他汀类药物、阿司匹林和二甲双胍的使用与肝移植后肝细胞癌相关结果的风险:一项回顾性研究。

William Chung, Kevin Wong, Noel Ravindranayagam, Lauren Tang, Josephine Grace, Darren Wong, Danny Con, Marie Sinclair, Avik Majumdar, Numan Kutaiba, Samuel Hui, Paul Gow, Vijayaragavan Muralidharan, Alexander Dobrovic, Adam Testro
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Sensitivity analysis was performed to account for immortality time bias and statin dosing.</p><p><strong>Results: </strong>Three hundred and five patients were included in this study, with 253 (82.95%) males with a median age of 58.90 years. Aetiologies of liver disease were 150 (49.18%) hepatitis C, 73 (23.93%) hepatitis B (HBV) and 33 (10.82%) non-alcoholic fatty liver disease (NAFLD). 56 (18.36%) took statins, 51 (16.72%) aspirin and 50 (16.39%) metformin. During a median follow-up time of 59.90 months, 34 (11.15%) developed HCC-recurrence, 48 (15.74%) died, 17 (5.57%) from HCC-related mortality. 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引用次数: 0

摘要

背景:肝移植(LT)是肝细胞癌(HCC)患者的一种潜在治愈疗法。肝移植后HCC复发与生存率降低有关。目的:研究使用具有化学预防HCC作用的药物是否对LT后患者的预后有益:这是一项回顾性研究,研究对象是2005-2022年期间在澳大利亚一家中心接受过死神捐献LT治疗HCC的成年患者。在LT术后24个月内,他汀类药物、阿司匹林或二甲双胍的使用时间≥29天。生存分析采用了具有时间依赖性协变量的考克斯比例危险模型。结果指标为HCC复发与全因死亡率、HCC复发与HCC相关死亡率的复合终点。进行了敏感性分析,以考虑不死时间偏差和他汀类药物剂量:本研究共纳入 355 例患者,其中 253 例(82.95%)为男性,中位年龄为 58.90 岁。肝病病因包括 150 例(49.18%)丙型肝炎、73 例(23.93%)乙型肝炎(HBV)和 33 例(10.82%)非酒精性脂肪肝(NAFLD)。56人(18.36%)服用他汀类药物,51人(16.72%)服用阿司匹林,50人(16.39%)服用二甲双胍。中位随访时间为 59.90 个月,其中 34 人(11.15%)出现 HCC 复发,48 人(15.74%)死亡,17 人(5.57%)死于 HCC 相关死亡。他汀类药物、阿司匹林或二甲双胍的使用与 HCC 复发或全因死亡率的复合终点差异无统计学意义[危险比 (HR):1.16,95%CI:0.58-2.30;HR:1.21,95%CI:0.28-5.27;HR:0.61,95%CI:0.27-1.36]、HCC-复发(HR:0.52,95%CI:0.20-1.35;HR:0.51,95%CI:0.14-1.93;HR 1.00,95%CI:0.37-2.72)或HCC相关死亡率(HR:0.32,95%CI:0.033-3.09;HR:0.71,95%CI:0.14-3.73;HR:1.57,95%CI:0.61-4.04)。他汀类药物的剂量与HCC相关结果的统计学差异无关:结论:在非酒精性脂肪肝比例较低的澳大利亚患者队列中,他汀类药物、二甲双胍或阿司匹林的使用与LT后HCC相关结果的改善无关。需要进一步开展前瞻性多中心研究,以明确这些药物对改善HCC相关预后的潜在益处。
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Statin, aspirin and metformin use and risk of hepatocellular carcinoma related outcomes following liver transplantation: A retrospective study.

Background: Liver transplantation (LT) is a potentially curative therapy for patients with hepatocellular carcinoma (HCC). HCC-recurrence following LT is associated with reduced survival. There is increasing interest in chemoprophylaxis to improve HCC-related outcomes post-LT.

Aim: To investigate whether there is any benefit for the use of drugs with proposed chemoprophylactic properties against HCC, and patient outcomes following LT.

Methods: This was a retrospective study of adult patients who received Deceased Donor LT for HCC from 2005-2022, from a single Australian centre. Drug use was defined as statin, aspirin or metformin therapy for ≥ 29 days, within 24 months post-LT. A cox proportional-hazards model with time-dependent covariates was used for survival analysis. Outcome measures were the composite-endpoint of HCC-recurrence and all-cause mortality, HCC-recurrence and HCC-related mortality. Sensitivity analysis was performed to account for immortality time bias and statin dosing.

Results: Three hundred and five patients were included in this study, with 253 (82.95%) males with a median age of 58.90 years. Aetiologies of liver disease were 150 (49.18%) hepatitis C, 73 (23.93%) hepatitis B (HBV) and 33 (10.82%) non-alcoholic fatty liver disease (NAFLD). 56 (18.36%) took statins, 51 (16.72%) aspirin and 50 (16.39%) metformin. During a median follow-up time of 59.90 months, 34 (11.15%) developed HCC-recurrence, 48 (15.74%) died, 17 (5.57%) from HCC-related mortality. Statin, aspirin or metformin use was not associated with statistically significant differences in the composite endpoint of HCC-recurrence or all-cause mortality [hazard ratio (HR): 1.16, 95%CI: 0.58-2.30; HR: 1.21, 95%CI: 0.28-5.27; HR: 0.61, 95%CI: 0.27-1.36], HCC-recurrence (HR: 0.52, 95%CI: 0.20-1.35; HR: 0.51, 95%CI: 0.14-1.93; HR 1.00, 95%CI: 0.37-2.72), or HCC-related mortality (HR: 0.32, 95%CI: 0.033-3.09; HR: 0.71, 95%CI: 0.14-3.73; HR: 1.57, 95%CI: 0.61-4.04) respectively. Statin dosing was not associated with statistically significant differences in HCC-related outcomes.

Conclusion: Statin, metformin or aspirin use was not associated with improved HCC-related outcomes post-LT, in a largely historical cohort of Australian patients with a low proportion of NAFLD. Further prospective, multicentre studies are required to clarify any potential benefit of these drugs to improve HCC-related outcomes.

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