Antihyperglycaemic therapies and cancer risk

Stefan Z Lutz1, Harald Staiger2, Andreas Fritsche3

  • 1Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, Department of Internal Medicine, University of Tübingen, Tübingen, Germany German Centre for Diabetes Research (DZD), Tübingen, Germany.

Abstract

Insights

Metformin may protect against certain cancers, while other antidiabetic drugs like sulphonylureas, incretin-based therapies, SGLT2 inhibitors, and pioglitazone may increase cancer risk. Further research is needed to confirm these findings.

Area of Science:

  • Endocrinology
  • Oncology
  • Pharmacology

Background:

  • Antihyperglycemic medications are widely used for diabetes management.
  • Concerns exist regarding the potential impact of these drugs on cancer development and progression.
  • Understanding these effects is crucial for patient safety and treatment optimization.

Purpose of the Study:

  • To review and discuss current evidence on the mitogenic or antimitogenic effects of major antihyperglycemic drug classes.
  • To evaluate the association between antidiabetic medications and malignancies.

Main Methods:

  • Comprehensive literature review of current studies.
  • Analysis of clinical data on antidiabetic drug use and cancer incidence.
  • Evaluation of meta-analyses and controversial findings.

Main Results:

  • Metformin demonstrates protective effects against several site-specific cancers in monotherapy and combination treatments.
  • Concerns regarding increased cancer risk are noted for sulfonylureas, incretin-based therapies (pancreatic, thyroid cancers), SGLT2 inhibitors, and pioglitazone (bladder cancer).
  • Evidence for increased cancer risk with insulin glargine is controversial; alpha-glucosidase inhibitors and glinides show neutral or limited data.

Conclusions:

  • Several antihyperglycemic drug classes may possess mitogenic or tumor-promoting potential, though mechanisms are unclear.
  • Large-scale, randomized clinical trials with long follow-up are essential to definitively assess cancer risks associated with these medications.

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