Evidence map›Paper›PMID 31568648›Full record

ArticleCancer medicine2019

Self-Identified African Americans and prostate cancer risk: West African genetic ancestry is associated with prostate cancer diagnosis and with higher Gleason sum on biopsy.

William E Grizzle, Rick A Kittles, Soroush Rais-Bahrami, Ebony Shah, George W Adams, Mark S DeGuenther, Peter N Kolettis, Jeffrey W Nix, James E Bryant, Ravi Chinsky and 5 more

Abstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

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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

15 authors.

William E GrizzleDepartment of Pathology and Surgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Rick A KittlesDepartment of Population Sciences, City of Hope, Duarte, CA, USA.
Soroush Rais-BahramiDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL, USA.
Ebony ShahDepartment of Population Sciences, City of Hope, Duarte, CA, USA.
George W AdamsUrology Centers of Alabama, Homewood, AL, USA.
Mark S DeGuentherUrology Centers of Alabama, Homewood, AL, USA.
Peter N KolettisDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL, USA.
Jeffrey W NixDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL, USA.
James E BryantDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL, USA.
Ravi ChinskyTufts Medical Center, Boston, MA, USA.
James E KearnsTufts Medical Center, Boston, MA, USA.
Kerry DehimerTufts Medical Center, Boston, MA, USA.
Norma TerrinDepartment of Radiation Oncology, University of Miami Miller School of Medicine, Miami, FL, USA.
Hong ChangDepartment of Radiation Oncology, University of Miami Miller School of Medicine, Miami, FL, USA.
Sandra M GastonTufts Medical Center, Boston, MA, USA.ORCID 0000-0002-0564-0459

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Collaborative Human Tissue NetworkUM1CA183728 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GRIZZLE, WILLIAM E. · 2014 to 2018
$3.7M
Department of Defense Prostate Cancer Research Program W81XWH-10-1-0544Department of Defense Prostate Cancer Research Program W8XWH-10-1-0543NCI NIH HHS P30 CA013148NCI NIH HHS UM1 CA183728
6 · The paper itself

Abstract

Concerns about overtreatment of clinically indolent prostate cancer (PrCa) have led to recommendations that men who are diagnosed with low-risk PrCa be managed by active surveillance (AS) rather than immediate definitive treatment. However the risk of underestimating the aggressiveness of a patient's PrCa can be a significant source of anxiety and a barrier to patient acceptance of AS. The uncertainty is particularly keen for African American (AA) men who are about 1.7 times more likely to be diagnosed with PrCa than European American (EA) men and about 2.4 times more likely to die of this disease. The AA population, as many other populations in the Americas, is genetically heterogeneous with varying degrees of admixture from West Africans (WAs), Europeans, and Native Americans (NAs). Recommendations for PrCa screening and management rarely consider potential differences in risk within the AA population. We compared WA genetic ancestry in AA men undergoing standard prostate biopsy who were diagnosed with no cancer, low-grade PrCa (Gleason Sum 6), or higher grade PrCa (Gleason Sum 7-10). We found that WA genetic ancestry was significantly higher in men who were diagnosed with PrCa on biopsy, compared to men who were cancer-negative, and highest in men who were diagnosed with higher grade PrCa (Gleason Sum 7-10). Incorporating WA ancestry into the guidelines for making decisions about when to obtain a biopsy and whether to choose AS may allow AA men to personalize their approach to PrCa screening and management.

Indexed as

Africa, WesternAgedBiopsyBlack or African AmericanBlack PeopleHumansMaleMiddle AgedNeoplasm GradingProstatic NeoplasmsRiskAfrican Americanprostate biopsyprostate cancerWest African ancestry

Identifiers

PMID31568648
PMCPMC6853835

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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.