Endocrinol Metab.  2025 Feb;40(1):112-124. 10.3803/EnM.2024.2164.

Tirzepatide and Cancer Risk in Individuals with and without Diabetes: A Systematic Review and Meta-Analysis

Affiliations
  • 1Department of Endocrinology, Mymensingh Medical College, Mymensingh, Bangladesh
  • 2Department of Medicine, Army Medical College Cumilla, Cumilla, Bangladesh
  • 3Department of Endocrinology, CEDAR Superspeciality Clinics, New Delhi, India
  • 4Department of Endocrinology, National Hospital of Sri Lanka, Colombo, Sri Lanka
  • 5Department of Obstetrics and Gynecology, Atpara Upazila Health Complex, Netrokona, Bangladesh
  • 6Department of Endocrinology, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India

Abstract

Background
Data on the carcinogenic potential of tirzepatide from randomized controlled trials (RCTs) are limited. Furthermore, no meta-analysis has included all relevant RCTs to assess the cancer risk associated with tirzepatide.
Methods
RCTs involving patients receiving tirzepatide in the intervention arm and either a placebo or any active comparator in the control arm were searched through electronic databases. The primary outcome was the overall risk of any cancer, and secondary outcomes were the risks of specific types of cancer in the tirzepatide versus the control groups.
Results
Thirteen RCTs with 13,761 participants were analyzed. Over 26 to 72 weeks, the tirzepatide and pooled control groups had identical risks of any cancer (risk ratio, 0.78; 95% confidence interval, 0.53 to 1.16; P=0.22). The two groups had comparable cancer risks in patients with and without diabetes. In subgroup analyses, the risks were also similar in the tirzepatide versus placebo, insulin, and glucagon-like peptide-1 receptor agonist groups. The overall cancer risk was also comparable for different doses of tirzepatide compared to the control groups; only a 10-mg tirzepatide dose had a lower risk of any cancer than placebo. Furthermore, compared to the control groups (pooled or separately), tirzepatide did not increase the risk of any specific cancer types. Despite greater increments in serum calcitonin with 10- and 15-mg tirzepatide doses than with placebo, the included RCTs reported no cases of papillary thyroid carcinoma.
Conclusion
Tirzepatide use in RCTs over 26 to 72 weeks did not increase overall or specific cancer risk.

Keyword

Tirzepatide; Meta-analysis; Diabetes mellitus, type 2; Obesity; Neoplasms; Thyroid neoplasms; Pancreatic neoplasms

Figure

  • Fig. 1. Flowchart on study retrieval and inclusion in the meta-analysis.

  • Fig. 2. Forest plot highlighting the risk of any cancer in the tirzepatide versus pooled control groups. IV, intravenous; CI, confidence interval.


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