一项开放标签,随机III期研究,在标准一线铂基化疗后,晚期鳞状非小细胞肺癌(NSCLC)患者早期切换维持与延迟二线纳沃单抗- eden试验。

IF 4.5 2区 医学 Q1 ONCOLOGY Lung Cancer Pub Date : 2024-12-15 DOI:10.1016/j.lungcan.2024.108059
Francesco Gelsomino, Luca Boni, Marcello Tiseo, Serena Ricciardi, Danilo Rocco, Diego L Cortinovis, Manuela Proietto, Alessio Cogoni, Giulia Pasello, Andrea Camerini, Francesca Sperandi, Ida Colantonio, Giulio Metro, Francesca Mazzoni, Editta Baldini, Antonello Veccia, Elisa Bennicelli, Anna Cecilia Bettini, Michele Tognetto, Andrea Ardizzoni
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引用次数: 0

摘要

背景:对于鳞状(Sq)-NSCLC, Checkmate-017试验显示,在二线治疗中,尼武单抗(Nivo)比多西他赛有显著的总生存期(OS)改善。我们假设预期Nivo的使用,作为一线化疗(CHT)后的早期切换维护,与延迟的二线治疗相比,可能会提高生存率。方法:EDEN是一项开放标签,2组,III期研究,随机(1:1)III期ib /IV期sqnsclc患者在一线铂基CHT后未进展,接受早期Nivo作为切换维持(A组)或标准最佳支持治疗,然后在疾病进展时接受二线Nivo (B组)。在两个组中,Nivo以每2周240 mg的剂量静脉注射,直到疾病进展,无法忍受的毒性,或最多2年。主要终点为OS。结果:从2017年9月到2020年8月,从32个意大利中心随机抽取125例患者(62例A组vs 63例B组)。由于一线的icpi注册,在达到计划样本量(388 pts)之前,预计工作提前停止。大多数患者为男性(79.2%),目前/曾经吸烟者(93.6%),IV期(74.4%),表现状态0-1(98.4%)。A组的mOS (95% CI)为14.9(10.4-18.6)个月,B组为18.8(14.4-21.1)个月(HR 1.09, 95% CI 0.74-1.62, p = 0.659)。结论:在晚期Sq-NSCLC中,使用Nivo作为一线CHT后的切换维护,与使用Nivo作为二线相比,并没有改善OS。虽然icpi的最佳使用仍然在第一线,但其作为维护的作用必须得到更好的研究。临床试验:gov:注册号:NCT03542461。
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An open-label, randomized phase III study of early switch maintenance vs delayed second-line nivolumab in advanced stage squamous non-small cell lung cancer (NSCLC) patients after standard first-line platinum-based chemotherapy-EDEN trial GOIRC 04-2016.

Background: As for squamous (Sq)-NSCLC, Checkmate-017 trial showed a significant overall survival (OS) improvement in favor of Nivolumab (Nivo) over Docetaxel in 2nd-line. We hypothesized that anticipating Nivo use, as early switch maintenance after 1st-line chemotherapy (CHT), might have improved survival as compared to delayed 2nd-line treatment.

Methods: EDEN was an open-label, 2-arm, phase III study which randomized (1:1) stage IIIB/IV Sq-NSCLC pts non-progressive after 1st-line platinum-based CHT, to receive early Nivo as switch maintenance (Arm A) or standard best supportive care followed by 2nd-line Nivo at disease progression (Arm B). In both arms, Nivo was administered at the dose of 240 mg i.v. every 2 weeks until progressive disease, intolerable toxicity, or for a maximum of 2 years. The primary endpoint was OS.

Results: From Sep 2017 to Aug 2020 125 patients (62 Arm A vs 63 Arm B) were randomized from 32 Italian centers. Accrual was stopped early, before the planned sample size (388 pts) was reached, because of registration of ICPIs in 1st-line. Most patients were male (79.2 %), current/former smokers (93.6 %), had stage IV (74.4 %), performance status 0-1 (98.4 %). mOS (95 % CI) was 14.9 (10.4-18.6) months in arm A vs 18.8 (14.4-21.1) months in arm B (HR 1.09, 95 %CI 0.74-1.62, p = 0.659).

Conclusions: In advanced Sq-NSCLC, the use of Nivo as switch maintenance after 1st-line CHT, does not improve OS compared to its use as 2nd-line. Although the optimal use of ICPIs remains in 1st-line, its role as maintenance has to be better investigated.

Clinicaltrials: gov: registration number: NCT03542461.

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来源期刊
Lung Cancer
Lung Cancer 医学-呼吸系统
CiteScore
9.40
自引率
3.80%
发文量
407
审稿时长
25 days
期刊介绍: Lung Cancer is an international publication covering the clinical, translational and basic science of malignancies of the lung and chest region.Original research articles, early reports, review articles, editorials and correspondence covering the prevention, epidemiology and etiology, basic biology, pathology, clinical assessment, surgery, chemotherapy, radiotherapy, combined treatment modalities, other treatment modalities and outcomes of lung cancer are welcome.
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