PD-L1 as a Biomarker for the Efficacy of Durvalumab in Stage III EGFR Mutant NSCLC
- Authors
- Kim, Insu; Choi, Sun Ha; Lee, Shin Yup; Yoo, Seung Soo; Park, Ji Eun; Shin, Kyeong-Cheol; Jang, Jong Geol; Hong, Kyung Soo; Kwon, Yong Shik; Park, Sun Hyo; Choi, Keum-Ju; Jung, Chi Young; Kim, Mi-Hyun; Kim, Soo Han; Seol, Hee Yun; Kim, Jehun; Park, Jin-Han; Kim, Tae Hoon; Eom, Jung Seop; Ahn, June Hong
- Issue Date
- Oct-2024
- Publisher
- International Institute of Anticancer Research
- Keywords
- durvalumab; EGFR; NSCLC; PD-L1
- Citation
- Anticancer research, v.44, no.10, pp 4505 - 4516
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Anticancer research
- Volume
- 44
- Number
- 10
- Start Page
- 4505
- End Page
- 4516
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74828
- DOI
- 10.21873/anticanres.17279
- ISSN
- 0250-7005
1791-7530
- 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.
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