Title | A Prospective Study of Aspirin Use and Prostate Cancer Risk by Status. |
Publication Type | Journal Article |
Year of Publication | 2018 |
Authors | Stopsack KH, Gonzalez-Feliciano AG, Peisch SF, Downer MK, Gage RA, Finn S, Lis RT, Graff RE, Pettersson A, Pernar CH, Loda M, Kantoff PW, Ahearn TU, Mucci LA |
Corporate Authors | Transdisciplinary Prostate Cancer Partnership(ToPCaP) |
Journal | Cancer Epidemiol Biomarkers Prev |
Volume | 27 |
Issue | 10 |
Pagination | 1231-1233 |
Date Published | 2018 10 |
ISSN | 1538-7755 |
Keywords | Adult, Aged, Anti-Inflammatory Agents, Non-Steroidal, Aspirin, Follow-Up Studies, Humans, Incidence, Male, Middle Aged, Oncogene Proteins, Fusion, Prognosis, Prospective Studies, Prostatic Neoplasms, United States |
Abstract | In a case-control study, aspirin use was associated with a lower risk of a common prostate cancer molecular subtype, the gene fusion. We sought to validate this finding in a prospective cohort. In the Health Professionals Follow-up Study, 49,395 men reported on aspirin use on biennial questionnaires and were followed for prostate cancer incidence over 23 years. status was assessed by IHC for presence of ERG on archival tumor specimens for 912 patients with prostate cancer, of whom 48% were ERG-positive. In multivariable models, we found no association between regular use of aspirin and risk of -positive prostate cancer (HR, 1.02; 95% confidence interval, 0.85-1.23), nor any association with duration or frequency of aspirin use. In restricting to cases with either high Gleason grade or advanced stage disease, there remained no association with aspirin use. Data from this prospective study with repeated assessments of aspirin use do not support the hypothesis that aspirin use is associated with a lower risk of -positive prostate cancer. Aspirin use is unlikely to lower the risk of this common molecular subtype of prostate cancer. However, there is emerging data supporting the role of other lifestyle and genetic factors underlying the development of the fusion. . |
DOI | 10.1158/1055-9965.EPI-18-0510 |
Alternate Journal | Cancer Epidemiol Biomarkers Prev |
PubMed ID | 30108097 |
PubMed Central ID | PMC6170677 |
Grant List | P50 CA090381 / CA / NCI NIH HHS / United States R25 CA112355 / CA / NCI NIH HHS / United States U01 CA167552 / CA / NCI NIH HHS / United States P30 CA008748 / CA / NCI NIH HHS / United States T32 CA009001 / CA / NCI NIH HHS / United States R01 CA136578 / CA / NCI NIH HHS / United States P30 CA006516 / CA / NCI NIH HHS / United States |
Related Faculty:
Massimo Loda, M.D.