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Cancer Epidemiology, Biomarkers & Prevention
Cancer Epidemiology, Biomarkers & Prevention
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Null Results in Brief

A Prospective Study of Aspirin Use and Prostate Cancer Risk by TMPRSS2:ERG Status

Konrad H. Stopsack, Amparo G. Gonzalez-Feliciano, Samuel F. Peisch, Mary K. Downer, Riley A. Gage, Stephen Finn, Rosina T. Lis, Rebecca E. Graff, Andreas Pettersson, Claire H. Pernar, Massimo Loda, Philip W. Kantoff, Thomas U. Ahearn and Lorelei A. Mucci; on behalf of the Transdisciplinary Prostate Cancer Partnership (ToPCaP)
Konrad H. Stopsack
1Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
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  • ORCID record for Konrad H. Stopsack
  • For correspondence: stopsack@mskcc.org
Amparo G. Gonzalez-Feliciano
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
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Samuel F. Peisch
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
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Mary K. Downer
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
3Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
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Riley A. Gage
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
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Stephen Finn
4Department of Pathology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
5Department of Pathology, Trinity College Dublin, Dublin, Ireland.
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Rosina T. Lis
6Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
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Rebecca E. Graff
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
7Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California.
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Andreas Pettersson
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
8Department of Medicine, Clinical Epidemiology Unit, Solna, Karolinska Institutet, Stockholm, Sweden.
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Claire H. Pernar
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
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Massimo Loda
4Department of Pathology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
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Philip W. Kantoff
1Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
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Thomas U. Ahearn
9National Cancer Institute, Division of Cancer Epidemiology and Genetics, Epidemiology and Biostatistics Program, Bethesda, Maryland.
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Lorelei A. Mucci
2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
3Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
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DOI: 10.1158/1055-9965.EPI-18-0510
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Abstract

Background: In a case–control study, aspirin use was associated with a lower risk of a common prostate cancer molecular subtype, the TMPRSS2:ERG gene fusion. We sought to validate this finding in a prospective cohort.

Methods: 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. TMPRSS2:ERG 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.

Results: In multivariable models, we found no association between regular use of aspirin and risk of ERG-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.

Conclusions: 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 ERG-positive prostate cancer.

Impact: 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 TMPRSS2:ERG fusion. Cancer Epidemiol Biomarkers Prev; 1–3. ©2018 AACR.

  • Received May 10, 2018.
  • Revision received May 30, 2018.
  • Accepted July 30, 2018.
  • Published first August 14, 2018.
  • ©2018 American Association for Cancer Research.
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A Prospective Study of Aspirin Use and Prostate Cancer Risk by TMPRSS2:ERG Status
Konrad H. Stopsack, Amparo G. Gonzalez-Feliciano, Samuel F. Peisch, Mary K. Downer, Riley A. Gage, Stephen Finn, Rosina T. Lis, Rebecca E. Graff, Andreas Pettersson, Claire H. Pernar, Massimo Loda, Philip W. Kantoff, Thomas U. Ahearn and Lorelei A. Mucci on behalf of the Transdisciplinary Prostate Cancer Partnership (ToPCaP)
Cancer Epidemiol Biomarkers Prev September 10 2018 DOI: 10.1158/1055-9965.EPI-18-0510

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A Prospective Study of Aspirin Use and Prostate Cancer Risk by TMPRSS2:ERG Status
Konrad H. Stopsack, Amparo G. Gonzalez-Feliciano, Samuel F. Peisch, Mary K. Downer, Riley A. Gage, Stephen Finn, Rosina T. Lis, Rebecca E. Graff, Andreas Pettersson, Claire H. Pernar, Massimo Loda, Philip W. Kantoff, Thomas U. Ahearn and Lorelei A. Mucci on behalf of the Transdisciplinary Prostate Cancer Partnership (ToPCaP)
Cancer Epidemiol Biomarkers Prev September 10 2018 DOI: 10.1158/1055-9965.EPI-18-0510
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