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PD-L1 as a Biomarker for the Efficacy of Durvalumab in Stage III EGFR Mutant NSCLC
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Insu | - |
| dc.contributor.author | Choi, Sun Ha | - |
| dc.contributor.author | Lee, Shin Yup | - |
| dc.contributor.author | Yoo, Seung Soo | - |
| dc.contributor.author | Park, Ji Eun | - |
| dc.contributor.author | Shin, Kyeong-Cheol | - |
| dc.contributor.author | Jang, Jong Geol | - |
| dc.contributor.author | Hong, Kyung Soo | - |
| dc.contributor.author | Kwon, Yong Shik | - |
| dc.contributor.author | Park, Sun Hyo | - |
| dc.contributor.author | Choi, Keum-Ju | - |
| dc.contributor.author | Jung, Chi Young | - |
| dc.contributor.author | Kim, Mi-Hyun | - |
| dc.contributor.author | Kim, Soo Han | - |
| dc.contributor.author | Seol, Hee Yun | - |
| dc.contributor.author | Kim, Jehun | - |
| dc.contributor.author | Park, Jin-Han | - |
| dc.contributor.author | Kim, Tae Hoon | - |
| dc.contributor.author | Eom, Jung Seop | - |
| dc.contributor.author | Ahn, June Hong | - |
| dc.date.accessioned | 2024-12-03T08:30:54Z | - |
| dc.date.available | 2024-12-03T08:30:54Z | - |
| dc.date.issued | 2024-10 | - |
| dc.identifier.issn | 0250-7005 | - |
| dc.identifier.issn | 1791-7530 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/74828 | - |
| dc.description.abstract | BACKGROUND/AIM: Durvalumab consolidation is less effective in patients with epidermal growth factor receptor mutant (EGFR M+) NSCLC. Studies of durvalumab on EGFR M+ NSCLC as an expression of programmed death-ligand 1 (PD-L1) expression are limited. The purpose of this study was to determine the effect of durvalumab on PD-L1 expression in EGFR M+ patients. PATIENTS AND METHODS: This study included 249 unresectable stage III NSCLC patients treated with durvalumab. The primary outcome was progression-free survival (PFS). Cox multivariate analysis was performed based on EGFR and PD-L1 statuses: EGFR M-, PD-L1 ≥50% (cohort A); EGFR M-, PD-L1 <50% (cohort B); EGFR M+, PD-L1 ≥50% (cohort C); and EGFR M+, PD-L1 <50% (cohort D). RESULTS: Overall, 31 of 249 (12.4%) and 218 of the 249 (87.6%) patients had EGFR M+ and EGFR M- NSCLC, respectively. Median PFSs and OSs did not differ (PFS: 16.6 vs. 18.7 months, p=0.591; OS: 37.4 vs. 35.7 months, p=0.271). Median PFS of cohort A did not significantly differ from the median PFSs of cohorts B and C, but it was significantly longer than the median PFS of cohort D (23.7 vs. 15.2 months, p=0.045). Cox multivariate analysis revealed that cohort D exhibited a worse PFS (adjusted hazard ratio=2.27, 95% confidence interval=1.11-4.66, p=0.025) compared with cohort A. Median OSs were not different between the four cohorts. CONCLUSION: Durvalumab consolidation provided similar benefit in EGFR M+ patients with PD-L1 ≥50% compared with EGFR M- patients. A therapeutic role of durvalumab in patients with EGFR M+, high PD-L1 unresectable stage III NSCLC should be considered. Copyright © 2024 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. | - |
| dc.format.extent | 12 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | International Institute of Anticancer Research | - |
| dc.title | PD-L1 as a Biomarker for the Efficacy of Durvalumab in Stage III EGFR Mutant NSCLC | - |
| dc.type | Article | - |
| dc.publisher.location | 그리이스 | - |
| dc.identifier.doi | 10.21873/anticanres.17279 | - |
| dc.identifier.scopusid | 2-s2.0-85205447127 | - |
| dc.identifier.wosid | 001341472700006 | - |
| dc.identifier.bibliographicCitation | Anticancer research, v.44, no.10, pp 4505 - 4516 | - |
| dc.citation.title | Anticancer research | - |
| dc.citation.volume | 44 | - |
| dc.citation.number | 10 | - |
| dc.citation.startPage | 4505 | - |
| dc.citation.endPage | 4516 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Oncology | - |
| dc.relation.journalWebOfScienceCategory | Oncology | - |
| dc.subject.keywordPlus | CELL LUNG-CANCER | - |
| dc.subject.keywordPlus | CHEMORADIOTHERAPY | - |
| dc.subject.keywordPlus | MUTATIONS | - |
| dc.subject.keywordAuthor | durvalumab | - |
| dc.subject.keywordAuthor | EGFR | - |
| dc.subject.keywordAuthor | NSCLC | - |
| dc.subject.keywordAuthor | PD-L1 | - |
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