GLP-1药物与结肠癌患者死亡率显著降低相关联。
GLP-1 drugs linked to lower death rates in colon cancer patients

原始链接: https://today.ucsd.edu/story/glp-1-drugs-linked-to-dramatically-lower-death-rates-in-colon-cancer-patients

最近加州大学圣地亚哥分校的一项研究表明,GLP-1受体激动剂——例如Ozempic、Wegovy和Mounjaro等药物——可能显著提高结肠癌患者的生存率。研究人员分析了超过6800名患者的数据,发现服用GLP-1药物的患者五年内死亡的可能性低于未服用该药物的患者(分别为15.5%和37.1%)。 即使在考虑年龄、BMI和疾病严重程度等因素后,这种益处仍然显著,尤其是在BMI超过35的患者中。研究人员认为这可能是由于这些药物能够减轻炎症、改善胰岛素敏感性并促进体重减轻——所有这些因素都会影响癌症进展。实验室研究也暗示了其直接的抗癌作用。 虽然是观察性研究,但这些发现强调了迫切需要进行临床试验,以确认GLP-1药物是否可以直接改善癌症生存率,尤其是在与肥胖相关的病例中。该研究发表于2025年11月11日的《Cancer Investigation》。

## GLP-1药物与结肠癌生存率 一项最新观察性研究将GLP-1药物的使用(如Ozempic和Wegovy)与结肠癌患者较低的死亡率联系起来。 即使在调整了BMI和疾病严重程度等因素后,该研究也显示出显著的相关性,但研究人员强调需要进一步调查以确定这是否是直接的抗癌作用,或是体重减轻和代谢健康改善的间接结果。 讨论的重点在于,益处是否主要来自体重减轻,因为GLP-1药物通常会导致食欲降低和代谢功能增强。 一些评论员指出,有证据表明GLP-1药物具有独立于体重减轻的心脏保护和潜在的抗衰老作用,而另一些人则强调了关于改善物质使用控制的零星报告。 潜在的副作用和药物高昂的成本也引起了担忧,一些人认为益处大于风险,类似于疫苗。 讨论还涉及仿制药未来上市后,潜在的可负担性提高。
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原文

A new University of California San Diego study offers compelling evidence that GLP-1 receptor agonists — the class of drugs behind Ozempic, Wegovy and Mounjaro, for example — may do more than regulate blood sugar and weight. In an analysis of more than 6,800 colon cancer patients across all University of California Health sites, researchers found that those taking glucagon-like peptide-1 (GLP-1) medications were less than half as likely to die within five years compared to those who weren’t on the drugs (15.5% vs. 37.1%).

The study, led by Raphael Cuomo, Ph.D., associate professor in the Department of Anesthesiology at UC San Diego School of Medicine and member of UC San Diego Moores Cancer Center, used real-world clinical data from the University of California Health Data Warehouse to assess outcomes across the state’s academic medical centers. After adjusting for age, body mass index (BMI), disease severity and other health factors, GLP-1 users still showed significantly lower odds of death, suggesting a strong and independent protective effect.

The survival benefit appeared most pronounced in patients with very high BMI (over 35), hinting that GLP-1 drugs may help counteract the inflammatory and metabolic conditions that worsen colon cancer prognosis. Researchers believe several biological mechanisms could explain the link. Beyond regulating blood sugar, GLP-1 receptor agonists reduce systemic inflammation, improve insulin sensitivity and promote weight loss — all factors that can dampen tumor-promoting pathways. Laboratory studies also suggest that GLP-1 drugs may directly prevent cancer cell growth, trigger cancer cell death and reshape the tumor microenvironment. However, the study authors emphasize that more research is needed to confirm these mechanisms and determine whether the survival benefit observed in this real-world analysis represents a direct anti-cancer effect or an indirect result of improved metabolic health.

Cuomo notes that while these results are observational, they underscore an urgent need for clinical trials to test whether GLP-1 drugs can improve cancer survival rates, especially for patients with obesity-related cancers.

The study appeared in Cancer Investigation on Nov. 11, 2025.

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