Endocrine oncology

Glucagon‐like peptide‐1 receptor agonists and risk of thyroid cancer: A systematic review and meta‐analysis of randomized controlled trials

Diabetes Obes MetabPublished Systematic review and meta-analysis of randomised trials

Pooled result · Overall thyroid cancerResult — go to the resultMH-OR 1.52 95% CI 1.01–2.29

Authors' conclusion

Our meta-analysis showed that GLP-1RA treatment could be associated with a moderate increase in relative risk for thyroid cancer in clinical trials, with a small increase in absolute risk. Studies of longer duration are required to assess the clinical implications of this finding.

Study context

Population
Randomized clinical trials (RCTs) comparing a GLP-1 RA with any comparator, lasting ≥52 weeks, reporting adverse events independently of principal endpoint and population64 trials
Comparison
GLP-1 RA vs any comparator
Outcome
Overall thyroid cancer
Methodological detailsRCTs lasting at least 52 weeks
  • RCTs lasting at least 52 weeks

Pooled result

As reported in the abstract

MH-OR

1.52

95% CI 1.01–2.29

P = 0.04

GLP-1RAvs Comparator
MH-OR 1.52 (95% CI 1.01–2.29); P = 0.04
Fragility index
1
5-year NNH
1349

Further pooled results

Overall thyroid cancer, trials lasting ≥104 weeks

Association remained significant: MH-OR (95% CI 1.00, 3.12); P = 0.05
1.76

Papillary thyroid cancer

No significant association: MH-OR (95% CI 0.77, 3.06); P = 0.22
1.54

Medullary thyroid cancer

No significant association: MH-OR (95% CI 0.23, 9.16); P = 0.55
1.44

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Glucagon‐like peptide‐1 receptor agonists and risk of thyroid cancer: A systematic review and meta‐analysis of randomized controlled trials. Diabetes Obes Metab. Published 29 November 2023. doi:10.1111/dom.15382

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.