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


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 Sep 2021
Historique:
pubmed: 30 7 2021
medline: 12 3 2022
entrez: 29 7 2021
Statut: ppublish

Résumé

Non-small cell lung cancer (NSCLC) has relatively poor outcomes. Metformin has significant data supporting its use as an antineoplastic agent. To compare chemoradiation alone vs chemoradiation and metformin in stage III NSCLC. 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. Chemoradiation and consolidation chemotherapy with or without metformin. 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. 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. 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. ClinicalTrials.gov Identifier: NCT02186847.

Identifiants

pubmed: 34323922
pii: 2782111
doi: 10.1001/jamaoncol.2021.2318
pmc: PMC8323052
doi:

Substances chimiques

Metformin 9100L32L2N

Banques de données

ClinicalTrials.gov
['NCT02186847']

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1324-1332

Subventions

Organisme : NCI NIH HHS
ID : U24 CA180803
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA021661
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180822
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189867
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States

Commentaires et corrections

Type : CommentIn

Auteurs

Heath Skinner (H)

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.

Chen Hu (C)

NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania.
Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, Maryland.

Theodoros Tsakiridis (T)

Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton, Ontario, Canada.

Rafael Santana-Davila (R)

Seattle Cancer Care Alliance, Seattle, Washington.

Bo Lu (B)

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

Jeremy J Erasmus (JJ)

MD Anderson Cancer Center, Houston, Texas.

Anthony J Doemer (AJ)

Henry Ford Hospital, Detroit, Michigan.

Gregory M M Videtic (GMM)

Cleveland Clinic, Cleveland, Ohio.

James Coster (J)

University of Kansas Cancer Center, Lawrence.

Alex Xuezhong Yang (AX)

St Francis Cancer Center, Tulsa, Oklahoma.

Richard Y Lee (RY)

The Cancer Center of Hawaii-Liliha, Honolulu.

Maria Werner-Wasik (M)

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

Philip E Schaner (PE)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Steven E McCormack (SE)

Metro-Minnesota Community Oncology Research Consortium, St Louis Park, Minnesota.

Benjamin T Esparaz (BT)

Heartland NCORP, Decatur, Illinois.

Ronald C McGarry (RC)

University of Kentucky/Markey Cancer Center, Lexington.

Jose Bazan (J)

Ohio State University Comprehensive Cancer Center, Columbus.

Timothy Struve (T)

University of Cincinnati/Barrett Cancer Center, Cincinnati, Ohio.

Rebecca Paulus (R)

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

Jeffrey D Bradley (JD)

Emory University, Atlanta, Georgia.

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Classifications MeSH