Evidence map›Paper›PMID 32581112›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2020

A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data.

Minh-Phuong Huynh-Le, Chun Chieh Fan, Roshan Karunamuni, Eleanor I Walsh, Emma L Turner, J Athene Lane, Richard M Martin, David E Neal, Jenny L Donovan, Freddie C Hamdy and 54 more

Abstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  4. Article
  5. Review
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  7. Article
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  9. Article
  10. Genetic Stratification of Age-Dependent Parkinson's Disease Risk by Polygenic Hazard Score.Movement disorders : official journal of the Movement Disorder Society · 2022
    Article
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  18. Review
  19. Prostate cancer.Nature reviews. Disease primers · 2021
    Review
  20. 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

64 authors.

Minh-Phuong Huynh-LeDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, California.ORCID 0000-0002-5025-4709
Chun Chieh FanCenter for Multimodal Imaging and Genetics, University of California San Diego, La Jolla, California.
Roshan KarunamuniDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, California.
Eleanor I WalshBristol Medical School, Department of Population Health Sciences, University of Bristol, Bristol, United Kingdom.ORCID 0000-0001-7696-3661
Emma L TurnerBristol Medical School, Department of Population Health Sciences, University of Bristol, Bristol, United Kingdom.ORCID 0000-0003-2575-387X
J Athene LaneBristol Medical School, Department of Population Health Sciences, University of Bristol, Bristol, United Kingdom.ORCID 0000-0003-4581-9346
Richard M MartinBristol Medical School, Department of Population Health Sciences, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-7992-7719
David E NealNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-6033-5086
Jenny L DonovanSchool of Social and Community Medicine, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-6488-5472
Freddie C HamdyNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
J Kellogg ParsonsDepartment of Urology, University of California, San Diego, La Jolla, California.
Rosalind A EelesThe Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-3698-6241
Douglas F EastonCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, United Kingdom.
Zsofia Kote-JaraiThe Institute of Cancer Research, London, United Kingdom.
Ali Amin Al OlamaCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, United Kingdom.ORCID 0000-0002-7178-3431
Sara Benlloch GarciaCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, United Kingdom.
Kenneth MuirDivision of Population Health, Health Services Research and Primary Care, University of Manchester, Oxford Road, Manchester, United Kingdom.ORCID 0000-0001-6429-988X
Henrik GrönbergDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0002-1073-2753
Fredrik WiklundDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0002-4623-0544
Markus AlyDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Johanna SchleutkerInstitute of Biomedicine, University of Turku, Turku, Finland.ORCID 0000-0002-1863-0305
Csilla SipekyInstitute of Biomedicine, University of Turku, Turku, Finland.
Teuvo Lj TammelaFaculty of Medicine and Health Technology, Prostate Cancer Research Center, Tampere University, Tampere, Finland.
Børge Grønne NordestgaardFaculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Timothy J KeyUniversity of Oxford, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-2294-307X
Ruth C TravisUniversity of Oxford, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9571-0763
Paul D P PharoahCentre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Strangeways Laboratory, Cambridge, United Kingdom.ORCID 0000-0001-8494-732X
Nora PashayanCentre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Strangeways Laboratory, Cambridge, United Kingdom.ORCID 0000-0003-0843-2468
Kay-Tee KhawClinical Gerontology Unit, University of Cambridge, Cambridge, United Kingdom.
Stephen N ThibodeauDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Shannon K McDonnellDivision of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, Minnesota.
Daniel J SchaidDivision of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, Minnesota.
Christiane MaierHumangenetik Tuebingen, Tuebingen, Germany.
Walther VogelInstitute for Human Genetics, University Hospital Ulm, Ulm, Germany.
Manuel LuedekeHumangenetik Tuebingen, Tuebingen, Germany.
Kathleen HerkommerTechnical University of Munich, School of Medicine, Klinikum rechts der Isar, Department of Urology, Munich, Germany.ORCID 0000-0002-0339-3394
Adam S KibelDivision of Urologic Surgery, Brigham and Womens Hospital, Boston, Massachusetts.
Cezary CybulskiInternational Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Dominika WokolorczykInternational Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Wojciech KluzniakInternational Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Lisa A Cannon-AlbrightDivision of Genetic Epidemiology, Department of Medicine, University of Utah School of Medicine, Salt Lake City, Utah.ORCID 0000-0003-2602-3668
Hermann BrennerDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0001-7494-9655
Ben SchöttkerDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-1217-4521
Bernd HolleczekDivision of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Jong Y ParkDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-6384-6447
Thomas A SellersDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, Florida.
Hui-Yi LinSchool of Public Health, Louisiana State University Health Sciences Center, New Orleans, Louisiana.ORCID 0000-0002-3307-5549
Chavdar Kroumov SlavovDepartment of Urology and Alexandrovska University Hospital, Medical University of Sofia, Sofia, Bulgaria.
Radka P KanevaMolecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical University of Sofia, Sofia, Bulgaria.
Vanio I MitevMolecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical University of Sofia, Sofia, Bulgaria.
Jyotsna BatraInstitute of Health and Biomedical Innovation and School of Biomedical Sciences, Queensland University of Technology, Brisbane, Queensland, Australia.
Judith A ClementsAustralian Prostate Cancer Research @Centre-Qld, Translational Research Institute, Brisbane, Queensland, Australia.
Manuel R TeixeiraDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.ORCID 0000-0002-4896-5982
Paula PauloDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Sofia MaiaDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Hardev PandhaThe University of Surrey, Guildford, Surrey, United Kingdom.
Agnieszka MichaelThe University of Surrey, Guildford, Surrey, United Kingdom.ORCID 0000-0002-7262-6227
Ian G MillsNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-5347-5083
Ole A AndreassenNORMENT, KG Jebsen Centre, Oslo University Hospital and University of Oslo, Oslo, Norway.
Anders M DaleCenter for Multimodal Imaging and Genetics, University of California San Diego, La Jolla, California.
Australian Prostate Cancer BioResource (APCB)
PRACTICAL Consortium

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
Translational Genomics Core (TGC)P20GM121288 · NIGMS · LSU HEALTH SCIENCES CENTER · PI Arunava Roy · 2017 to 2026
$22.4M
Improving assessment of prostate cancer bone metastases using advanced diffusion imagingK08EB026503 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEIBERT, TYLER MICHAEL · 2019 to 2022
$805k
Gene-Gene Interactions and Their Functional Roles in Prostate Cancer AggressivenessR21CA202417 · NCI · LSU HEALTH SCIENCES CENTER · PI LIN, HUI-YI · 2016 to 2017
$284k
Cancer Research UK 10118Cancer Research UK 15064Cancer Research UK 16563Cancer Research UK 19170Cancer Research UK 24432Cancer Research UK 29017Cancer Research UK 29019NCI NIH HHS L30 CA231417NCI NIH HHS P30 CA023100NCI NIH HHS R21 CA202417NIBIB NIH HHS K08 EB026503NIGMS NIH HHS P20 GM121288
6 · The paper itself

Abstract

backgroundA polygenic hazard score (PHS), the weighted sum of 54 SNP genotypes, was previously validated for association with clinically significant prostate cancer and for improved prostate cancer screening accuracy. Here, we assess the potential impact of PHS-informed screening.

methodsUnited Kingdom population incidence data (Cancer Research United Kingdom) and data from the Cluster Randomized Trial of PSA Testing for Prostate Cancer were combined to estimate age-specific clinically significant prostate cancer incidence (Gleason score ≥7, stage T3-T4, PSA ≥10, or nodal/distant metastases). Using HRs estimated from the ProtecT prostate cancer trial, age-specific incidence rates were calculated for various PHS risk percentiles. Risk-equivalent age, when someone with a given PHS percentile has prostate cancer risk equivalent to an average 50-year-old man (50-year-standard risk), was derived from PHS and incidence data. Positive predictive value (PPV) of PSA testing for clinically significant prostate cancer was calculated using PHS-adjusted age groups.

resultsThe expected age at diagnosis of clinically significant prostate cancer differs by 19 years between the 1st and 99th PHS percentiles: men with PHS in the 1st and 99th percentiles reach the 50-year-standard risk level at ages 60 and 41, respectively. PPV of PSA was higher for men with higher PHS-adjusted age.

conclusionsPHS provides individualized estimates of risk-equivalent age for clinically significant prostate cancer. Screening initiation could be adjusted by a man's PHS. IMPACT: Personalized genetic risk assessments could inform prostate cancer screening decisions.

Indexed as

AgedEarly Detection of CancerHumansMaleMiddle AgedNeoplasm GradingPopulation ControlProstatic Neoplasms

Identifiers

PMID32581112
PMCPMC7483627

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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.