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Durvalumab, Tremelimumab, and Platinum Chemotherapy in EGFR Mutation–Positive NSCLC: An Open-Label Phase 2 Trial (ILLUMINATE)

  • Chee Khoon Lee
  • , Bin Chi Liao
  • , Shalini Subramaniam
  • , Chao Hua Chiu
  • , Antony J. Mersiades
  • , Chao Chi Ho
  • , Chris Brown
  • , Chun Liang Lai
  • , Brett G.M. Hughes
  • , Tsung Ying Yang
  • , Ken O'Byrne
  • , Yung Hung Luo
  • , Sonia Yip
  • , Ching Liang Ho
  • , Victoria Bray
  • , Wu Chou Su
  • , Melissa Moore
  • , Wei Lien Feng
  • , Ya Ying Bai
  • , Kate Ford
  • Michelle M. Cummins, Martin R. Stockler, Benjamin J. Solomon, Thomas John, James Chih-Hsin Yang

研究成果: Article › 同行評審

3   連結會在新分頁中打開 引文 斯高帕斯(Scopus)

摘要

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.

原文English
文章編號100771
期刊JTO Clinical and Research Reports
卷6
發行號2
DOIs
出版狀態Published - 2025 2月

UN SDG

此研究成果有助於以下永續發展目標

  1. SDG 3 - 良好的健康和福祉
    SDG 3 良好的健康和福祉

All Science Journal Classification (ASJC) codes

  • 腫瘤科
  • 肺和呼吸系統醫學

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