TY - JOUR
T1 - Mechanisms of Resistance to First-Line Osimertinib in Hispanic Patients With EGFR Mutant Non-Small Cell Lung Cancer (FRESTON-CLICaP)
AU - Cardona, Andrés F.
AU - Ruiz-Patiño, Alejandro
AU - Recondo, Gonzalo
AU - Martín, Claudio
AU - Raez, Luis
AU - Samtani, Suraj
AU - Minata, José Nicolas
AU - Blaquier, Juan Bautista
AU - Enrico, Diego
AU - Burotto, Mauricio
AU - Ordóñez-Reyes, Camila
AU - Chamorro, Diego F.
AU - Garcia-Robledo, Juan Esteban
AU - Corrales, Luis
AU - Zatarain-Barrón, Zyanya Lucia
AU - Más, Luis
AU - Sotelo, Carolina
AU - Ricaurte, Luisa
AU - Santoyo, Nicolas
AU - Cuello, Mauricio
AU - Mejía, Sergio
AU - Jaller, Elvira
AU - Vargas, Carlos
AU - Carranza, Hernán
AU - Otero, Jorge
AU - Rodríguez, July
AU - Archila, Pilar
AU - Bermudez, Maritza
AU - Gamez, Tatiana
AU - Cordeiro de Lima, Vladmir
AU - Freitas, Helano
AU - Russo, Alessandro
AU - Polo, Carolina
AU - Malapelle, Umberto
AU - Perez, Diego de Miguel
AU - Rolfo, Christian
AU - Viola, Lucia
AU - Rosell, Rafael
AU - Arrieta, Oscar
N1 - Publisher Copyright:
© 2022
PY - 2022/9
Y1 - 2022/9
N2 - 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.
AB - 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.
KW - Carcinoma
KW - Drug resistance
KW - EGFR mutations
KW - Non-Small-Cell Lung Cancer
KW - Osimertinib
UR - http://www.scopus.com/inward/record.url?scp=85133607813&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2022.06.001
DO - 10.1016/j.cllc.2022.06.001
M3 - Article
AN - SCOPUS:85133607813
SN - 1525-7304
VL - 23
SP - 522
EP - 531
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 6
ER -