Evidence map›Paper›PMID 27197965›Full record

ArticleThe Prostate2016

Adding genetic risk score to family history identifies twice as many high-risk men for prostate cancer: Results from the prostate cancer prevention trial.

Haitao Chen, Xu Liu, Charles B Brendler, Donna P Ankerst, Robin J Leach, Phyllis J Goodman, M Scott Lucia, Catherine M Tangen, Li Wang, Fang-Chi Hsu and 8 more

Open access · greenAbstract readControlled Clinical Trial
In one paragraph

Article in The Prostate, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Can polygenic risk scores contribute to cost-effective cancer screening? A systematic review.Genetics in medicine : official journal of the American College of Medical Genetics · 2022
    Pooled it
  2. Trial
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  6. CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
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  8. Review
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  16. Flype: Software for enabling personalized medicine.American journal of medical genetics. Part C, Seminars in medical genetics · 2021
    Article
  17. Article
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  19. Article
  20. A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 9 institutions in 3 countries.

Haitao ChenState Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, China.
Xu LiuState Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, China.
Charles B BrendlerDepartment of Surgery, NorthShore University HealthSystem, Evanston, Illinois.
Donna P AnkerstDepartment of Urology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Robin J LeachDepartment of Urology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Phyllis J GoodmanPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
M Scott LuciaUniversity of Colorado Denver School of Medicine, Aurora, Colorado.
Catherine M TangenPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Li WangCenter for Cancer Genomics, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Fang-Chi HsuCenter for Cancer Genomics, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Jielin SunCenter for Cancer Genomics, Wake Forest School of Medicine, Winston-Salem, North Carolina.
A Karim KaderDepartment of Urology, UC San Diego Health System, San Diego, California.
William B IsaacsDepartment of Urology and the James Buchanan Brady Urologic Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Brian T HelfandDepartment of Surgery, NorthShore University HealthSystem, Evanston, Illinois.
S Lilly ZhengCenter for Cancer Genomics, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Ian M ThompsonDepartment of Urology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Elizabeth A PlatzDepartment of Urology and the James Buchanan Brady Urologic Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jianfeng XuState Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, China.
Wake Forest University · USFudan University · CNFred Hutch Cancer Center · USJohns Hopkins University · USNorthShore University HealthSystem · USThe University of Texas Health Science Center at San Antonio · USTechnical University of Munich · DEUC San Diego Health System · USUniversity of Colorado Denver · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
SWOG Foreign AccrualsU10CA037429 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BLANKE, CHARLES D., MEYSKENS, FRANK L. · 1985 to 2014
$205.2M
University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
SWOG NCORP Research BaseUG1CA189974 · NCI · THE HOPE FOUNDATION · PI CHARLES D. BLANKE, DAWN HERSHMAN · 2014 to 2026
$80.6M
TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
SAN ANTONIO CENTER OF BIOMARKERS OF RISK FOR PROSTATE CAU01CA086402 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LEACH, ROBIN JEAN, THOMPSON, IAN M. · 2000 to 2018
$33.1M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Oxidative Damage and DNA Repair in the PCPTP01CA108964 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI THOMPSON, IAN M · 2005 to 2009
$13.6M
PCPT and SELECT cohorts: Core Infrastructure Support for Cancer Research UM1CA182883 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TANGEN, CATHERINE M., THOMPSON, IAN M. · 2013 to 2017
$5.2M
Clinical validity and utility of genomic targeted chemoprevention of PCaUC2CA148463 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI XU, JIANFENG · 2010 to 2010
$2.0M
Clinical validity and utility of genomic targeted chemoprevention of PCaRC2CA148463 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI XU, JIANFENG · 2009 to 2009
$2.0M
Genetic profiling in PCPT: prostate cancer risk, PSA levels, and chemopreventionR01CA140262 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PLATZ, ELIZABETH A., XU, JIANFENG · 2009 to 2011
$1.9M
NCI NIH HHS P01 CA108964NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA046934NCI NIH HHS P30 CA054174NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA140262NCI NIH HHS RC2 CA148463NCI NIH HHS U01 CA086402NCI NIH HHS U10 CA037429NCI NIH HHS UC2 CA148463NCI NIH HHS UG1 CA189974NCI NIH HHS UM1 CA182883
6 · The paper itself

Abstract

backgroundWhile family history (FH) has been widely used to provide risk information, it captures only a small proportion of subjects with higher genetic susceptibility. Our objective is to assess whether a genetic risk score (GRS) calculated from prostate cancer (PCa) risk-associated single nucleotide polymorphisms (SNPs) can supplement FH for more effective risk stratification for PCa screening decision-making.

methodsA GRS was calculated based on 29 PCa risk-associated SNPs for 4,528 men of European descent in the placebo arm of the Prostate Cancer Prevention Trial (PCPT). At study entry, participants were free of PCa diagnosis. Performance of FH and GRS were measured by observed detection rate of PCa and high-grade PCa (Gleason score ≥7) during the 7-year study.

resultsGRS was a significant predictor of PCa in men with or without a positive FH (P = 1.18 × 10(-4) and P = 4.50 × 10(-16) , respectively). Using FH alone, as expected, the 17% of men who were FH+ had a PCa detection rate that was significantly higher (29.02%) than FH- men (23.43%, P = 0.001). When both FH+ or GRS >1.4 are considered, more than twice as many men (36%) can be classified as higher risk, as evidenced by a significantly higher PCa detection rate (30.98%) than in the remaining men (20.61%, P = 5.30 × 10(-15) ). If targeting only FH+ men, four out of five PCa cases would go undetected, as would a similarly large fraction (∼80%) of high-grade PCa cases. In comparison, if targeting FH+ or GRS >1.4 men, almost half of all PCa cases would be detected, including 45% of high-grade PCa cases.

conclusionsA prostate cancer GRS can supplement family history to better identify higher risk men for targeted intervention. Prostate 76:1120-1129, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

Genetic Predisposition to DiseaseHumansMaleMedical History TakingMiddle AgedNeoplasm GradingPlacebosPolymorphism, Single NucleotideProstatic NeoplasmsRisk AssessmentRisk FactorsWhite PeoplePlacebosfamily historyprostate cancerrisksingle nucleotide polymorphismsthe prostate cancer prevention trial

Identifiers

PMID27197965
PMCPMC5501387
OpenAlexW2403217808

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.