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

IF 3.9 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrinology and Metabolism Pub Date : 2025-01-15 DOI:10.3803/EnM.2024.2164
A B M Kamrul-Hasan, Muhammad Shah Alam, Deep Dutta, Thanikai Sasikanth, Fatema Tuz Zahura Aalpona, Lakshmi Nagendra
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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.

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替西帕肽与糖尿病患者和非糖尿病患者的癌症风险:一项系统综述和荟萃分析。
背景:来自随机对照试验(rct)的关于替西帕肽致癌潜力的数据有限。此外,没有荟萃分析纳入所有相关的随机对照试验来评估与替西肽相关的癌症风险。方法:通过电子数据库检索涉及干预组接受替西帕肽治疗的患者和对照组接受安慰剂或任何活性比较物治疗的患者的随机对照试验。主要结果是任何癌症的总体风险,次要结果是替西帕肽组与对照组中特定类型癌症的风险。结果:13项随机对照试验共13761名受试者进行了分析。在26至72周内,替西肽组和合并对照组患任何癌症的风险相同(风险比,0.78;95%置信区间为0.53 ~ 1.16;P = 0.22)。两组糖尿病患者和非糖尿病患者患癌症的风险相当。在亚组分析中,替西帕肽与安慰剂、胰岛素和胰高血糖素样肽-1受体激动剂组的风险也相似。与对照组相比,不同剂量的替西帕肽的总体癌症风险也相当;只有10mg剂量的替西帕肽比安慰剂有更低的癌症风险。此外,与对照组(合并或单独)相比,替西帕肽没有增加任何特定癌症类型的风险。尽管10-和15-mg替西帕肽组的血清降钙素比安慰剂组有更大的增加,但纳入的随机对照试验未报告甲状腺乳头状癌病例。结论:在26 - 72周的随机对照试验中使用替西帕肽不会增加总体或特定的癌症风险。
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来源期刊
Endocrinology and Metabolism
Endocrinology and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
6.60
自引率
5.90%
发文量
145
审稿时长
24 weeks
期刊介绍: The aim of this journal is to set high standards of medical care by providing a forum for discussion for basic, clinical, and translational researchers and clinicians on new findings in the fields of endocrinology and metabolism. Endocrinology and Metabolism reports new findings and developments in all aspects of endocrinology and metabolism. The topics covered by this journal include bone and mineral metabolism, cytokines, developmental endocrinology, diagnostic endocrinology, endocrine research, dyslipidemia, endocrine regulation, genetic endocrinology, growth factors, hormone receptors, hormone action and regulation, management of endocrine diseases, clinical trials, epidemiology, molecular endocrinology, neuroendocrinology, neuropeptides, neurotransmitters, obesity, pediatric endocrinology, reproductive endocrinology, signal transduction, the anatomy and physiology of endocrine organs (i.e., the pituitary, thyroid, parathyroid, and adrenal glands, and the gonads), and endocrine diseases (diabetes, nutrition, osteoporosis, etc.).
期刊最新文献
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