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在局部晚期非小细胞肺癌患者中同步放化疗中添加二甲双胍:NRG-LU001 期 2 随机临床试验。

Addition of Metformin to Concurrent Chemoradiation in Patients With Locally Advanced Non-Small Cell Lung Cancer: The NRG-LU001 Phase 2 Randomized Clinical Trial.

机构信息

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.

NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania.

出版信息

JAMA Oncol. 2021 Sep 1;7(9):1324-1332. doi: 10.1001/jamaoncol.2021.2318.

Abstract

IMPORTANCE

Non-small cell lung cancer (NSCLC) has relatively poor outcomes. Metformin has significant data supporting its use as an antineoplastic agent.

OBJECTIVE

To compare chemoradiation alone vs chemoradiation and metformin in stage III NSCLC.

DESIGN, SETTING, AND PARTICIPANTS: The NRG-LU001 randomized clinical trial was an open-label, phase 2 study conducted from August 24, 2014, to December 15, 2016. Patients without diabetes who were diagnosed with unresectable stage III NSCLC were stratified by performance status, histology, and stage. The setting was international and multi-institutional. This study examined prespecified endpoints, and data were analyzed on an intent-to-treat basis. Data were analyzed from February 25, 2019, to March 6, 2020.

INTERVENTIONS

Chemoradiation and consolidation chemotherapy with or without metformin.

MAIN OUTCOMES AND MEASURES

The primary outcome was 1-year progression-free survival (PFS), designed to detect 15% improvement in 1-year PFS from 50% to 65% (hazard ratio [HR], 0.622). Secondary end points included overall survival, time to local-regional recurrence, time to distant metastasis, and toxicity per Common Terminology Criteria for Adverse Events, version 4.03.

RESULTS

A total of 170 patients were enrolled, with 167 eligible patients analyzed after exclusions (median age, 64 years [interquartile range, 58-72 years]; 97 men [58.1%]; 137 White patients [82.0%]), with 81 in the control group and 86 in the metformin group. Median follow-up was 27.7 months (range, 0.03-47.21 months) among living patients. One-year PFS rates were 60.4% (95% CI, 48.5%-70.4%) in the control group and 51.3% (95% CI, 39.8%-61.7%) in the metformin group (HR, 1.15; 95% CI, 0.77-1.73; P = .24). Clinical stage was the only factor significantly associated with PFS on multivariable analysis (HR, 1.79; 95% CI, 1.19-2.69; P = .005). One-year overall survival was 80.2% (95% CI, 69.3%-87.6%) in the control group and 80.8% (95% CI, 70.2%-87.9%) in the metformin group. There were no significant differences in local-regional recurrence or distant metastasis at 1 or 2 years. No significant difference in adverse events was observed between treatment groups.

CONCLUSIONS AND RELEVANCE

In this randomized clinical trial, the addition of metformin to concurrent chemoradiation was well tolerated but did not improve survival among patients with unresectable stage III NSCLC.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT02186847.

摘要

重要性

非小细胞肺癌(NSCLC)的预后相对较差。二甲双胍在作为抗肿瘤药物方面有大量数据支持。

目的

比较单纯放化疗与放化疗联合二甲双胍治疗 III 期非小细胞肺癌。

设计、地点和参与者:NRG-LU001 是一项开放标签、2 期临床试验,于 2014 年 8 月 24 日至 2016 年 12 月 15 日进行。未被诊断为不可切除的 III 期非小细胞肺癌的患者,按体力状态、组织学和分期进行分层。该研究是国际性的和多机构的。本研究检查了预设终点,并基于意向治疗进行了数据分析。数据分析于 2019 年 2 月 25 日至 2020 年 3 月 6 日进行。

干预措施

放化疗和巩固化疗联合或不联合二甲双胍。

主要观察结果和措施

主要终点是 1 年无进展生存率(PFS),旨在检测 1 年 PFS 从 50%提高到 65%(风险比[HR],0.622)。次要终点包括总生存、局部区域复发时间、远处转移时间和按照通用不良事件术语标准 4.03 版的毒性。

结果

共纳入 170 例患者,排除后 167 例符合条件的患者进行了分析(中位年龄 64 岁[四分位距 58-72 岁];男性 97 例[58.1%];白人 137 例[82.0%]),对照组 81 例,二甲双胍组 86 例。生存患者的中位随访时间为 27.7 个月(范围 0.03-47.21 个月)。对照组的 1 年 PFS 率为 60.4%(95%CI,48.5%-70.4%),二甲双胍组为 51.3%(95%CI,39.8%-61.7%)(HR,1.15;95%CI,0.77-1.73;P=0.24)。多变量分析显示,临床分期是唯一与 PFS 显著相关的因素(HR,1.79;95%CI,1.19-2.69;P=0.005)。对照组的 1 年总生存率为 80.2%(95%CI,69.3%-87.6%),二甲双胍组为 80.8%(95%CI,70.2%-87.9%)。1 年和 2 年时,局部区域复发或远处转移无显著差异。治疗组之间未观察到不良反应的显著差异。

结论和相关性

在这项随机临床试验中,在同步放化疗中加入二甲双胍可耐受,但不能提高不可切除的 III 期非小细胞肺癌患者的生存率。

试验注册

ClinicalTrials.gov 标识符:NCT02186847。

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