Literature DB >> 31486833

Effect of Metformin Plus Tyrosine Kinase Inhibitors Compared With Tyrosine Kinase Inhibitors Alone in Patients With Epidermal Growth Factor Receptor-Mutated Lung Adenocarcinoma: A Phase 2 Randomized Clinical Trial.

Oscar Arrieta1, Feliciano Barrón1, Miguel-Ángel Salinas Padilla1, Alejandro Avilés-Salas1, Laura Alejandra Ramírez-Tirado1, Manuel Jesús Arguelles Jiménez1, Edgar Vergara1, Zyanya Lucia Zatarain-Barrón1, Norma Hernández-Pedro1, Andrés F Cardona2,3,4, Graciela Cruz-Rico1, Pedro Barrios-Bernal1, Masao Yamamoto Ramos5, Rafael Rosell6.   

Abstract

IMPORTANCE: Metformin hydrochloride is emerging as a repurposed anticancer drug. Preclinical and retrospective studies have shown that it improves outcomes across a wide variety of neoplasms, including lung cancer. Particularly, evidence is accumulating regarding the synergistic association between metformin and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs).
OBJECTIVE: To assess the progression-free survival (PFS) in patients with advanced lung adenocarcinoma who received treatment with EGFR-TKIs plus metformin compared with those who received EGFR-TKIs alone. DESIGN, SETTING, AND PARTICIPANTS: Open-label, randomized, phase 2 trial conducted at the Instituto Nacional de Cancerología (INCan), Mexico City, Mexico. Eligible patients were 18 years or older, had histologically confirmed stage IIIB-IV lung adenocarcinoma with an activating EGFR mutation.
INTERVENTIONS: Patients were randomly allocated to receive EGFR-TKIs (erlotinib hydrochloride, afatinib dimaleate, or gefitinib at standard dosage) plus metformin hydrochloride (500 mg twice a day) or EGFR-TKIs alone. Treatment was continued until occurrence of intolerable toxic effects or withdrawal of consent. MAIN OUTCOMES AND MEASURES: The primary outcome was PFS in the intent-to-treat population. Secondary outcomes included objective response rate, disease control rate, overall survival (OS), and safety.
RESULTS: Between March 31, 2016, and December 31, 2017, a total of 139 patients (mean [SD] age, 59.4 [12.0] years; 65.5% female) were randomly assigned to receive EGFR-TKIs (n = 70) or EGFR-TKIs plus metformin (n = 69). The median PFS was significantly longer in the EGFR-TKIs plus metformin group (13.1; 95% CI, 9.8-16.3 months) compared with the EGFR-TKIs group (9.9; 95% CI, 7.5-12.2 months) (hazard ratio, 0.60; 95% CI, 0.40-0.94; P = .03). The median OS was also significantly longer for patients receiving the combination therapy (31.7; 95% CI, 20.5-42.8 vs 17.5; 95% CI, 11.4-23.7 months; P = .02). CONCLUSIONS AND RELEVANCE: To our knowledge, this is the first study to prospectively show that the addition of metformin to standard EGFR-TKIs therapy in patients with advanced lung adenocarcinoma significantly improves PFS. These results justify the design of a phase 3, placebo-controlled study. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT03071705.

Entities:  

Year:  2019        PMID: 31486833      PMCID: PMC6735425          DOI: 10.1001/jamaoncol.2019.2553

Source DB:  PubMed          Journal:  JAMA Oncol        ISSN: 2374-2437            Impact factor:   31.777


  48 in total

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Review 2.  Mitochondrial Metabolism as a Target for Cancer Therapy.

Authors:  Karthik Vasan; Marie Werner; Navdeep S Chandel
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Review 3.  The role of metformin on lung cancer survival: the first systematic review and meta-analysis of observational studies and randomized clinical trials.

Authors:  Tatiana Natasha Toporcov; Elisabete Weiderpass; Suzan Brancher; Ana Elisa Ribeiro
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4.  Mesothelial Cell HIF1α Expression Is Metabolically Downregulated by Metformin to Prevent Oncogenic Tumor-Stromal Crosstalk.

Authors:  Peter C Hart; Hilary A Kenny; Niklas Grassl; Karen M Watters; Lacey M Litchfield; Fabian Coscia; Ivana Blaženović; Lisa Ploetzky; Oliver Fiehn; Matthias Mann; Ernst Lengyel; Iris L Romero
Journal:  Cell Rep       Date:  2019-12-17       Impact factor: 9.423

Review 5.  X- and Y-Linked Chromatin-Modifying Genes as Regulators of Sex-Specific Cancer Incidence and Prognosis.

Authors:  Rossella Tricarico; Emmanuelle Nicolas; Michael J Hall; Erica A Golemis
Journal:  Clin Cancer Res       Date:  2020-07-30       Impact factor: 12.531

Review 6.  Lessons from Cancer Metabolism for Pulmonary Arterial Hypertension and Fibrosis.

Authors:  SeungHye Han; Navdeep S Chandel
Journal:  Am J Respir Cell Mol Biol       Date:  2021-08       Impact factor: 6.914

Review 7.  Targeting cancer-promoting inflammation - have anti-inflammatory therapies come of age?

Authors:  Jiajie Hou; Michael Karin; Beicheng Sun
Journal:  Nat Rev Clin Oncol       Date:  2021-01-19       Impact factor: 66.675

Review 8.  Shining a light on metabolic vulnerabilities in non-small cell lung cancer.

Authors:  Catríona M Dowling; Hua Zhang; Tríona Ní Chonghaile; Kwok-Kin Wong
Journal:  Biochim Biophys Acta Rev Cancer       Date:  2020-10-29       Impact factor: 10.680

9.  Does metformin improve the efficacy of standard epidermal growth factor receptor-tyrosine kinase inhibitor treatment for patients with advanced non-small-cell lung cancer?

Authors:  Zhangyu Lin; Guangchen Li; Xinyu Xu; Jiandong Mei
Journal:  Interact Cardiovasc Thorac Surg       Date:  2021-01-01

10.  Circulating Insulin-Like Growth Factor-1 and Risk of Total and 19 Site-Specific Cancers: Cohort Study Analyses from the UK Biobank.

Authors:  Frank Qian; Dezheng Huo
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2020-08-20       Impact factor: 4.254

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