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PD-L1 as a Biomarker for the Efficacy of Durvalumab in Stage III EGFR Mutant NSCLC

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dc.contributor.authorKim, Insu-
dc.contributor.authorChoi, Sun Ha-
dc.contributor.authorLee, Shin Yup-
dc.contributor.authorYoo, Seung Soo-
dc.contributor.authorPark, Ji Eun-
dc.contributor.authorShin, Kyeong-Cheol-
dc.contributor.authorJang, Jong Geol-
dc.contributor.authorHong, Kyung Soo-
dc.contributor.authorKwon, Yong Shik-
dc.contributor.authorPark, Sun Hyo-
dc.contributor.authorChoi, Keum-Ju-
dc.contributor.authorJung, Chi Young-
dc.contributor.authorKim, Mi-Hyun-
dc.contributor.authorKim, Soo Han-
dc.contributor.authorSeol, Hee Yun-
dc.contributor.authorKim, Jehun-
dc.contributor.authorPark, Jin-Han-
dc.contributor.authorKim, Tae Hoon-
dc.contributor.authorEom, Jung Seop-
dc.contributor.authorAhn, June Hong-
dc.date.accessioned2024-12-03T08:30:54Z-
dc.date.available2024-12-03T08:30:54Z-
dc.date.issued2024-10-
dc.identifier.issn0250-7005-
dc.identifier.issn1791-7530-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/74828-
dc.description.abstractBACKGROUND/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.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherInternational Institute of Anticancer Research-
dc.titlePD-L1 as a Biomarker for the Efficacy of Durvalumab in Stage III EGFR Mutant NSCLC-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.doi10.21873/anticanres.17279-
dc.identifier.scopusid2-s2.0-85205447127-
dc.identifier.wosid001341472700006-
dc.identifier.bibliographicCitationAnticancer research, v.44, no.10, pp 4505 - 4516-
dc.citation.titleAnticancer research-
dc.citation.volume44-
dc.citation.number10-
dc.citation.startPage4505-
dc.citation.endPage4516-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusCHEMORADIOTHERAPY-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordAuthordurvalumab-
dc.subject.keywordAuthorEGFR-
dc.subject.keywordAuthorNSCLC-
dc.subject.keywordAuthorPD-L1-
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