BMC Medicine (Oct 2022)

Efficacy of metformin therapy in patients with cancer: a meta-analysis of 22 randomised controlled trials

  • Jie Wen,
  • Zhenjie Yi,
  • Yuyao Chen,
  • Jing Huang,
  • Xueyi Mao,
  • Liyang Zhang,
  • Yu Zeng,
  • Quan Cheng,
  • Wenrui Ye,
  • Zhixiong Liu,
  • Fangkun Liu,
  • Jingfang Liu

DOI
https://doi.org/10.1186/s12916-022-02599-4
Journal volume & issue
Vol. 20, no. 1
pp. 1 – 12

Abstract

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Abstract Background To investigate whether metformin monotherapy or adjunctive therapy improves the prognosis in patients with any type of cancer compared to non-metformin users (age ≥18). Methods Databases (Medline, Embase, and the Cochrane Central Register of Controlled Trials) and clinical trial registries ( ClinicalTrials.gov ; the World Health Organization International Clinical Trials Registry Platform) were screened for randomized, controlled trials (RCT) reporting at least progression-free survival (PFS) and/or overall survival (OS). Main outcome measures included hazard ratios (HR), and combined HRs and 95% confidence intervals (CI) were calculated using random-effects models. Results Of the 8419 records screened, 22 RCTs comprising 5943 participants were included. Pooled HRs were not statistically significant in both PFS (HR 0.97, 95% CI 0.82–1.15, I 2 = 50%) and OS (HR 0.98, 95% CI 0.86–1.13, I 2 = 33%) for patients with cancer between the metformin and control groups. Subgroup analyses demonstrated that metformin treatment was associated with a marginally significant improvement in PFS in reproductive system cancers (HR 0.86, 95% CI 0.74–1.00) and a significantly worse PFS in digestive system cancers (HR 1.45, 95% CI 1.03–2.04). The PFS or OS was observed consistently across maintenance dose, diabetes exclusion, median follow-up, risk of bias, and combined antitumoral therapies. Conclusion Metformin treatment was not associated with cancer-related mortality in adults compared with placebo or no treatment. However, metformin implied beneficial effects in the PFS of the patients with reproductive system cancers but was related to a worse PFS in digestive system cancers. Systematic review registration PROSPERO registration number CRD42022324672.

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