Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia; Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Australia.
Gynecol Oncol. 2021 Jun;161(3):858-863. doi: 10.1016/j.ygyno.2021.04.001. Epub 2021 Apr 10.
A recent paper suggested all women with endometrial cancer should take statins but it is unclear whether there is sufficient evidence to justify this recommendation.
We identified all women diagnosed with uterine cancer in Australia between July 2003 and December 2013 (2012 in New South Wales) through the Australian Cancer Database (N = 16,501) and linked these to the national prescription database and National Death Index to identify statin use and survival outcomes to December 2015. We used Cox proportional hazards regression to estimate hazard ratios (HR) and 95% confidence intervals (CI) for the associations between statin use and survival.
Among the 15,703 women with endometrial cancer, pre-diagnosis statin use was not associated with survival. Endometrial cancer-specific mortality was lower among women who used statins after diagnosis (time-varying models: HR = 0.92; 95%CI 0.82-1.03) but the association was only seen among women with type 1 cancers (0.87; 0.76-1.00), for hydrophilic statins (0.84; 0.68-1.03) and for new use of statins after diagnosis (0.75; 0.59-0.95). There was a weak dose-response with increasing number of statin prescriptions. Sensitivity analyses using inverse probability of treatment weights were similar.
Women with endometrial cancer who take statins after diagnosis may have better survival than those who do not use statins. However, it is impossible to completely rule out bias, particularly reverse causation where disease status may affect statin use. We believe it is too early to recommend all women with endometrial cancer take statins, but there is sufficient evidence to justify a randomized trial.
最近的一篇论文提出,所有子宫内膜癌患者都应服用他汀类药物,但尚不清楚这一建议是否有足够的证据支持。
我们通过澳大利亚癌症数据库(Australian Cancer Database)确定了 2003 年 7 月至 2013 年 12 月(2012 年在新南威尔士州)期间澳大利亚所有被诊断患有子宫癌的女性(N=16501),并将这些患者与国家处方数据库和国家死亡索引相关联,以确定他汀类药物的使用情况和截至 2015 年 12 月的生存结果。我们使用 Cox 比例风险回归估计了他汀类药物使用与生存之间的关联的风险比(HR)和 95%置信区间(CI)。
在 15703 名患有子宫内膜癌的女性中,诊断前使用他汀类药物与生存无关。在诊断后使用他汀类药物的女性中,子宫内膜癌特异性死亡率较低(时间变化模型:HR=0.92;95%CI 0.82-1.03),但这种关联仅见于 1 型癌症患者(0.87;0.76-1.00)、亲水性他汀类药物(0.84;0.68-1.03)和诊断后开始使用新的他汀类药物(0.75;0.59-0.95)。随着他汀类药物处方数量的增加,存在微弱的剂量反应关系。使用治疗反概率加权的敏感性分析结果相似。
诊断后服用他汀类药物的子宫内膜癌患者的生存可能优于未服用他汀类药物的患者。然而,完全排除偏倚是不可能的,特别是在疾病状况可能影响他汀类药物使用的反向因果关系中。我们认为,现在建议所有子宫内膜癌患者服用他汀类药物还为时过早,但有足够的证据支持进行随机试验。