Lazertinib Versus Gefitinib Tyrosine Kinase Inhibitors in Treatment-Naíve Patients With EGFR-Mutated Advanced NSCLC: Analysis of the Asian Subpopulation in LASER301
Issued Date
2023-10-01
Resource Type
ISSN
15560864
eISSN
15561380
Scopus ID
2-s2.0-85171987980
Pubmed ID
37702629
Journal Title
Journal of Thoracic Oncology
Volume
18
Issue
10
Start Page
1351
End Page
1361
Rights Holder(s)
SCOPUS
Bibliographic Citation
Journal of Thoracic Oncology Vol.18 No.10 (2023) , 1351-1361
Suggested Citation
Reungwetwattana T., Cho B.C., Lee K.H., Pang Y.K., Fong C.H., Kang J.H., Lee Y.G., Lim C.S., Danchaivijitr P., Lim Y.N., Lee Y., How S.H., Geater S., Lee S.S., Min Y.J., Kim J.H., Lee J.S., Lee G.W., Soo R.A., Lee S.Y., Choi S.Y., Ahn M.J. Lazertinib Versus Gefitinib Tyrosine Kinase Inhibitors in Treatment-Naíve Patients With EGFR-Mutated Advanced NSCLC: Analysis of the Asian Subpopulation in LASER301. Journal of Thoracic Oncology Vol.18 No.10 (2023) , 1351-1361. 1361. doi:10.1016/j.jtho.2023.06.016 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/90299
Title
Lazertinib Versus Gefitinib Tyrosine Kinase Inhibitors in Treatment-Naíve Patients With EGFR-Mutated Advanced NSCLC: Analysis of the Asian Subpopulation in LASER301
Author's Affiliation
The Catholic University of Korea Seoul St. Mary's Hospital
Ulsan University Hospital
Siriraj Hospital
Yonsei Cancer Hospital
Chungbuk National University Hospital
Hospital Pulau Pinang
Seoul National University Bundang Hospital
Hospital Umum Sarawak
Yuhan Corporation
National Cancer Center, Gyeonggi
Inje University, College of Medicine
Samsung Medical Center, Sungkyunkwan university
SKKU School of Medicine
Faculty of Medicine Ramathibodi Hospital, Mahidol University
University of Malaya Medical Centre
Gyeongsang National University (GSNU), College of Medicine
Prince of Songkla University
College of Medicine, Pochon CHA University
National University Cancer Institute
Hospital Tengku Ampuan Afzan
Hospital Sultan Ismail
Ulsan University Hospital
Siriraj Hospital
Yonsei Cancer Hospital
Chungbuk National University Hospital
Hospital Pulau Pinang
Seoul National University Bundang Hospital
Hospital Umum Sarawak
Yuhan Corporation
National Cancer Center, Gyeonggi
Inje University, College of Medicine
Samsung Medical Center, Sungkyunkwan university
SKKU School of Medicine
Faculty of Medicine Ramathibodi Hospital, Mahidol University
University of Malaya Medical Centre
Gyeongsang National University (GSNU), College of Medicine
Prince of Songkla University
College of Medicine, Pochon CHA University
National University Cancer Institute
Hospital Tengku Ampuan Afzan
Hospital Sultan Ismail
Other Contributor(s)
Abstract
Introduction: Lazertinib is a third-generation central nervous system–penetrant tyrosine kinase inhibitor targeting mutant EGFR in NSCLC. Lazertinib exhibited improved efficacy versus gefitinib in the LASER301 study; this subset analysis compared lazertinib with gefitinib among Asian patients. Methods: The phase 3 LASER301 study evaluated lazertinib efficacy and safety in treatment-naive patients with EGFR-mutated (exon 19 deletion or L858R) locally advanced or metastatic NSCLC. Patients were randomized one-to-one and received either lazertinib or gefitinib. The primary end point was investigator-assessed progression-free survival using Response Evaluation Criteria in Solid Tumors version 1.1. Secondary end points included overall survival, objective response rate, duration of response, and safety. Results: Between February 13, 2020, and July 29, 2022, among 258 patients of Asian descent, the median progression-free survival was significantly longer with lazertinib than gefitinib (20.6 versus 9.7 mo; hazard ratio: 0.46; 95% confidence interval [CI]: 0.34–0.63, p < 0.001), and the benefit was consistent across predefined subgroups (exon 19 deletion, L858R, baseline central nervous system metastases). Objective response rate and disease control rates were similar between treatment groups. The median duration of response was 19.4 months (95% CI: 16.6–24.9) versus 9.6 months (95% CI: 6.9–12.4) in the lazertinib versus gefitinib group. Adverse event rates in Asian patients were comparable with the overall LASER301 population. Adverse events leading to discontinuation in the lazertinib and gefitinib groups were 13% and 12%, respectively. Conclusions: In LASER301, efficacy and safety results in Asian patients were consistent with the overall population. Lazertinib exhibited better efficacy than gefitinib in Asian patients with a tolerable safety profile.