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二甲双胍联合放化疗治疗局部晚期非小细胞肺癌:OCOG-ALMERA 随机临床试验。

Metformin in Combination With Chemoradiotherapy in Locally Advanced Non-Small Cell Lung Cancer: The OCOG-ALMERA Randomized Clinical Trial.

机构信息

Juravinski Cancer Center, Hamilton Health Science, Hamilton, Ontario, Canada.

Department of Oncology, McMaster University, Hamilton, Ontario, Canada.

出版信息

JAMA Oncol. 2021 Sep 1;7(9):1333-1341. doi: 10.1001/jamaoncol.2021.2328.

DOI:10.1001/jamaoncol.2021.2328
PMID:34323924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8323053/
Abstract

IMPORTANCE

Unresected locally advanced non-small cell lung cancer (LA-NSCLC) shows poor survival outcomes even after aggressive concurrent chemoradiotherapy. Whether metformin, a diabetes agent that inhibits the mitochondria oxidative phosphorylation chain, could improve radiotherapy and chemotherapy response in LA-NSCLC remains to be studied.

OBJECTIVE

To examine whether metformin, given concurrently with chemoradiotherapy and as consolidation treatment, could improve outcomes in patients with LA-NSCLC.

DESIGN, SETTING, AND PARTICIPANTS: The Ontario Clinical Oncology Group Advanced Lung Cancer Treatment With Metformin and Chemoradiotherapy (OCOG-ALMERA) study was a multicenter phase 2 randomized clinical trial. Patients were stratified for stage IIIA vs IIIB LA-NSCLC and use of consolidation chemotherapy. The trial was designed to enroll 96 patients with unresected LA-NSCLC who did not have diabetes. The trial was conducted from September 24, 2014, to March 8, 2019.

INTERVENTIONS

Patients were randomized to platinum-based chemotherapy, concurrent with chest radiotherapy (60-63 Gy), with or without consolidation chemotherapy or the same treatment plus metformin, 2000 mg/d, during chemoradiotherapy and afterward for up to 12 months.

MAIN OUTCOMES AND MEASURES

The primary outcome was the proportion of patients who experienced a failure event (ie, locoregional disease progression, distant metastases, death, and discontinuation of trial treatment or planned evaluations for any reason within 12 months). Proportions were compared using a 2-sided Fisher exact test. Conventional progression-free and overall survival were estimated using the Kaplan-Meier method. Adverse events were graded with Common Terminology Criteria for Adverse Events, version 4.03. All randomized patients were included in an intention-to-treat analysis.

RESULTS

The trial was stopped early due to slow accrual. Between 2014 and 2019, 54 patients were randomized (26 in experimental arm and 28 in control arm). Participants included 30 women (55.6%); mean (SD) age was 65.6 (7.6) years. Treatment failure was detected in 18 patients (69.2%) receiving metformin within 1 year vs 12 (42.9%) control patients (P = .05). The 1-year progression-free survival rate was 34.8% (95% CI, 16.6%-53.7%) in the metformin arm and 63.0% (95% CI, 42.1%-78.1%) in the control arm (hazard ratio, 2.42; 95% CI, 1.14-5.10) The overall survival rates were 47.4% (95% CI, 26.3%-65.9%) in the metformin arm and 85.2% (95% CI, 65.2%-94.2%) in the control arm (hazard ratio, 3.80; 95% CI, 1.49-9.73). More patients in the experimental arm vs control arm (53.8% vs 25.0%) reported at least 1 grade 3 or higher adverse event.

CONCLUSIONS AND RELEVANCE

In this randomized clinical trial, the addition of metformin to chemoradiotherapy was associated with worse treatment efficacy and increased toxic effects compared with combined modality therapy alone. Metformin is not recommended in patients with LA-NSCLC who are candidates for chemoradiotherapy.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT02115464.

摘要

重要性

未经切除的局部晚期非小细胞肺癌(LA-NSCLC)即使接受积极的同步放化疗,生存结局也较差。二甲双胍是一种抑制线粒体氧化磷酸化链的糖尿病药物,它是否能改善 LA-NSCLC 的放疗和化疗反应仍有待研究。

目的

研究二甲双胍在与放化疗同时使用并作为巩固治疗时,是否能改善 LA-NSCLC 患者的结局。

设计、地点和参与者:安大略临床肿瘤组高级肺癌治疗联合二甲双胍和放化疗(OCOG-ALMERA)研究是一项多中心的 2 期随机临床试验。患者按 IIIA 期与 IIIB 期 LA-NSCLC 和巩固化疗的使用进行分层。该试验设计招募 96 名未经手术的 LA-NSCLC 患者,这些患者没有糖尿病。试验于 2014 年 9 月 24 日至 2019 年 3 月 8 日进行。

干预措施

患者随机接受铂类化疗,同时进行胸部放疗(60-63 Gy),联合或不联合巩固化疗,或在放化疗期间和之后接受相同的治疗加二甲双胍,2000mg/d,最多 12 个月。

主要结局和测量指标

主要结局是发生治疗失败事件(即局部疾病进展、远处转移、死亡,以及由于任何原因在 12 个月内停止试验治疗或计划评估)的患者比例。采用双侧 Fisher 精确检验比较比例。采用 Kaplan-Meier 方法估计常规无进展生存期和总生存期。采用通用术语标准 4.03 对不良事件进行分级。所有随机患者均进行意向治疗分析。

结果

由于入组速度较慢,试验提前停止。2014 年至 2019 年期间,共有 54 名患者被随机分配(实验组 26 名,对照组 28 名)。参与者包括 30 名女性(55.6%);平均(SD)年龄为 65.6(7.6)岁。在接受二甲双胍治疗的 18 名患者(69.2%)中,在 1 年内检测到治疗失败,而对照组的 12 名患者(42.9%)(P=0.05)。在实验组,1 年无进展生存率为 34.8%(95%CI,16.6%-53.7%),对照组为 63.0%(95%CI,42.1%-78.1%)(危险比,2.42;95%CI,1.14-5.10)。实验组的总生存率为 47.4%(95%CI,26.3%-65.9%),对照组为 85.2%(95%CI,65.2%-94.2%)(危险比,3.80;95%CI,1.49-9.73)。实验组(53.8%)比对照组(25.0%)更多的患者报告至少有 1 级 3 级或更高的不良事件。

结论和相关性

在这项随机临床试验中,与单纯联合治疗相比,二甲双胍联合放化疗与更差的治疗效果和增加的毒性作用相关。二甲双胍不推荐用于有放化疗适应证的 LA-NSCLC 患者。

试验注册

ClinicalTrials.gov 标识符:NCT02115464。