Too good to be true: Are GLP-1 receptor agonists the new metformin?

J Diabetes Complications. 2024 Oct;38(10):108851. doi: 10.1016/j.jdiacomp.2024.108851. Epub 2024 Aug 30.

Abstract

Recently, a health-care database study showed that persons with type 2 diabetes taking GLP-1 receptor agonists (GLP-1 RA) had a significantly lower risk of 10 out of 13 obesity-related cancers than patients taking insulin (Wang L, et al. JAMA Netw Open. 2024 7: e2421305). For some cancers, hazard ratios <0.5 were reported. This is reminiscent of studies published >10 years ago showing that people with type 2 diabetes taking metformin had a lower risk of many types of cancer than those not taking metformin. In some studies, also risk reductions of >50 % were reported. The strong effects observed in the metformin studies were explained by time-related biases, in particular, immortal time bias. In the current GLP-1 RA study, it was striking that the curves for the cumulative incidence of several cancers in GLP-1 RA and insulin users diverged immediately after therapy onset. This indicates that there is most likely a time-related bias: insulin is given at much later stages of type 2 diabetes than GLP-1 RA. The current study suggests that one should be sceptical about database results when spectacular risk reductions are reported. Time-related bias should always be considered as an alternative explanation.

Keywords: Cancer; Diabetes mellitus; Glucagon-like peptide-1 receptor agonist; Immortal time bias; Metformin; Time-lag bias.

MeSH terms

  • Bias
  • Diabetes Mellitus, Type 2* / complications
  • Diabetes Mellitus, Type 2* / drug therapy
  • Diabetes Mellitus, Type 2* / epidemiology
  • Glucagon-Like Peptide-1 Receptor Agonists
  • Glucagon-Like Peptide-1 Receptor* / agonists
  • Humans
  • Hypoglycemic Agents* / therapeutic use
  • Incidence
  • Insulin / therapeutic use
  • Metformin* / therapeutic use
  • Neoplasms* / epidemiology

Substances

  • Glucagon-Like Peptide-1 Receptor
  • Metformin
  • Hypoglycemic Agents
  • Insulin
  • Glucagon-Like Peptide-1 Receptor Agonists