAF. Except for TP53 and PIK3CA , all other alterations were mutually exclusive. Genetic ancestry analysis revealed a predominance of European (71.1%), and a higher African ancestry was associated with TP53 mutations. Conclusion Brazilian LCINS exhibited a similar molecular profile to other populations, except the increased ALK and TP53 alterations. Importantly, 73% of these patients have actionable alterations that are suitable for targeted treatments. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10837159
Volume :
29
Issue :
10
Database :
Complementary Index
Journal :
Oncologist
Publication Type :
Academic Journal
Accession number :
180152663
Full Text :
https://doi.org/10.1093/oncolo/oyae129