Family History of Prostate and Breast Cancer Integrated with a Polygenic Risk Score Identifies Men at Highest Risk of Dying from Prostate Cancer before Age 75 Years

Author:

Plym Anna123ORCID,Zhang Yiwen2ORCID,Stopsack Konrad H.24ORCID,Jee Yon Ho2ORCID,Wiklund Fredrik3ORCID,Kibel Adam S.1ORCID,Kraft Peter25ORCID,Giovannucci Edward26ORCID,Penney Kathryn L.27ORCID,Mucci Lorelei A.2ORCID

Affiliation:

1. 1Urology Division, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

2. 2Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

3. 3Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

4. 4Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

5. 5Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

6. 6Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

7. 7Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.

Abstract

Abstract Purpose: Family history of prostate cancer is one of the few universally accepted risk factors for prostate cancer. How much an assessment of inherited polygenic risk for prostate cancer adds to lifetime risk stratification beyond family history is unknown. Experimental Design: We followed 10,120 men in the Health Professionals Follow-up Study with existing genotype data for risk of prostate cancer and prostate cancer–specific death. We assessed to what extent family history of prostate or breast cancer, combined with a validated polygenic risk score (PRS) including 269 prostate cancer risk variants, identifies men at risk of prostate cancer and prostate cancer death across the age span. Results: During 20 years of follow-up, 1,915 prostate cancer and 166 fatal prostate cancer events were observed. Men in the top PRS quartile with a family history of prostate or breast cancer had the highest rate of both prostate cancer and prostate cancer–specific death. Compared with men at lowest genetic risk (bottom PRS quartile and no family history), the HR was 6.95 [95% confidence interval (CI), 5.57–8.66] for prostate cancer and 4.84 (95% CI, 2.59–9.03) for prostate cancer death. Men in the two upper PRS quartiles (50%–100%) or with a family history of prostate or breast cancer (61.8% of the population) accounted for 97.5% of prostate cancer deaths by age 75 years. Conclusions: Our study shows that prostate cancer risk stratification on the basis of family history and inherited polygenic risk can identify men at highest risk of dying from prostate cancer before age 75 years.

Funder

National Cancer Institute

Prostate Cancer Foundation

Svenska Sällskapet för Medicinsk Forskning

Cancerfonden

DiNovi Family Foundation

William Casey

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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