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Amivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 조병철 | - |
| dc.date.accessioned | 2025-09-02T08:16:38Z | - |
| dc.date.available | 2025-09-02T08:16:38Z | - |
| dc.date.issued | 2025-06 | - |
| dc.identifier.issn | 0169-5002 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/207240 | - |
| dc.description.abstract | Introduction: The incidence of epidermal growth factor receptor (EGFR) mutations is higher among Asian patients with advanced non-small cell lung cancer than the general advanced non-small cell lung cancer population. We evaluated the efficacy and safety of amivantamab in combination with lazertinib versus osimertinib in Asian participants from the phase 3 MARIPOSA study who had treatment-naïve advanced non-small cell lung cancer with common EGFR mutations. Methods: Participants were randomized 2:2:1 to receive amivantamab-lazertinib, osimertinib alone, or lazertinib alone. The primary endpoint was progression-free survival based on blinded independent central review per RECIST v1.1. Secondary endpoints included overall survival, objective response rate, duration of response, and safety. Exploratory endpoints included extracranial progression-free survival and post-progression outcomes. Results: Of 1074 randomized participants, 629 were Asian, with 250 and 251 randomized to the amivantamab-lazertinib and osimertinib arms, respectively. Among Asian participants, at a median follow-up of 22.5 months, amivantamab-lazertinib showed a 35 % reduction in the risk of disease progression or death versus osimertinib (hazard ratio, 0.65; P < 0.001). Consistent with the overall population, median progression-free survival was 27.5 and 18.3 months in the amivantamab-lazertinib and osimertinib arms, respectively. The objective response rate was 88 % for amivantamab-lazertinib versus 85 % for osimertinib. The median duration of response among confirmed responders improved by 8.6 months for amivantamab-lazertinib versus osimertinib. Favorable trends were also seen for overall survival, extracranial progression-free survival, and post-progression outcomes for amivantamab-lazertinib over osimertinib. Adverse events in Asian participants were similar to those in the overall population. Conclusions: Amivantamab-lazertinib demonstrated superior progression-free survival versus osimertinib in Asian participants, with a tolerable safety profile. These results were consistent with those in the overall population. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | Elsevier Scientific Publishers | - |
| dc.relation.isPartOf | LUNG CANCER | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.subject.MESH | Acrylamides* / administration & dosage | - |
| dc.subject.MESH | Acrylamides* / therapeutic use | - |
| dc.subject.MESH | Adult | - |
| dc.subject.MESH | Aged | - |
| 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 | Amivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Byoung Chul Cho | - |
| dc.contributor.googleauthor | Hidetoshi Hayashi | - |
| dc.contributor.googleauthor | Jong-Seok Lee | - |
| dc.contributor.googleauthor | Se-Hoon Lee | - |
| dc.contributor.googleauthor | Pongwut Danchaivijitr | - |
| dc.contributor.googleauthor | Ying Cheng | - |
| dc.contributor.googleauthor | Baogang Liu | - |
| dc.contributor.googleauthor | Adlinda Alip | - |
| dc.contributor.googleauthor | Hailin Xiong | - |
| dc.contributor.googleauthor | Soon Hin How | - |
| dc.contributor.googleauthor | Gee-Chen Chang | - |
| dc.contributor.googleauthor | James Chih-Hsin Yang | - |
| dc.contributor.googleauthor | Hiroshige Yoshioka | - |
| dc.contributor.googleauthor | Mehmet Ali Nahit Şendur | - |
| dc.contributor.googleauthor | Kumar Prabhash | - |
| dc.contributor.googleauthor | Koichi Azuma | - |
| dc.contributor.googleauthor | Yun-Gyoo Lee | - |
| dc.contributor.googleauthor | Chien-Chung Lin | - |
| dc.contributor.googleauthor | Shingo Matsumoto | - |
| dc.contributor.googleauthor | Patrapim Sunpaweravong | - |
| dc.contributor.googleauthor | Yichuan Xia | - |
| dc.contributor.googleauthor | Melissa Martinez | - |
| dc.contributor.googleauthor | Joshua M Bauml | - |
| dc.contributor.googleauthor | Seema Sethi | - |
| dc.contributor.googleauthor | Shun Lu | - |
| dc.identifier.doi | 10.1016/j.lungcan.2025.108496 | - |
| dc.contributor.localId | A03822 | - |
| dc.relation.journalcode | J02174 | - |
| dc.identifier.eissn | 1872-8332 | - |
| dc.identifier.pmid | 40300278 | - |
| dc.subject.keyword | Amivantamab | - |
| dc.subject.keyword | Asian patient | - |
| dc.subject.keyword | EGFR TKI | - |
| dc.subject.keyword | EGFR-mutated NSCLC | - |
| dc.contributor.alternativeName | Cho, Byoung Chul | - |
| dc.contributor.affiliatedAuthor | 조병철 | - |
| dc.citation.volume | 204 | - |
| dc.citation.startPage | 108496 | - |
| dc.identifier.bibliographicCitation | LUNG CANCER, Vol.204 : 108496, 2025-06 | - |
| dc.identifier.rimsid | 88874 | - |
| dc.type.rims | ART | - |
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