Krishnan Arunkumar, Schneider Carolin V, Arkenau Hendrik-Tobias, Mauro Ezequiel Matias, Forner Alejandro, Scott Butsch W, Walsh Declan, Alqahtani Saleh A
Department of Supportive Oncology, Atrium Health Levine Cancer, Charlotte, NC, USA.
Department of Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
J Clin Transl Endocrinol. 2024 Sep 18;38:100370. doi: 10.1016/j.jcte.2024.100370. eCollection 2024 Dec.
To examine the association between the use of incretin-based drugs [glucagon-like peptide-1 receptor agonists (GLP-1RAs), dipeptidyl peptidase-4 inhibitors (DPP-4Is)] and the risk of cholangiocarcinoma (CCA) in the United States.
This large population-based, retrospective cohort study using the TriNetX datasets included adult patients with type 2 diabetes mellitus (T2DM) who were new users of GLP-1RAs, DPP-4Is, or other second- or third-line antidiabetic drugs between 2010 and 2021. The primary outcome was the incidence of CCA.
A total of 3,816,071 patients were included (mean age, 61.4 years, female, 49.3 %). A 51 % and 23 % risk reduction in CCA after 1 year of exposure to GLP-1RAs (hazard ratio 0.49; 95 % CI 0.40-0.60) and DPP4Is (0.77, 95 % CI 0.67-0.90), respectively compared to new second-or third-line users. Results were consistent at 3, 5, and 7 years of follow-up (0.66, 0.71, and 0.72 for GLP-1RAs and 0.84, 0.87, and 0.85 for DPP-4Is, respectively). Compared to new metformin users, GLP-1RA users were associated with a 42 % lower risk of developing CCA, whereas DPP-4I group was not associated with an increased risk.
GLP-1RAs and DPP-4Is were not associated with a significantly increased risk of CCA. GLP-1RAs even showed a reduced risk of CCA development. They can be considered as safe and effective treatment options for patients with T2DM at risk of CCA.
研究在美国使用基于肠促胰岛素的药物[胰高血糖素样肽-1受体激动剂(GLP-1RAs)、二肽基肽酶-4抑制剂(DPP-4Is)]与胆管癌(CCA)风险之间的关联。
这项基于人群的大型回顾性队列研究使用TriNetX数据集,纳入了2010年至2021年间新使用GLP-1RAs、DPP-4Is或其他二线或三线抗糖尿病药物的2型糖尿病(T2DM)成年患者。主要结局是CCA的发病率。
共纳入3816071例患者(平均年龄61.4岁,女性占49.3%)。与新使用二线或三线药物的患者相比,使用GLP-1RAs(风险比0.49;95%置信区间0.40-0.60)和DPP-4Is(0.77,95%置信区间0.67-0.90)1年后,CCA风险分别降低了51%和23%。在3年、5年和7年的随访中结果一致(GLP-1RAs分别为0.66,0.71和0.72,DPP-4Is分别为0.84,0.87和0.85)。与新使用二甲双胍的患者相比,使用GLP-1RAs的患者发生CCA的风险降低42%,而DPP-4I组与风险增加无关。
GLP-1RAs和DPP-4Is与CCA风险显著增加无关。GLP-1RAs甚至显示出降低CCA发生风险的作用。对于有CCA风险的T2DM患者,它们可被视为安全有效的治疗选择。