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Genetically adjusted PSA levels for prostate cancer screening

Kachuri, Linda (author)
University of California, San Francisco
Hoffmann, Thomas J (author)
University of California, San Francisco
Jiang, Yu (author)
Stanford University
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Berndt, Sonja I (author)
National Cancer Institute, USA
Shelley, John P (author)
Vanderbilt University Medical Center
Schaffer, Kerry R (author)
Vanderbilt-Ingram Cancer Center
Machiela, Mitchell J (author)
National Cancer Institute, USA
Freedman, Neal D (author)
National Cancer Institute, USA
Huang, Wen-Yi (author)
National Cancer Institute, USA
Li, Shengchao A (author)
National Cancer Institute, USA
Easterlin, Ryder (author)
Goodman, Phyllis J (author)
Till, Cathee (author)
Thompson, Ian (author)
Lilja, Hans (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Clinical Chemistry, Malmö,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Memorial Sloan-Kettering Cancer Center,Skåne University Hospital
Van Den Eeden, Stephen K (author)
Chanock, Stephen J (author)
Haiman, Christopher A (author)
Conti, David V (author)
Klein, Robert J (author)
Mosley, Jonathan D (author)
Graff, Rebecca E (author)
Witte, John S (author)
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 (creator_code:org_t)
2023
2023
English.
In: Nature Medicine. - 1546-170X. ; 29:6, s. 1412-1423
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Prostate-specific antigen (PSA) screening for prostate cancer remains controversial because it increases overdiagnosis and overtreatment of clinically insignificant tumors. Accounting for genetic determinants of constitutive, non-cancer-related PSA variation has potential to improve screening utility. In this study, we discovered 128 genome-wide significant associations (P < 5 × 10 -8) in a multi-ancestry meta-analysis of 95,768 men and developed a PSA polygenic score (PGS PSA) that explains 9.61% of constitutive PSA variation. We found that, in men of European ancestry, using PGS-adjusted PSA would avoid up to 31% of negative prostate biopsies but also result in 12% fewer biopsies in patients with prostate cancer, mostly with Gleason score <7 tumors. Genetically adjusted PSA was more predictive of aggressive prostate cancer (odds ratio (OR) = 3.44, P = 6.2 × 10 -14, area under the curve (AUC) = 0.755) than unadjusted PSA (OR = 3.31, P = 1.1 × 10 -12, AUC = 0.738) in 106 cases and 23,667 controls. Compared to a prostate cancer PGS alone (AUC = 0.712), including genetically adjusted PSA improved detection of aggressive disease (AUC = 0.786, P = 7.2 × 10 -4). Our findings highlight the potential utility of incorporating PGS for personalized biomarkers in prostate cancer screening.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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