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

IF 3.5 Q2 ONCOLOGY JTO Clinical and Research Reports Pub Date : 2025-02-01 Epub Date: 2024-11-22 DOI:10.1016/j.jtocrr.2024.100771
Chee Khoon Lee PhD , Bin-Chi Liao MD , Shalini Subramaniam MMed (Clin Epi) , Chao-Hua Chiu MD , Antony J. Mersiades MMed (Clin Epi) , Chao-Chi Ho MD, PhD , Chris Brown MBiostats , Chun-Liang Lai MD, PhD , Brett G.M. Hughes M.B.B.S. (Hons) , Tsung-Ying Yang MD, PhD , Ken O’Byrne MD , Yung-Hung Luo MD, PhD , Sonia Yip PhD , Ching-Liang Ho MD , Victoria Bray PhD , Wu-Chou Su MD, PhD , Melissa Moore PhD , Wei-Lien Feng MS , Ya-Ying Bai MS , Kate Ford MHSc , James Chih-Hsin Yang MD, PhD
{"title":"Durvalumab, Tremelimumab, and Platinum Chemotherapy in EGFR Mutation–Positive NSCLC: An Open-Label Phase 2 Trial (ILLUMINATE)","authors":"Chee Khoon Lee PhD ,&nbsp;Bin-Chi Liao MD ,&nbsp;Shalini Subramaniam MMed (Clin Epi) ,&nbsp;Chao-Hua Chiu MD ,&nbsp;Antony J. Mersiades MMed (Clin Epi) ,&nbsp;Chao-Chi Ho MD, PhD ,&nbsp;Chris Brown MBiostats ,&nbsp;Chun-Liang Lai MD, PhD ,&nbsp;Brett G.M. Hughes M.B.B.S. (Hons) ,&nbsp;Tsung-Ying Yang MD, PhD ,&nbsp;Ken O’Byrne MD ,&nbsp;Yung-Hung Luo MD, PhD ,&nbsp;Sonia Yip PhD ,&nbsp;Ching-Liang Ho MD ,&nbsp;Victoria Bray PhD ,&nbsp;Wu-Chou Su MD, PhD ,&nbsp;Melissa Moore PhD ,&nbsp;Wei-Lien Feng MS ,&nbsp;Ya-Ying Bai MS ,&nbsp;Kate Ford MHSc ,&nbsp;James Chih-Hsin Yang MD, PhD","doi":"10.1016/j.jtocrr.2024.100771","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div><em>EGFR</em>-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 <em>EGFR-</em>mutant NSCLC after progression with EGFR tyrosine kinase inhibitors (TKIs).</div></div><div><h3>Methods</h3><div>Participants were treated with induction durvalumab, tremelimumab, and platinum-pemetrexed, followed by durvalumab-pemetrexed maintenance. Participants were divided into two cohorts: (1) <em>EGFR</em> 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.</div></div><div><h3>Results</h3><div>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.</div></div><div><h3>Conclusions</h3><div>Durvalumab, tremelimumab, and platinum-pemetrexed had modest anti-tumor activity in <em>EGFR-</em>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.</div></div>","PeriodicalId":17675,"journal":{"name":"JTO Clinical and Research Reports","volume":"6 2","pages":"Article 100771"},"PeriodicalIF":3.5000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11773228/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JTO Clinical and Research Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666364324001413","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Durvalumab, Tremelimumab和铂化疗治疗EGFR突变阳性NSCLC:一项开放标签2期试验(ILLUMINATE)。
egfr突变型NSCLC与低突变负荷和低水平PD-L1表达相关。我们进行了一项2期试验,以确定durvalumab、tremelimumab和铂-培美曲塞在EGFR酪氨酸激酶抑制剂(TKIs)进展后的EGFR突变型NSCLC中的疗效。方法:参与者接受诱导杜伐单抗、tremelimumab和铂-培美曲塞治疗,随后进行杜伐单抗-培美曲塞维持治疗。参与者被分为两组:(1)EGFR外显子20 T790M阴性(T790M-,一线奥西替尼治疗进展,或一线/二代TKI单线治疗进展);(2)T790M阳性(T790M+,包括奥西替尼在内的1线以上TKI治疗进展)。主要终点是研究人员评估的确定的客观缓解率(ORR)。无进展生存期和安全性是次要结局。结果:来自澳大利亚和台湾的100名参与者入组。中位随访时间为26个月,T790M-组和T790M+组分别有88%和96%出现进展事件。T790M-的ORR为31%(95%可信区间:20-45),包括两个完全应答。T790M+的ORR为21%(95%可信区间:12-34)。T790M-组和T790M+组的中位缓解持续时间分别为9.5个月和6.3个月;中位无进展生存期分别为6.5个月和4.9个月。对于T790M-, 50%及以上PD-L1的ORR为27% (n = 22), 50%及以下PD-L1的ORR为0% (n = 10)。对于T790M+, PD-L1≥50%的患者,ORR为17% (n = 24)。安全概况与以前的报告一致。结论:Durvalumab, tremelimumab和铂-培美曲塞在TKI进展后的egfr突变型NSCLC中具有适度的抗肿瘤活性。T790M组有更高的ORR和更长的反应持续时间。免疫不良事件使用tremelimumab未增加。本试验临床注册号为NCT03994393。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
期刊最新文献
Atezolizumab Combined With Cisplatin Plus Vinorelbine as Adjuvant Therapy for Completely Resected NSCLC With EGFR Mutation (West Japan Oncology Group 11719L: ADJUST Study) Treatment Timeliness in Extensive-Stage SCLC and Impact on Survival: A Registry-Based Observational Study Impacts of Multidisciplinary Lung Cancer Meeting Presentation in a Clinical Quality Registry Cost-Effectiveness of Perioperative Immune Checkpoint Therapy for NSCLC in Japan, the United States, and Brazil Brief Report: Real-World Outcomes in Patients Living With Human Immunodeficiency Virus and Lung Cancer Treated With Immune Checkpoint Inhibitors
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1