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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
  • The University of Sydney
  • National Taiwan University
  • Taipei Medical University
  • Buddhist Tzu Chi Medical Foundation
  • University of Queensland
  • Prince Charles Hospital
  • Veterans General Hospital-Taichung Taiwan
  • Queensland University of Technology
  • Veterans General Hospital-Taipei
  • Triservice General Hospital Taiwan
  • Liverpool Hospital
  • National Cheng Kung University
  • St. Vincent's Hospital Melbourne
  • National Health Research Institutes Taiwan
  • Peter Maccallum Cancer Centre

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

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.
Original languageEnglish
Article number100771
Number of pages11
JournalJTO Clinical and Research Reports
Volume6
Issue number2
DOIs
Publication statusPublished - Feb 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Checkpoint inhibitors
  • Chemotherapy
  • EGFR mutation
  • Non-small cell lung cancer

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