» Articles » PMID: 28213047

The Effect of Combined Aspirin and Clopidogrel Treatment on Cancer Incidence

Overview
Journal Am J Med
Specialty General Medicine
Date 2017 Feb 19
PMID 28213047
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Multiple studies have shown an association between aspirin treatment and a reduction in newly diagnosed cancer. Conversely, there are conflicting clinical and laboratory data on the effect of combined clopidogrel and aspirin therapy on cancer incidence, including analyses suggesting an increased cancer risk. No large-scale cohort study has been performed to address this issue in a heterogeneous real-world scenario. We investigated the effect of clopidogrel and aspirin on cancer incidence compared with aspirin alone and no antiplatelet therapy.

Methods: A population-based historical cohort study of subjects aged ≥50 years covered by Clalit Health Services, an Israeli health maintenance organization, was performed. Patients treated with the newer antiplatelet drugs, prasugrel or ticagrelor, which, like clopidogrel, inhibit adenosine diphosphate receptors, and those with prior cancer were excluded. Prescription records of antiplatelet medication were retrieved.

Results: The cohort included 183,912 subjects diagnosed with 21,974 cancer cases based upon the International Classification of Diseases, Ninth Revision. Dual aspirin and clopidogrel was prescribed in 9.6%, while 49% received aspirin alone and 41% used neither. Compared with nonusers, there was a lower risk of cancer in subjects exposed to aspirin with (hazard ratio [HR] 0.46; 95% confidence interval [CI], 0.44-0.49) or without clopidogrel (HR 0.54; 95% CI, 0.52-0.56), on long-term follow-up. Combined treatment was associated with a lower cancer risk than the aspirin-only group (HR 0.92; 95% CI, 0.86-0.97).

Conclusions: Dual clopidogrel and aspirin treatment is safe regarding the cancer risk. This study generates the hypothesis that clopidogrel may reduce cancer incidence.

Citing Articles

Role and recent progress of P2Y12 receptor in cancer development.

Xi Y, Min Z, Liu M, Lin X, Yuan Z Purinergic Signal. 2024; .

PMID: 38874752 DOI: 10.1007/s11302-024-10027-w.


Mechanisms of platelet activation in cancer-associated thrombosis: a focus on myeloproliferative neoplasms.

Bekendam R, Ravid K Front Cell Dev Biol. 2023; 11:1207395.

PMID: 37457287 PMC: 10342211. DOI: 10.3389/fcell.2023.1207395.


Aspirin and Primary Cancer Risk Reduction in Ischemic Cardiac or Cerebrovascular Disease Survivors: A Nationwide Population-Based Propensity-Matched Cohort Study.

Liao Y, Hsu R, Wang T, Wu C, Huang S, Hsu C Cancers (Basel). 2023; 15(1).

PMID: 36612095 PMC: 9817941. DOI: 10.3390/cancers15010097.


Targeting Platelet Activation Pathways to Limit Tumour Progression: Current State of Affairs.

Xulu K, Augustine T Pharmaceuticals (Basel). 2022; 15(12).

PMID: 36558983 PMC: 9784118. DOI: 10.3390/ph15121532.


Secretory SERPINE1 Expression Is Increased by Antiplatelet Therapy, Inducing MMP1 Expression and Increasing Colon Cancer Metastasis.

Kim W, Mun J, Baek S, Kim M, Yang G, Jeong M Int J Mol Sci. 2022; 23(17).

PMID: 36076991 PMC: 9455756. DOI: 10.3390/ijms23179596.