TY - JOUR
T1 - Effect of aspirin on incidence, recurrence, and mortality in prostate cancer patients
T2 - integrating evidence from randomized controlled trials and real-world studies
AU - Ma, Shaodi
AU - Xia, Weihang
AU - Wu, Birong
AU - Sun, Chenyu
AU - Jiang, Yuemeng
AU - Liu, Haixia
AU - Lowe, Scott
AU - Zhou, Zhen
AU - Xie, Peng
AU - Gao, Juan
AU - Feng, Linya
AU - Guo, Xianwei
AU - Qu, Guangbo
AU - Sun, Yehuan
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2023/11
Y1 - 2023/11
N2 - Purpose: Aspirin has been suggested to reduce the risk of cancer. However, previous studies have been inconsistent regarding the relationship between aspirin use and the risk of occurrence of prostate cancer (PCa). The purpose of this study was to assess the effect of aspirin on clinical outcomes in patients with PCa in a meta-analysis and to explore the possible dose-response relationship. Methods: A systematic literature search was conducted in 10 electronic databases and 4 registries. The combined relative risks (RRs) were calculated using a random-effects model with 95% confidence interval (CIs) to assess the effect of aspirin on the risk of PCa. Relevant subgroup analyses and sensitivity analyses were performed. Results: The across studies results show that aspirin use associated with lower incidence of PCa (RR: 0.96, 95% CI: 0.95–0.98), and reduced mortality (RR: 0.88, 95% CI: 0.82–0.95). The results of the subgroup analysis indicated that both cohort and population studies in the Americas showed a reduction in PCa incidence and mortality with aspirin use. A linear correlation was observed between dosage/duration of aspirin use and its protective effect. Additionally, post-diagnosis aspirin use was associated with decreased risk of PCa mortality. Conclusions: This meta-analysis revealed an independent correlation between the use of aspirin and reductions in both the incidence and mortality rates of PCa. However, randomized controlled trials did not find any association between aspirin use and PCa. Furthermore, the impact of aspirin on PCa occurrence was found to be dependent on both dosage and duration.
AB - Purpose: Aspirin has been suggested to reduce the risk of cancer. However, previous studies have been inconsistent regarding the relationship between aspirin use and the risk of occurrence of prostate cancer (PCa). The purpose of this study was to assess the effect of aspirin on clinical outcomes in patients with PCa in a meta-analysis and to explore the possible dose-response relationship. Methods: A systematic literature search was conducted in 10 electronic databases and 4 registries. The combined relative risks (RRs) were calculated using a random-effects model with 95% confidence interval (CIs) to assess the effect of aspirin on the risk of PCa. Relevant subgroup analyses and sensitivity analyses were performed. Results: The across studies results show that aspirin use associated with lower incidence of PCa (RR: 0.96, 95% CI: 0.95–0.98), and reduced mortality (RR: 0.88, 95% CI: 0.82–0.95). The results of the subgroup analysis indicated that both cohort and population studies in the Americas showed a reduction in PCa incidence and mortality with aspirin use. A linear correlation was observed between dosage/duration of aspirin use and its protective effect. Additionally, post-diagnosis aspirin use was associated with decreased risk of PCa mortality. Conclusions: This meta-analysis revealed an independent correlation between the use of aspirin and reductions in both the incidence and mortality rates of PCa. However, randomized controlled trials did not find any association between aspirin use and PCa. Furthermore, the impact of aspirin on PCa occurrence was found to be dependent on both dosage and duration.
KW - Aspirin
KW - Dose-response relationship
KW - Meta-analysis
KW - Prostate cancer
UR - https://www.scopus.com/pages/publications/85169160737
U2 - 10.1007/s00228-023-03556-7
DO - 10.1007/s00228-023-03556-7
M3 - Article
C2 - 37648741
AN - SCOPUS:85169160737
SN - 0031-6970
VL - 79
SP - 1475
EP - 1503
JO - European Journal of Clinical Pharmacology
JF - European Journal of Clinical Pharmacology
ER -