Daily Aspirin Reduced the Incidence of Hepatocellular Carcinoma and Overall Mortality in Patients with Cirrhosis

Cirrhosis is the primary risk factor for hepatocellular carcinoma (HCC) and gastrointestinal bleeding (GI). We aimed to assess the efficacy and safety of daily aspirin on HCC occurrence, overall survival, and GI bleeding in cirrhotic patients. A total of 35,898 eligible cases were enrolled for analy...

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Veröffentlicht in:Cancers 2023-05, Vol.15 (11), p.2946
Hauptverfasser: Lee, Chern-Horng, Hsu, Chiu-Yi, Yen, Tzung-Hai, Wu, Tsung-Han, Yu, Ming-Chin, Hsieh, Sen-Yung
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container_issue 11
container_start_page 2946
container_title Cancers
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creator Lee, Chern-Horng
Hsu, Chiu-Yi
Yen, Tzung-Hai
Wu, Tsung-Han
Yu, Ming-Chin
Hsieh, Sen-Yung
description Cirrhosis is the primary risk factor for hepatocellular carcinoma (HCC) and gastrointestinal bleeding (GI). We aimed to assess the efficacy and safety of daily aspirin on HCC occurrence, overall survival, and GI bleeding in cirrhotic patients. A total of 35,898 eligible cases were enrolled for analyses from an initial 40,603 cirrhotic patients without tumor history. Patients continuously treated with aspirin for at least 84 days were in the therapy group, whereas those without treatment were controls. A 1:2 propensity score matching by age, sex, comorbidities, drugs, and significant clinical laboratory tests with covariate assessment was used. Multivariable regression analyses revealed that daily aspirin use was independently associated with a reduced risk of HCC (three-year HR 0.57; 95% CI 0.37-0.87; = 0.0091; five-year HR 0.63, 95% CI 0.45-0.88; = 0.0072) inversely correlated with the treatment duration [3-12 months: HR 0.88 (95% CI 0.58-1.34); 12-36 months: HR 0.56 (0.31-0.99); and ≥ 36 months: HR 0.37 (0.18-0.76)]. Overall mortality rates were significantly lower among aspirin users compared with untreated controls [three-year HR 0.43 (0.33-0.57); five-year HR 0.51 (0.42-0.63)]. Consistent results were obtained when the laboratory data were included in the propensity score for matching. Long-term aspirin use significantly reduced the incidence of HCC and overall mortality without increasing gastrointestinal bleeding in cirrhotic patients.
doi_str_mv 10.3390/cancers15112946
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We aimed to assess the efficacy and safety of daily aspirin on HCC occurrence, overall survival, and GI bleeding in cirrhotic patients. A total of 35,898 eligible cases were enrolled for analyses from an initial 40,603 cirrhotic patients without tumor history. Patients continuously treated with aspirin for at least 84 days were in the therapy group, whereas those without treatment were controls. A 1:2 propensity score matching by age, sex, comorbidities, drugs, and significant clinical laboratory tests with covariate assessment was used. Multivariable regression analyses revealed that daily aspirin use was independently associated with a reduced risk of HCC (three-year HR 0.57; 95% CI 0.37-0.87; = 0.0091; five-year HR 0.63, 95% CI 0.45-0.88; = 0.0072) inversely correlated with the treatment duration [3-12 months: HR 0.88 (95% CI 0.58-1.34); 12-36 months: HR 0.56 (0.31-0.99); and ≥ 36 months: HR 0.37 (0.18-0.76)]. Overall mortality rates were significantly lower among aspirin users compared with untreated controls [three-year HR 0.43 (0.33-0.57); five-year HR 0.51 (0.42-0.63)]. Consistent results were obtained when the laboratory data were included in the propensity score for matching. Long-term aspirin use significantly reduced the incidence of HCC and overall mortality without increasing gastrointestinal bleeding in cirrhotic patients.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15112946</identifier><identifier>PMID: 37296908</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antiplatelet therapy ; Aspirin ; Bleeding ; Cancer therapies ; Cirrhosis ; Comorbidity ; Diabetes ; Hepatitis B ; Hepatitis C ; Hepatocellular carcinoma ; Hepatoma ; Hospitalization ; Hypertension ; Laboratories ; Liver cancer ; Liver cirrhosis ; Liver diseases ; Medical research ; Medicine, Experimental ; Metastasis ; Mortality ; Patient outcomes ; Patients ; Risk factors ; Tumors</subject><ispartof>Cancers, 2023-05, Vol.15 (11), p.2946</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. 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We aimed to assess the efficacy and safety of daily aspirin on HCC occurrence, overall survival, and GI bleeding in cirrhotic patients. A total of 35,898 eligible cases were enrolled for analyses from an initial 40,603 cirrhotic patients without tumor history. Patients continuously treated with aspirin for at least 84 days were in the therapy group, whereas those without treatment were controls. A 1:2 propensity score matching by age, sex, comorbidities, drugs, and significant clinical laboratory tests with covariate assessment was used. Multivariable regression analyses revealed that daily aspirin use was independently associated with a reduced risk of HCC (three-year HR 0.57; 95% CI 0.37-0.87; = 0.0091; five-year HR 0.63, 95% CI 0.45-0.88; = 0.0072) inversely correlated with the treatment duration [3-12 months: HR 0.88 (95% CI 0.58-1.34); 12-36 months: HR 0.56 (0.31-0.99); and ≥ 36 months: HR 0.37 (0.18-0.76)]. 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We aimed to assess the efficacy and safety of daily aspirin on HCC occurrence, overall survival, and GI bleeding in cirrhotic patients. A total of 35,898 eligible cases were enrolled for analyses from an initial 40,603 cirrhotic patients without tumor history. Patients continuously treated with aspirin for at least 84 days were in the therapy group, whereas those without treatment were controls. A 1:2 propensity score matching by age, sex, comorbidities, drugs, and significant clinical laboratory tests with covariate assessment was used. Multivariable regression analyses revealed that daily aspirin use was independently associated with a reduced risk of HCC (three-year HR 0.57; 95% CI 0.37-0.87; = 0.0091; five-year HR 0.63, 95% CI 0.45-0.88; = 0.0072) inversely correlated with the treatment duration [3-12 months: HR 0.88 (95% CI 0.58-1.34); 12-36 months: HR 0.56 (0.31-0.99); and ≥ 36 months: HR 0.37 (0.18-0.76)]. Overall mortality rates were significantly lower among aspirin users compared with untreated controls [three-year HR 0.43 (0.33-0.57); five-year HR 0.51 (0.42-0.63)]. Consistent results were obtained when the laboratory data were included in the propensity score for matching. Long-term aspirin use significantly reduced the incidence of HCC and overall mortality without increasing gastrointestinal bleeding in cirrhotic patients.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37296908</pmid><doi>10.3390/cancers15112946</doi><orcidid>https://orcid.org/0000-0002-2756-678X</orcidid><orcidid>https://orcid.org/0000-0002-0907-1505</orcidid><orcidid>https://orcid.org/0000-0002-5083-8851</orcidid><orcidid>https://orcid.org/0000-0001-7171-3532</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antiplatelet therapy
Aspirin
Bleeding
Cancer therapies
Cirrhosis
Comorbidity
Diabetes
Hepatitis B
Hepatitis C
Hepatocellular carcinoma
Hepatoma
Hospitalization
Hypertension
Laboratories
Liver cancer
Liver cirrhosis
Liver diseases
Medical research
Medicine, Experimental
Metastasis
Mortality
Patient outcomes
Patients
Risk factors
Tumors
title Daily Aspirin Reduced the Incidence of Hepatocellular Carcinoma and Overall Mortality in Patients with Cirrhosis
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