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

Author:

Cavagna Rodrigo de Oliveira1ORCID,Escremim de Paula Flávia2,Berardinelli Gustavo Noriz2,Bonatelli Murilo2ORCID,Santana Iara3,Albino da Silva Eduardo Caetano3,Teixeira Gustavo Ramos34ORCID,Zaniolo Beatriz Garbe14,Mourão Dias Josiane5ORCID,Ferreira da Silva Flávio Augusto5,Baston Silva Carlos Eduardo5ORCID,Guimarães Marcela Gondim Borges5,Barone Camila Pinto5,Jacinto Alexandre Arthur6ORCID,Noleto da Nóbrega Oliveira Rachid Eduardo7,Miziara José Elias7,De Marchi Pedro18ORCID,Molina-Vila Miguel A9ORCID,Leal Letícia Ferro14ORCID,Reis Rui Manuel121011ORCID

Affiliation:

1. Barretos Cancer Hospital Molecular Oncology Research Center, , Barretos, Brazil

2. Barretos Cancer Hospital Molecular Diagnostic Laboratory, , Barretos, Brazil

3. Barretos Cancer Hospital Department of Pathology, , Barretos, Brazil

4. Dr. Paulo Prata – FACISB Barretos School of Health Sciences, , Barretos, Brazil

5. Barretos Cancer Hospital Department of Medical Oncology, , Barretos, Brazil

6. Barretos Cancer Hospital Deparment of Radiation Therapy, , Barretos, Brazil

7. Barretos Cancer Hospital Deparment of Thoracic Surgery, , Barretos, Brazil

8. Oncoclinicas , Rio de Janeiro , Brazil

9. Dexeus University Hospital Laboratory of Oncology/Pangaea Oncology, , Barcelona, Spain

10. University of Minho Life and Health Sciences Research Institute (ICVS), School of Medicine, , Braga, Portugal

11. ICVS/3B’s—PT Government Associate Laboratory , Braga/Guimarães, Portugal

Abstract

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.

Publisher

Oxford University Press (OUP)

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