Cited 0 times in 
Cited 0 times in 
Overall survival for amivantamab plus lazertinib versus osimertinib as first-line treatment in Asian participants with EGFR-mutant advanced NSCLC: A MARIPOSA subset analysis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hayashi, Hidetoshi | - |
| dc.contributor.author | Cho, Byoung Chul | - |
| dc.contributor.author | Kim, Yu Jung | - |
| dc.contributor.author | Lee, Se-Hoon | - |
| dc.contributor.author | Danchaivijitr, Pongwut | - |
| dc.contributor.author | Alip, Adlinda | - |
| dc.contributor.author | Xiong, Hailin | - |
| dc.contributor.author | How, Soon-Hin | - |
| dc.contributor.author | Chang, Gee-Chen | - |
| dc.contributor.author | Yang, James Chih-Hsin | - |
| dc.contributor.author | Yamanaka, Yuta | - |
| dc.contributor.author | Sendur, Mehmet Ali Nahit | - |
| dc.contributor.author | Prabhash, Kumar | - |
| dc.contributor.author | Azuma, Koichi | - |
| dc.contributor.author | Akawung, Alianu | - |
| dc.contributor.author | Fennema, Elizabeth | - |
| dc.contributor.author | Tang, Xiaodan | - |
| dc.contributor.author | Shah, Sujay | - |
| dc.contributor.author | Sethi, Seema | - |
| dc.contributor.author | Lu, Shun | - |
| dc.date.accessioned | 2026-03-27T02:13:13Z | - |
| dc.date.available | 2026-03-27T02:13:13Z | - |
| dc.date.created | 2026-03-20 | - |
| dc.date.issued | 2026-04 | - |
| dc.identifier.issn | 0169-5002 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/211536 | - |
| dc.description.abstract | Background: Approximately 60 % of lung cancer cases occur in Asia, indicating an epidemiological disparity and need for effective therapies. Amivantamab-lazertinib is approved for first-line EGFR-mutated advanced non-small cell lung cancer (NSCLC) in many countries. In the protocol-specified final overall survival (OS) analysis of MARIPOSA (NCT04487080), amivantamab-lazertinib showed a statistically significant and clinically meaningful improvement in OS versus osimertinib (HR, 0.75; P = 0.005) among all participants. We evaluated OS for amivantamab-lazertinib versus osimertinib in Asian participants. Patients and methods: Participants with previously untreated EGFR-mutated, locally advanced/metastatic NSCLC were randomized 2:2:1 to receive amivantamab-lazertinib, osimertinib, or lazertinib (for evaluating contribution of components). Self-identified Asian race was a stratification factor. OS was a key secondary endpoint. Results: Of 1074 randomized participants, 629 self-identified as Asian (amivantamab-lazertinib:250; osimertinib:251; lazertinib:128). At a median follow-up of 38.7 months, amivantamab-lazertinib significantly prolonged OS versus osimertinib among Asian participants. Median OS was not reached (NR; 95 % CI, NR-NR) for amivantamab-lazertinib versus 38.4 months (95 % CI, 35.1-NR) for osimertinib (HR, 0.74; 95 % CI, 0.56-0.97; nominal P = 0.026). Assuming exponential distribution of OS in both arms, amivantamab-lazertinib is projected to prolong median OS among Asian participants by > 12 months versus osimertinib. At 36 months, 61 % and 53 % were alive in the amivantamab-lazertinib and osimertinib arms. Safety profile was consistent with the overall population. Conclusions: Consistent with the overall population, amivantamab-lazertinib significantly improved OS versus osimertinib among Asian participants with previously untreated EGFR-mutated advanced NSCLC, making it the first regimen to improve survival among Asian patients. | - |
| dc.language | English | - |
| dc.publisher | Elsevier Scientific Publishers | - |
| dc.relation.isPartOf | LUNG CANCER | - |
| dc.relation.isPartOf | LUNG CANCER | - |
| dc.subject.MESH | Acrylamides* / administration & dosage | - |
| dc.subject.MESH | Acrylamides* / therapeutic use | - |
| dc.subject.MESH | Adult | - |
| dc.subject.MESH | Aged | - |
| dc.subject.MESH | Aged, 80 and over | - |
| dc.subject.MESH | Aniline Compounds* / administration & dosage | - |
| dc.subject.MESH | Aniline Compounds* / therapeutic use | - |
| dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols* / therapeutic use | - |
| dc.subject.MESH | Asian People / genetics | - |
| dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / drug therapy | - |
| dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / genetics | - |
| dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / mortality | - |
| dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / pathology | - |
| dc.subject.MESH | ErbB Receptors / genetics | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Indoles | - |
| dc.subject.MESH | Lung Neoplasms* / drug therapy | - |
| dc.subject.MESH | Lung Neoplasms* / genetics | - |
| dc.subject.MESH | Lung Neoplasms* / mortality | - |
| dc.subject.MESH | Lung Neoplasms* / pathology | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Mutation* | - |
| dc.subject.MESH | Pyrimidines | - |
| dc.subject.MESH | Treatment Outcome | - |
| dc.title | Overall survival for amivantamab plus lazertinib versus osimertinib as first-line treatment in Asian participants with EGFR-mutant advanced NSCLC: A MARIPOSA subset analysis | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Hayashi, Hidetoshi | - |
| dc.contributor.googleauthor | Cho, Byoung Chul | - |
| dc.contributor.googleauthor | Kim, Yu Jung | - |
| dc.contributor.googleauthor | Lee, Se-Hoon | - |
| dc.contributor.googleauthor | Danchaivijitr, Pongwut | - |
| dc.contributor.googleauthor | Alip, Adlinda | - |
| dc.contributor.googleauthor | Xiong, Hailin | - |
| dc.contributor.googleauthor | How, Soon-Hin | - |
| dc.contributor.googleauthor | Chang, Gee-Chen | - |
| dc.contributor.googleauthor | Yang, James Chih-Hsin | - |
| dc.contributor.googleauthor | Yamanaka, Yuta | - |
| dc.contributor.googleauthor | Sendur, Mehmet Ali Nahit | - |
| dc.contributor.googleauthor | Prabhash, Kumar | - |
| dc.contributor.googleauthor | Azuma, Koichi | - |
| dc.contributor.googleauthor | Akawung, Alianu | - |
| dc.contributor.googleauthor | Fennema, Elizabeth | - |
| dc.contributor.googleauthor | Tang, Xiaodan | - |
| dc.contributor.googleauthor | Shah, Sujay | - |
| dc.contributor.googleauthor | Sethi, Seema | - |
| dc.contributor.googleauthor | Lu, Shun | - |
| dc.identifier.doi | 10.1016/j.lungcan.2026.109305 | - |
| dc.relation.journalcode | J02174 | - |
| dc.identifier.eissn | 1872-8332 | - |
| dc.identifier.pmid | 41689889 | - |
| dc.subject.keyword | Asian | - |
| dc.subject.keyword | Amivantamab plus lazertinib | - |
| dc.subject.keyword | Overall survival | - |
| dc.subject.keyword | EGFR-mutated NSCLC | - |
| dc.subject.keyword | EGFR TKI | - |
| dc.contributor.affiliatedAuthor | Cho, Byoung Chul | - |
| dc.identifier.scopusid | 2-s2.0-105030134618 | - |
| dc.identifier.wosid | 001694682300001 | - |
| dc.citation.volume | 214 | - |
| dc.identifier.bibliographicCitation | LUNG CANCER, Vol.214, 2026-04 | - |
| dc.identifier.rimsid | 92077 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Asian | - |
| dc.subject.keywordAuthor | Amivantamab plus lazertinib | - |
| dc.subject.keywordAuthor | Overall survival | - |
| dc.subject.keywordAuthor | EGFR-mutated NSCLC | - |
| dc.subject.keywordAuthor | EGFR TKI | - |
| dc.subject.keywordPlus | CELL LUNG-CANCER | - |
| dc.subject.keywordPlus | BRAIN METASTASES | - |
| dc.subject.keywordPlus | MUTATION | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Oncology | - |
| dc.relation.journalWebOfScienceCategory | Respiratory System | - |
| dc.relation.journalResearchArea | Oncology | - |
| dc.relation.journalResearchArea | Respiratory System | - |
| dc.identifier.articleno | 109305 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.