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

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

Heath Skinner  1 , Chen Hu  2   3 , Theodoros Tsakiridis  4 , Rafael Santana-Davila  5 , Bo Lu  6 , Jeremy J Erasmus  7 , Anthony J Doemer  8 , Gregory M M Videtic  9 , James Coster  10 , Alex Xuezhong Yang  11 , Richard Y Lee  12 , Maria Werner-Wasik  6 , Philip E Schaner  13 , Steven E McCormack  14 , Benjamin T Esparaz  15 , Ronald C McGarry  16 , Jose Bazan  17 , Timothy Struve  18 , Rebecca Paulus  2 , Jeffrey D Bradley  19
Affiliations
Clinical Trial

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

Heath Skinner et al. JAMA Oncol. .

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.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Skinner reported receiving research funding from the National Cancer Institute and National Institute of Dental and Craniofacial Research outside the submitted work and has previously received a grant from the National Cancer Institute for a separate metformin-related clinical trial. Dr Hu reported receiving grants from the National Cancer Institute and the RTOG Foundation and personal fees from Merck & Co outside the submitted work. Dr Tsakiridis reported receiving grants from the Canadian Institutes of Health Research for metformin-related clinical trials; he was the principal investigator of an additional clinical trial with metformin. Dr Tsakiridis also reported receiving grants from Sanofi Canada and fees from AstraZeneca, Sanofi, and AbbVie outside the submitted work. Dr Santana-Davila reported receiving grants and personal fees from Genentech, AbbVie, Lilly, AstraZeneca, and Bayer; personal fees from Bristol Myers Squibb, Ariad, Takeda, NGM Biopharmaceuticals, Cullinan Oncology, and PharmaMar; and grants from Beyond Spring Pharmaceuticals and ISA Pharmaceuticals outside the submitted work. Mr Doemer reported receiving paid consulting (lecturing) for ViewRay, Inc. Dr Werner-Wasik reported receiving grants from the Sidney Kimmel Cancer Center of Thomas Jefferson University to support clinical trial conduct during the conduct of the study. Ms Paulus reported receiving grants from the National Cancer Institute during the conduct of the study. Dr Bradley reported receiving personal fees from AstraZeneca, Mevion Medical Systems, Genentech, and Varian outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. CONSORT Diagram
National Cancer Institute Cancer Therapy Evaluation Program trials randomize patients while eligibility assessment confirmation is ongoing. CT indicates computed tomography; PET, positron emission tomography.
Figure 2.
Figure 2.. Survival Outcomes and Patterns of Recurrence
HR indicates hazard ratio.
See this image and copyright information in PMC

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