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Mechanisms of Resistance to First-Line Osimertinib in Hispanic Patients With EGFR Mutant Non-Small Cell Lung Cancer (FRESTON-CLICaP).
Cardona, Andrés F; Ruiz-Patiño, Alejandro; Recondo, Gonzalo; Martín, Claudio; Raez, Luis; Samtani, Suraj; Minata, José Nicolas; Blaquier, Juan Bautista; Enrico, Diego; Burotto, Mauricio; Ordóñez-Reyes, Camila; Chamorro, Diego F; Garcia-Robledo, Juan Esteban; Corrales, Luis; Zatarain-Barrón, Zyanya Lucia; Más, Luis; Sotelo, Carolina; Ricaurte, Luisa; Santoyo, Nicolas; Cuello, Mauricio; Mejía, Sergio; Jaller, Elvira; Vargas, Carlos; Carranza, Hernán; Otero, Jorge; Rodríguez, July; Archila, Pilar; Bermudez, Maritza; Gamez, Tatiana; Cordeiro de Lima, Vladmir; Freitas, Helano; Russo, Alessandro; Polo, Carolina; Malapelle, Umberto; Perez, Diego de Miguel; Rolfo, Christian; Viola, Lucia; Rosell, Rafael; Arrieta, Oscar.
Afiliação
  • Cardona AF; Direction of Research and Education, Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center (CTIC), Bogotá, Colombia; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bo
  • Ruiz-Patiño A; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Recondo G; Thoracic Oncology Section, Centro de Educación Médica e Investigaciones Clínicas - CEMIC, Buenos Aires, Argentina.
  • Martín C; Medical Oncology Department, Thoracic Oncology Section, Instituto Alexander Fleming, Buenos Aires, Argentina.
  • Raez L; Thoracic Oncology Department, Memorial Cancer Institute, Memorial Health Care System, Miami, FL.
  • Samtani S; Medical Oncology Department, Bradford Hill Clinical Research Center, Santiago, Chile.
  • Minata JN; Medical Oncology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
  • Blaquier JB; Medical Oncology Department, Centro de Educación Médica e Investigaciones Clínicas - CEMIC, Buenos Aires, Argentina.
  • Enrico D; Medical Oncology Department, Thoracic Oncology Section, Instituto Alexander Fleming, Buenos Aires, Argentina.
  • Burotto M; Medical Oncology Department, Bradfordhill Institute, Santiago, Chile.
  • Ordóñez-Reyes C; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Chamorro DF; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Garcia-Robledo JE; Division of Hematology/Oncology, Mayo Clinic, Phoenix, AZ.
  • Corrales L; Clinical Oncology Department, Oncology Unit, Hospital San Juan de Dios/Centro de Investigación y Manejo del Cáncer (CIMCA), San José, Costa Rica.
  • Zatarain-Barrón ZL; Thoracic Oncology Unit, Instituto Nacional de Cancerología, México City México.
  • Más L; Medical Oncology Department, Instituto Nacional de Enfermedades Neoplásicas - INEN, Lima, Perú.
  • Sotelo C; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Ricaurte L; Pathology Department, Mayo Clinic, Rochester, MN.
  • Santoyo N; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Cuello M; Clinical Oncology Department, Hospital de Clinicas, Universidad de la Republica - UdeLAR, Montevideo, Uruguay.
  • Mejía S; Cancer Institute, Las Americas Clinic, Medellin, Colombia.
  • Jaller E; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Vargas C; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia; Clinical Oncology Department, Clínica del Country, Bogotá, Colombia.
  • Carranza H; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia; Clinical Oncology Department, Clínica del Country, Bogotá, Colombia.
  • Otero J; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia; Clinical Oncology Department, Clínica del Country, Bogotá, Colombia.
  • Rodríguez J; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Archila P; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Bermudez M; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Gamez T; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.
  • Cordeiro de Lima V; Medical Oncology Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Freitas H; Medical Oncology Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Russo A; Medical Oncology Unit, A.O. Papardo, Messina, Italy.
  • Polo C; Clinical Oncology Department, Instituto Nacional de Cancerología - INC, Bogotá, Colombia.
  • Malapelle U; Department of Public Health, University Federico II, Naples, Italy.
  • Perez DM; Center for Thoracic Oncology, The Tisch Cancer Institute Icahn School of Medicine, Mount Sinai, Mount Sinai Health System, One Gustave Levy Place, NY.
  • Rolfo C; Center for Thoracic Oncology, The Tisch Cancer Institute Icahn School of Medicine, Mount Sinai, Mount Sinai Health System, One Gustave Levy Place, NY.
  • Viola L; Thoracic Oncology Unit, Fundación Neumológica Colombiana, Bogotá, Colombia.
  • Rosell R; Cancer Biology and Precision Medicine Program, Catalan Institute of Oncology, Barcelona, Spain.
  • Arrieta O; Thoracic Oncology Unit, Instituto Nacional de Cancerología, México City México.
Clin Lung Cancer ; 23(6): 522-531, 2022 09.
Article em En | MEDLINE | ID: mdl-35798634
ABSTRACT

INTRODUCTION:

Osimertinib is a third generation EGFR-TKI inhibitor approved in the first-line setting for patients with advanced non-small cell lung cancer (NSCLC). Additionally, it represents the treatment of choice in patients who present with T790M mutations and evidence of relapse of the disease. Effectiveness and safety of this drug have been studied in multiple clinical trials and observational studies, however, information regarding outcomes among Hispanic patients treated with Osimertinib is scarce. The objective of this study was to examine real-world effectiveness and safety of first-line Osimertinib in a cohort of Hispanic patients with NSCLC, emphasizing post-progression outcomes.

METHODS:

This is a multicenter, multinational, retrospective cohort study of Hispanic patients treated with Osimertinib as first-line for EGFR-mutated NSCLC. Patients with a confirmed diagnosis of metastatic EGFR-mutated NSCLC who received Osimertinib (80mg/day until evidence of disease progression or presence of intolerable adverse effects) were identified and included. NGS was performed in tumor samples or liquid biopsies among patients who had disease progression. The primary outcome was progression-free survival, and the secondary outcome was post-progression survival.

RESULTS:

A total of 94 patients from Mexico, Argentina, Costa Rica, Colombia, Panama, Chile and the USA were included, with a median age of 59 years. Identified mutations included EGFR Exon 19 deletions and EGFR pL858R point mutations. Median progression-free survival (PFS) was 14.4 months (95%CI 12.4-18.2 months). Lung/pleura and lymph nodes were the most common sites of progression. Median post-progression survival was 7.73 months (95%CI 4.07 months-Not reached). Factors which negatively affected PFS included presence of liver metastases at diagnosis and a tumor mutational burden > 5 mut/Mb.

CONCLUSION:

Treatment with first line osimertinib represents an effective and safe option for Hispanic patients with metastatic NSCLC. Liver metastases and a higher tumor mutation burden were associated with a lower PFS. Despite effectiveness, different mechanisms of resistance were identified among the patients in this cohort, including mutations which can be targeted by other therapeutic options.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Resistencia a Medicamentos Antineoplásicos / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: Clin Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Resistencia a Medicamentos Antineoplásicos / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: Clin Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article