1 2

Cited 0 times in

Cited 0 times in

Lazertinib Versus Osimertinib in Previously Untreated EGFR-Mutant Advanced NSCLC: A Randomized, Double-Blind, Exploratory Analysis From MARIPOSA

Authors
 Lee, Se-Hoon  ;  Lu, Shun  ;  Hayashi, Hidetoshi  ;  Felip, Enriqueta  ;  Spira, Alexander I.  ;  Girard, Nicolas  ;  Kim, Yu Jung  ;  Ostapenko, Yurii  ;  Danchaivijitr, Pongwut  ;  Liu, Baogang  ;  Alip, Adlinda  ;  Korbenfeld, Ernesto  ;  Dias, Josiane Mourao  ;  Lee, Ki Hyeong  ;  Xiong, Hailin  ;  How, Soon Hin  ;  Cheng, Ying  ;  Chang, Gee-Chen  ;  Yang, James Chih-Hsin  ;  Besse, Benjamin  ;  Thomas, Michael  ;  Shah, Sujay  ;  Baig, Mahadi  ;  Curtin, Joshua C.  ;  Zhang, Jiarui  ;  Xie, John  ;  Sun, Tao  ;  Sethi, Seema  ;  Wang, Miao  ;  Fennema, Elizabeth  ;  Daksh, Mahesh  ;  Ennis, Mariah  ;  Bauml, Joshua M.  ;  Cho, Byoung Chul 
Citation
 JOURNAL OF THORACIC ONCOLOGY, Vol.20(11) : 1655-1668, 2025-11 
Journal Title
JOURNAL OF THORACIC ONCOLOGY
ISSN
 1556-0864 
Issue Date
2025-11
MeSH
Acrylamides* / pharmacology ; Acrylamides* / therapeutic use ; Adult ; Aged ; Aniline Compounds* / pharmacology ; Aniline Compounds* / therapeutic use ; Carcinoma, Non-Small-Cell Lung* / drug therapy ; Carcinoma, Non-Small-Cell Lung* / genetics ; Carcinoma, Non-Small-Cell Lung* / pathology ; Double-Blind Method ; ErbB Receptors / genetics ; Female ; Humans ; Indoles ; Lung Neoplasms* / drug therapy ; Lung Neoplasms* / genetics ; Lung Neoplasms* / pathology ; Male ; Middle Aged ; Mutation ; Protein Kinase Inhibitors* / therapeutic use ; Pyrimidines ; Survival Rate
Keywords
EGFR-mutant NSCLC ; First-line treatment ; Laz-ertinib ; Osimertinib ; Tyrosine kinase inhibitor
Abstract
Introduction: Lazertinib is a central nervous system-penetrant, third-generation EGFR tyrosine kinase inhibitor (TKI) that was selected for combination with amivantamab due to its relatively low rates of wild-type EGFR toxicities. In the phase 3 MARIPOSA study, amivantamab plus lazertinib (amivantamab-lazertinib) significantly improved progression-free survival (PFS; p < 0.001) versus osimertinib in participants with treatment-naive EGFR-mutant advanced NSCLC. A lazertinib monotherapy arm was included to assess the contribution of components in the combination. This is the first randomized, double-blind comparison of two third-generation EGFR TKIs, lazertinib and osimertinib. Methods: In MARIPOSA, 1074 participants were randomized 2:2:1 to receive amivantamab-lazertinib (n = 429), osimertinib monotherapy (n = 429), or lazertinib mono-therapy (n = 216). This exploratory analysis compared the efficacy and safety of lazertinib and osimertinib Results: At a median follow-up of 22.0 months, median PFS was 18.5 months for lazertinib versus 16.6 months for osimertinib (hazard ratio = 0.98, 95% confidence interval: 0.79-1.22; p = 0.86). PFS results were comparable between arms among predefined subgroups. Among participants with measurable disease at baseline, objective response rate was 83% for lazertinib versus 85% for osimertinib, with a median duration of response among confirmed responders of 16.6 months versus 16.8 months, respectively. Median overall survival was not reached for both arms (hazard ratio = 1.00, 95% confidence interval: 0.73-1.38) at the interim analysis. Adverse events for both arms were mostly grades 1 to 2 and frequently related to EGFR inhibition. Lazertinib was associated with lower rates of QT interval prolongation versus osimertinib. Conclusions: Lazertinib demonstrated comparable efficacy and safety to osimertinib, including in predefined subgroups.
Files in This Item:
90341.pdf Download
DOI
10.1016/j.jtho.2025.06.030
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/209506
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links