Final Report on Real-World Effectiveness of Sequential Afatinib and Osimertinib in EGFR Positive Advanced Non-Small Cell Lung Cancer: Updated Analysis of the RESET Study
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Purpose This study aimed to report the final analysis of time-on-treatment (TOT) and overall survival (OS) in patients with advanced-stage epidermal growth factor receptor (EGFR)+ non–small cell lung cancer (NSCLC) who received sequential afatinib and osimertinib and to compare the outcomes with other second-line regimens (comparator group). Materials and Methods In this updated report, the existing medical records were reviewed and rechecked. TOT and OS were updated and analyzed according to clinical features using the Kaplan-Meier method and log-rank test. TOT and OS were compared with those of the comparator group, in which most patients received pemetrexed-based treatments. A multivariable Cox proportional hazard model was used to evaluate features that could affect survival outcomes. Results The median observation time was 31.0 months. The follow-up period was extended to 20 months. A total of 401 patients who received first-line afatinib were analyzed (166 with T790M+ and second-line osimertinib, and 235 with unproven T790M and other second-line agents). Median TOTs on afatinib and osimertinib were 15.0 months (95% confidence interval [CI], 14.0 to 16.1) and 11.9 months (95% CI, 8.9 to 14.6), respectively. The median OS in the osimertinib group was 54.3 months (95% CI, 46.7 to 61.9), much longer than that in the comparator group. In patients who received osimertinib, the OS was longest with Del19+ (median, 59.1; 95% CI, 48.7 to 69.5). Conclusion This is one of the largest real-world studies reporting the encouraging activity of sequential afatinib and osimertinib in Asian patients with EGFR+ NSCLC who acquired the T790M mutation, particularly Del19+.
Abstract
Purpose This study aimed to report the final analysis of time-on-treatment (TOT) and overall survival (OS) in patients with advanced-stage epidermal growth factor receptor (EGFR)+ non–small cell lung cancer (NSCLC) who received sequential afatinib and osimertinib and to compare the outcomes with other second-line regimens (comparator group). Materials and Methods In this updated report, the existing medical records were reviewed and rechecked. TOT and OS were updated and analyzed according to clinical features using the Kaplan-Meier method and log-rank test. TOT and OS were compared with those of the comparator group, in which most patients received pemetrexed-based treatments. A multivariable Cox proportional hazard model was used to evaluate features that could affect survival outcomes. Results The median observation time was 31.0 months. The follow-up period was extended to 20 months. A total of 401 patients who received first-line afatinib were analyzed (166 with T790M+ and second-line osimertinib, and 235 with unproven T790M and other second-line agents). Median TOTs on afatinib and osimertinib were 15.0 months (95% confidence interval [CI], 14.0 to 16.1) and 11.9 months (95% CI, 8.9 to 14.6), respectively. The median OS in the osimertinib group was 54.3 months (95% CI, 46.7 to 61.9), much longer than that in the comparator group. In patients who received osimertinib, the OS was longest with Del19+ (median, 59.1; 95% CI, 48.7 to 69.5). Conclusion This is one of the largest real-world studies reporting the encouraging activity of sequential afatinib and osimertinib in Asian patients with EGFR+ NSCLC who acquired the T790M mutation, particularly Del19+.
참고문헌 (24)
- Ferlay J, "Cancer statistics for the year 2020 : an overview", Int J Cancer, 149, pp.778~789 (2021)
- Zhang Y, "Global patterns and trends in lung cancer incidence : a population-based study", J Thorac Oncol, 16, pp.933~944 (2021)
- Cheng TY, "The international epidemiology of lung cancer : latest trends, disparities, and tumor characteristics", J Thorac Oncol, 11, pp.1653~1671 (2016)
- Lortet-Tieulent J, "International trends in lung cancer incidence by histological subtype : adenocarcinoma stabilizing in men but still increasing in women", Lung Cancer, 84, pp.13~22 (2014)
- Lee Jae Guk, "Recent Trends of Lung Cancer in Korea", Tuberculosis and Respiratory Diseases, 84(2), pp.89~95 (2021), 대한결핵및호흡기학회[DOI]
- Soria JC, "Osimertinib in untreated EGFR-mutated advanced non-small-cell lung cancer", N Engl J Med, 378, pp.113~125 (2018)
- Ke EE, "A higher proportion of the EGFR T790M mutation may contribute to the better survival of patients with exon 19 deletions compared with those with L858R", J Thorac Oncol, 12, pp.1368~1375 (2017)
- Mok TS, "Osimertinib or platinum-pemetrexed in EGFR T790M-positive lung cancer", N Engl J Med, 376, pp.629~640 (2017)
- Paz-Ares L, "Afatinib versus gefitinib in patients with EGFR mutation-positive advanced non-small-cell lung cancer : overall survival data from the phase IIb LUX-Lung 7 trial", Ann Oncol, 28, pp.270~277 (2017)
- Hochmair MJ, "Sequential afatinib and osimertinib in patients with EGFR mutation-positive non-small-cell lung cancer : final analysis of the GioTag study", Future Oncol, 16, pp.2799~2808 (2020)
- Popat S, "Sequential afatinib and osimertinib in patients with EGFR mutation-positive NSCLC and acquired T790M : a global non-interventional study(UpSwinG)", Lung Cancer, 162, pp.9~15 (2021)
- Kim T, "Sequential treatment of afatinib and osimertinib or other regimens in patients with advanced non-small-cell lung cancer harboring EGFR mutations : results from a real-world study in South Korea", Cancer Med, 10, pp.5809~5822 (2021)
- Wu YL, "Afatinib versus cisplatin plus gemcitabine for first-line treatment of Asian patients with advanced non-small-cell lung cancer harbouring EGFR mutations(LUX-Lung 6) : an open-label, randomised phase 3 trial", Lancet Oncol, 15, pp.213~222 (2014)
- Akamatsu H, "Osimertinib in Japanese patients with EGFR T790M mutation-positive advanced non-small-cell lung cancer : AURA3 trial", Cancer Sci, 109, pp.1930~1938 (2018)
- Smit EF, "Randomized phase II and pharmacogenetic study of pemetrexed compared with pemetrexed plus carboplatin in pretreated patients with advanced non-small-cell lung cancer", J Clin Oncol, 27, pp.2038~2045 (2009)
- Miura S, "Sequential afatinib and osimertinib in Asian patients with EGFR mutation-positive non-dmall vell lung cancer and acquired T790M : combined analysis of two global non-interventional studies", Onco Targets Ther, 15, pp.873~882 (2022)
- Kogure Y, "T790M correlates with longer progression-free survival in non-small cell lung carcinomas harboring EGFR mutations", In Vivo, 32, pp.1199~1204 (2018)
- Gaut D, "Clinical implications of the T790M mutation in disease characteristics and treatment response in patients with epidermal growth factor receptor(EGFR)-mutated non-small-cell lung cancer(NSCLC)", Clin Lung Cancer, 19, pp.e19~28 (2018)
- Chmielecki J, "Optimization of dosing for EGFR-mutant non-small cell lung cancer with evolutionary cancer modeling", Sci Transl Med, 3, pp.90ra59~ (2011)
- Regales L, "Development of new mouse lung tumor models expressing EGFR T790M mutants associated with clinical resistance to kinase inhibitors", PLoS One, 2, pp.e810~ (2007)
- Leonetti A, "Resistance mechanisms to osimertinib in EGFR-mutated non-small cell lung cancer", Br J Cancer, 121, pp.725~737 (2019)
- Yonesaka K, "Dual blockade of EGFR tyrosine kinase using osimertinib and afatinib eradicates EGFR‑mutant Ba", F3 cells, 2019, pp.41, 1059~1066
- Ramalingam SS, "Overall survival with osimertinib in untreated, EGFR-mutated advanced NSCLC", N Engl J Med, 382, pp.41~50 (2020)
- 강미주, "Cancer Statistics in Korea: Incidence, Mortality, Survival, and Prevalence in 2019", Cancer Research and Treatment, 54(2), pp.330~344 (2022), 대한암학회[DOI]
