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Title: | Durvalumab, Tremelimumab, and Platinum Chemotherapy in EGFR Mutation?Positive NSCLC: An Open-Label Phase 2 Trial (ILLUMINATE) |
Author: | Lee, C. K. Liao, B. C. Subramaniam, S. Chiu, C. H. Mersiades, A. J. Ho, C. C. Brown, C. Lai, C. L. Hughes, B. G. M. Yang, T. Y. O'Byrne, K. Luo, Y. H. Yip, S. Ho, C. L. Bray, V. Su, W. C. Moore, M. Feng, W. L. Bai, Y. Y. Ford, K. Cummins, M. M. Stockler, M. R. Solomon, B. J. John, T. Chih-Hsin Yang, J. |
Issue Date: | 2025 |
Journal: | JTO Clinical and Research Reports |
Abstract: | Introduction: EGFR-mutant NSCLC is associated with low mutation burden and low levels of PD-L1 expression. We conducted a phase 2 trial to determine the efficacy of durvalumab, tremelimumab, and platinum-pemetrexed in EGFR-mutant NSCLC after progression with EGFR tyrosine kinase inhibitors (TKIs). Methods: Participants were treated with induction durvalumab, tremelimumab, and platinum-pemetrexed, followed by durvalumab-pemetrexed maintenance. Participants were divided into two cohorts: (1) EGFR exon 20 T790M negative (T790M?, progressing on either first-line osimertinib, or on a single line of first/second generation TKI), and (2) T790M positive (T790M+, progressing on greater than or equal to 1 lines of TKI, including osimertinib). The primary endpoint was the confirmed objective response rate (ORR) assessed by the investigators. Progression-free survival and safety were secondary outcomes. Results: One hundred participants from Australia and Taiwan were enrolled. Median follow-up was 26 months with 88% and 96% experiencing progression events for T790M? and T790M+, respectively. The ORR for T790M? was 31% (95% confidence interval: 20?45), including two complete responses. The ORR for T790M+ was 21% (95% confidence interval: 12?34). Median durations of response were 9.5 months and 6.3 months for T790M? and T790M+, respectively; median progression-free survival rates were 6.5 months and 4.9 months, respectively. For T790M?, ORR was 27% for 50% or higher PD-L1 (n = 22) and 0% for less than 50% PD-L1 (n = 10), respectively. For T790M+, ORR was 17% for 50% or higher PD-L1 (n = 24). The safety profile was consistent with previous reports. Conclusions: Durvalumab, tremelimumab, and platinum-pemetrexed had modest anti-tumor activity in EGFR-mutant NSCLC after progression on TKI. The T790M? cohort had higher ORR and a longer duration of response. Immune adverse events were not increased with tremelimumab. The clinical registration number of this trial is NCT03994393. � 2024 The Authors |
ISSN: | 26663643 (ISSN) |
Digital object identifier: | 10.1016/j.jtocrr.2024.100771 |
URI: | https://swslhd.intersearch.com.au/swslhdjspui/handle/1/13319 |
Appears in Collections: | Liverpool Hospital |
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