Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/13319
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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