Division of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN.
Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN.
Hepatology. 2020 Oct;72(4):1298-1309. doi: 10.1002/hep.31146. Epub 2020 Oct 9.
Statins have been proven to be cytotoxic to human cholangiocarcinoma cells by inhibiting cell division and inducing apoptosis. We aimed to determine the effect of statin use on the risk of cancer development and survival in patients with extrahepatic cholangiocarcinoma (ECC), including perihilar cholangiocarcinoma (pCCA) and distal cholangiocarcinoma (dCCA).
A total of 394 patients with ECC and hyperlipidemia who received care at Mayo Clinic Rochester between 2005 and 2015 were matched by age, sex, race, ethnicity, and residency to 788 controls with hyperlipidemia. Clinical and outcome data were abstracted. The odds ratios (ORs) for risk and hazard ratios for outcomes were calculated. The mean age and standard deviation (SD) for cases and controls was 65.6 years (13.8). The number of statin users in cases and controls was 73 (19%) and 403 (51%), respectively. Hepatitis C virus infection (OR, 15.84; 95% confidence interval [CI], 4.06-61.87; P < 0.001) was the most significant risk factor for pCCA followed by inflammatory bowel disease and cirrhosis, whereas other liver disease, including biliary stone disease (OR, 4.06; CI, 2.24-7.36; P < 0.001), was the only significant risk factor for dCCA. Statin use was associated with significantly reduced risk for all ECC (OR, 0.22; CI, 0.16-0.29) as well as for the subtypes pCCA (OR, 0.3; CI, 0.21-0.41) and dCCA (OR, 0.06; CI, 0.03-0.14), all P < 0.0001. Moderate-intensity dosage was found to decrease the risk of ECC (OR, 0.48; CI, 0.34-0.67; P < 0.001). Comparing statin ever users to nonusers, patients with dCCA who used statins had significantly overall better survival (hazard ratio = 0.53; CI, 0.29-0.97; P = 0.04).
This case-control study suggests that statins decrease the risk of ECC and may improve survival in patients with dCCA. Additional validation studies are warranted.
他汀类药物已被证明通过抑制细胞分裂和诱导细胞凋亡对人胆管癌细胞具有细胞毒性。我们旨在确定他汀类药物的使用对包括肝门部胆管癌(pCCA)和远端胆管癌(dCCA)在内的肝外胆管癌(ECC)患者的癌症发展和生存风险的影响。
总共纳入了 2005 年至 2015 年期间在梅奥诊所罗切斯特分院接受治疗的 394 例患有 ECC 和高脂血症的患者,并按年龄、性别、种族、民族和居住地与 788 例高脂血症对照进行了匹配。提取了临床和结局数据。计算了风险的比值比(OR)和结局的风险比。病例和对照组的平均年龄和标准差(SD)分别为 65.6 岁(13.8)。病例组和对照组的他汀类药物使用者分别为 73 名(19%)和 403 名(51%)。丙型肝炎病毒感染(OR,15.84;95%置信区间 [CI],4.06-61.87;P <0.001)是 pCCA 的最重要危险因素,其次是炎症性肠病和肝硬化,而其他肝病,包括胆石病(OR,4.06;CI,2.24-7.36;P <0.001),是唯一的 dCCA 显著危险因素。他汀类药物的使用与所有 ECC(OR,0.22;CI,0.16-0.29)以及 pCCA(OR,0.3;CI,0.21-0.41)和 dCCA(OR,0.06;CI,0.03-0.14)亚型的风险显著降低相关,所有 P <0.0001。发现中等强度剂量可降低 ECC 的风险(OR,0.48;CI,0.34-0.67;P <0.001)。与他汀类药物的既往使用者相比,使用他汀类药物的 dCCA 患者的总体生存情况明显更好(风险比=0.53;CI,0.29-0.97;P =0.04)。
这项病例对照研究表明,他汀类药物可降低 ECC 的风险,并可能改善 dCCA 患者的生存。需要进一步的验证研究。