» Articles » PMID: 32118712

Aspirin and the Risk of Hepatocellular Carcinoma Development in Patients with Alcoholic Cirrhosis

Overview
Specialty General Medicine
Date 2020 Mar 3
PMID 32118712
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Aspirin therapy has shown protective effects against hepatocellular carcinoma (HCC) in preclinical studies. However, it is unclear whether aspirin therapy lowers the risk of HCC in patients with alcoholic cirrhosis.A retrospective analysis of data from 949 consecutive patients with alcoholic cirrhosis who abstained from alcoholic drinking was performed. The primary and secondary outcomes were development of HCC and gastrointestinal bleeding events, respectively. Risk was compared between patients with aspirin treatment and patients who were not treated (non-aspirin group) using a time-varying Cox proportional hazards model for total population and propensity score-matching analysis.The aspirin group included 224 patients and the non-aspirin group had 725 patients. During the study period of median duration of 3.1 years, 133 patients (13.6%) developed HCC. In time-varying Cox proportional analyses, the aspirin group showed a significantly lower risk of HCC (adjusted hazard ratio [aHR]: 0.13; 95% confidence interval [CI]: 0.08-0.21; P < .001). In propensity score-matched pairs, aspirin therapy significantly reduced the risk of HCC (aHR: 0.14; 95% CI: 0.09-0.22; P < .001). In bleeding risk, treatment with aspirin alone was not significantly associated with a higher bleeding risk (aHR: 0.81; 95% CI: 0.45-1.44; P = .46).Aspirin therapy was associated with the lower risk of HCC in patients with alcoholic cirrhosis.

Citing Articles

Current and emerging strategies for the prevention of hepatocellular carcinoma.

Yeo Y, Abdelmalek M, Khan S, Moylan C, Rodriquez L, Villanueva A Nat Rev Gastroenterol Hepatol. 2024; 22(3):173-190.

PMID: 39653784 DOI: 10.1038/s41575-024-01021-z.


Prognostic impact of aspirin in patients with hepatocellular carcinoma after liver resection: propensity-score-matched analysis.

Matsumoto T, Kitano Y, Imai K, Ogawa D, Yumoto S, Takematsu T Int J Clin Oncol. 2024; 30(1):92-98.

PMID: 39438421 DOI: 10.1007/s10147-024-02646-5.


Association between antithrombotic agents use and hepatocellular carcinoma risk: a two-sample mendelian randomization analysis.

Yang F, Li O, Gao B, Chen Z, Li B, He J J Cancer Res Clin Oncol. 2024; 150(10):470.

PMID: 39436427 PMC: 11496351. DOI: 10.1007/s00432-024-05960-7.


Postoperative adjuvant aspirin for patients with hepatitis B virus-related hepatocellular carcinoma and portal vein tumor thrombus: An open-label, randomized controlled trial.

Lu C, Jiang Y, Feng J, Wang L, Wei X, Zhou B Heliyon. 2023; 9(9):e20015.

PMID: 37810112 PMC: 10559736. DOI: 10.1016/j.heliyon.2023.e20015.


The Effect of Aspirin Use on Incident Hepatocellular Carcinoma-An Updated Systematic Review and Meta-Analysis.

Abdelmalak J, Tan N, Con D, Eslick G, Majeed A, Kemp W Cancers (Basel). 2023; 15(13).

PMID: 37444628 PMC: 10341252. DOI: 10.3390/cancers15133518.


References
1.
Maini M, Schurich A . Platelets harness the immune response to drive liver cancer. Proc Natl Acad Sci U S A. 2012; 109(32):12840-1. PMC: 3420167. DOI: 10.1073/pnas.1210296109. View

2.
Gao B, Bataller R . Alcoholic liver disease: pathogenesis and new therapeutic targets. Gastroenterology. 2011; 141(5):1572-85. PMC: 3214974. DOI: 10.1053/j.gastro.2011.09.002. View

3.
Tarantino G, Citro V, Conca P, Riccio A, Tarantino M, Capone D . What are the implications of the spontaneous spleno-renal shunts in liver cirrhosis?. BMC Gastroenterol. 2009; 9:89. PMC: 2785828. DOI: 10.1186/1471-230X-9-89. View

4.
Fujiwara N, Singal A, Hoshida Y . Dose and Duration of Aspirin Use to Reduce Incident Hepatocellular Carcinoma. Hepatology. 2019; 70(6):2216-2217. PMC: 6885093. DOI: 10.1002/hep.30813. View

5.
Sitia G, Aiolfi R, Di Lucia P, Mainetti M, Fiocchi A, Mingozzi F . Antiplatelet therapy prevents hepatocellular carcinoma and improves survival in a mouse model of chronic hepatitis B. Proc Natl Acad Sci U S A. 2012; 109(32):E2165-72. PMC: 3420192. DOI: 10.1073/pnas.1209182109. View