Actionable mutations in non-small cell lung cancer in patients at hospital de Especialidades Eugenio Espejo, Ecuador 2017–2020
-
Miguel Ángel Fernández Freire
, Gabriela Isabel Gálvez Salazar
, Mariana Meira Scudeler
, Fernanda Rodrigues-Soares
, Gabriela Fernanda Jaramillo Koupermann
and Andrea Paola Moreno Ocampo
Abstract
Objectives
Determine the frequency of actionable mutations in non-small cell lung cancer (NSCLC) and their correlation with overall survival (OS) and the site of metastases.
Methods
We performed a descriptive cross-sectional study at the Hospital de Especialidades Eugenio Espejo, Ecuador, between 2017 and 2020. Demographic, pathological, and molecular alterations in epidermal growth factor (EGFR), Anaplastic lymphoma kinase (ALK), ROS proto-oncogene 1 (ROS1), Programmed death-ligand 1 (PD-L1) expression, and clinical data detailed in patients’ medical records with metastatic NSCLC were collected and analyzed.
Seventy-nine stage IV patients had NSCLC; adenocarcinoma histology represents 56 (70.9%). The predominant mutation was in EGFR (22.8%); the most common variant was the deletion of exon 19 (72.2%). The most common metastatic site was in the contralateral lung (22.3%); however, this variable showed no significant correlation to the molecular markers (p=0.057). The overall survival (OS) and the status of molecular markers are not statistically significant (p=0.27). OS was better for non-mutated EGFR than for mutated EGFR (p=0.012). However, the frequency values are unrelated to contralateral lung metastasis or survival.
Conclusions
Our frequency mutations are concordant with those found in other studies in Latin America. EGFR was the most common biomarker mutation, and there was a better OS in EGFR non-mutated patient.
-
Research funding: None declared.
-
Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
-
Competing interests: Authors state no conflict of interest.
-
Informed consent: Informed consent was obtained from all individuals included in this study.
-
Ethical approval: The Institutional Review Board approval was obtained through the investigation department at the Hospital de Especialidades Eugenio Espejo Quito – Ecuador.
References
1. Globocan. Lung Source: Globocan 2020. International Agency for Research on Cancer (IARC); 2020, 419:7–8 pp. https://gco.iarc.fr/today/data/factsheets/cancers/15-Lung-fact-sheet.pdf [Accessed 2021 Oct 23]. In press.Search in Google Scholar
2. Globocan. Ecuador Source: Globocan 2020. International Agency for Reserch on Cancer; 2020, 563:1–2 pp. https://gco.iarc.fr/today/data/factsheets/populations/218-ecuador-fact-sheets.pdf. In press.Search in Google Scholar
3. Travis, WD, Brambilla, E, Nicholson, AG, Yatabe, Y, Austin, JHM, Beasley, MB, et al.. The 2015 World health organization classification of lung tumors: impact of genetic, clinical and radiologic advances since the 2004 classification. J Thorac Oncol 2015;10:1243–60. https://doi.org/10.1097/jto.0000000000000630.Search in Google Scholar
4. Hirsch, FR, Scagliotti, GV, Mulshine, JL, Kwon, R, Curran, WJ, Wu, YL, et al.. Lung cancer: current therapies and new targeted treatments. Lancet 2017;389:299–311. https://doi.org/10.1016/s0140-6736(16)30958-8.Search in Google Scholar PubMed
5. NCCN. Non-Small Cell Lung Cancer V.4.2020 – Follow-up – May 11, 2020. Avaliable from: https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&cad=rja&uact=8&ved=2ahUKEwiTooz-8p__AhWIUXcKHRj9A3sQFnoECB8QAQ&url=https%3A%2F%2Fwww.nccn.org%2Fguidelines%2Fguidelines-process%2Ftransparency-process-and-recommendations%2FGetFileFromFileManagerGuid%3FFileManagerGuidId%3D241ff566-37b1-4d8b-9c4b-cc8230b883e4&usg=AOvVaw0_LzIlV7x6tVbnCoSvYCRy. [Accessed 11 May 2020].Search in Google Scholar
6. Marino, FZ, Bianco, R, Marina Accardo, M, Ronchi, A, Cozzolino, I, Morgillo, F, et al.. Molecular heterogeneity in lung cancer: from mechanisms of origin to clinical implications. Int J Med Sci 16;2019;:981–9. https://doi.org/10.1200/edbk_237863.Search in Google Scholar
7. Wadowska, K, Bil-Lula, I, Trembecki, Ł, Śliwińska-Mossoń, M. Genetic markers in lung cancer diagnosis: a review. Int J Mol Sci 2020;21:4569.10.3390/ijms21134569Search in Google Scholar PubMed PubMed Central
8. Roche cobas. cobas ® EGFR mutation test v2 for in vitro diagnostic use. Mannheim, Germany: Roche Molecular Systems; 2016:1–71 pp.Search in Google Scholar
9. Roche Ventana. VENTANA anti-ALK (D5F3) rabbit monoclonal primary Antibody. Mannheim, Germany: Roche Molecular Systems; 2015:1–4 pp.Search in Google Scholar
10. Roche Ventana. VENTANA ROS-1 (SP384) rabbit monoclonal primary antibody. Mannheim, Germany: Roche Molecular Systems; 2019, 790–6087:1–4 pp.Search in Google Scholar
11. Roche Ventana. VENTANA PD-L1 (SP263) assay. Mannheim, Germany: Ventana Medical Systems; 2018, 1.Search in Google Scholar
12. De Oliveira, ACDSM, Da Silva, AVA, Alves, M, Cronemberger, E, Carneiro, BA, Melo, JC, et al.. Molecular profile of non-small cell lung cancer in northeastern Brazil. J Bras Pneumol 2019;45:1–7. https://doi.org/10.1590/1806-3713/e20180181.Search in Google Scholar PubMed PubMed Central
13. Arrieta, O, Cardona, AF, Federico Bramuglia, G, Gallo, A, Campos-Parra, AD, Serrano, S, et al.. Genotyping non-small cell lung cancer (NSCLC) in Latin America. J Thorac Oncol 2011;6:1955–9. https://doi.org/10.1097/jto.0b013e31822f655f.Search in Google Scholar PubMed
14. Arrieta, O, Cardona, AF, Martín, C, Más-López, L, Corrales-Rodríguez, L, Bramuglia, G, et al.. Updated frequency of EGFR and KRAS mutations in NonSmall-cell lung cancer in Latin America: the Latin-American consortium for the investigation of lung cancer (CLICaP). J Thorac Oncol 2015;10:838–43. https://doi.org/10.1097/jto.0000000000000481.Search in Google Scholar
15. Rivas, C, Luis Martinez, EET. Prevalence of epidermal growth factor receptor (EGFR) mutation in an Ecuadorian population with non-small cell lung cancer (NSCLC). J Clin Oncol 2014;15:e19157–e19157. https://doi.org/10.1200/jco.2014.32.15_suppl.e19157.Search in Google Scholar
16. Aguiar, F, Fernandes, G, Queiroga, H, Machado, JC, Cirnes, L, Souto Moura, C, et al.. Overall survival analysis and characterization of an EGFR mutated non-small cell lung cancer (NSCLC) population. Arch Bronconeumol 2018;54:10–7. https://doi.org/10.1016/j.arbres.2017.07.012.Search in Google Scholar PubMed
17. Beypinar, I, Demir, H, Araz, M, Uysal, M. The relationship between EGFR mutation and metastasis pattern in lung adenocarcinoma. J oncol sci 2019;5:65–9. https://doi.org/10.1016/j.jons.2019.08.002.Search in Google Scholar
© 2022 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Editorial
- Pharmacogenetics and ethnicity: “Dr. José María Cantú” award announcement
- Review
- A review of pharmacogenetic studies in the Bangladeshi population
- Original Articles
- The ANKK1/DRD2 gene TaqIA polymorphism (rs1800497) is associated with the severity of extrapyramidal side effects of haloperidol treatment in CYP2D6 extensive metabolizers with schizophrenia spectrum disorders
- Effect of CYP2D6*4, CYP2D6*10 polymorphisms on the safety of treatment with timolol maleate in patients with glaucoma
- Actionable mutations in non-small cell lung cancer in patients at hospital de Especialidades Eugenio Espejo, Ecuador 2017–2020
- Impact of FCGR2A R131H, FCGR3A F158V and FCGR3B NA1/NA2 polymorphisms on response to Fc-containing TNF inhibitors in Tunisian rheumatoid arthritis patients
- CYP2C9 gene polymorphisms influence on antihypertensive effectiveness and hypouricemic effect of losartan among patients with arterial hypertension: an observational study
- Assessing the efficacy and safety of Unani pharmacopoeial formulations in dermatophytosis (quba) – a randomized controlled trial
- Quantitative assessment of antioxidant potential of selected homeopathic preparations in clinical practice
- Influence of EPHX1 c.337 T>C and UGT2B7*2 genetic polymorphisms on the requirement of carbamazepine maintenance dose in persons with epilepsy (PWE) of Southern part of India: a cross-sectional genetic association study
- Cathine and cathinone disposition kinetics and neurotransmitter profile in several organs of rats exposed to a single dose of Catha edulis (Vahl) Forssk. ex Endl. extract
Articles in the same Issue
- Frontmatter
- Editorial
- Pharmacogenetics and ethnicity: “Dr. José María Cantú” award announcement
- Review
- A review of pharmacogenetic studies in the Bangladeshi population
- Original Articles
- The ANKK1/DRD2 gene TaqIA polymorphism (rs1800497) is associated with the severity of extrapyramidal side effects of haloperidol treatment in CYP2D6 extensive metabolizers with schizophrenia spectrum disorders
- Effect of CYP2D6*4, CYP2D6*10 polymorphisms on the safety of treatment with timolol maleate in patients with glaucoma
- Actionable mutations in non-small cell lung cancer in patients at hospital de Especialidades Eugenio Espejo, Ecuador 2017–2020
- Impact of FCGR2A R131H, FCGR3A F158V and FCGR3B NA1/NA2 polymorphisms on response to Fc-containing TNF inhibitors in Tunisian rheumatoid arthritis patients
- CYP2C9 gene polymorphisms influence on antihypertensive effectiveness and hypouricemic effect of losartan among patients with arterial hypertension: an observational study
- Assessing the efficacy and safety of Unani pharmacopoeial formulations in dermatophytosis (quba) – a randomized controlled trial
- Quantitative assessment of antioxidant potential of selected homeopathic preparations in clinical practice
- Influence of EPHX1 c.337 T>C and UGT2B7*2 genetic polymorphisms on the requirement of carbamazepine maintenance dose in persons with epilepsy (PWE) of Southern part of India: a cross-sectional genetic association study
- Cathine and cathinone disposition kinetics and neurotransmitter profile in several organs of rats exposed to a single dose of Catha edulis (Vahl) Forssk. ex Endl. extract