Evidence map›Paper›PMID 33792945›Full record

ArticleThe Prostate2021

Comparison of germline mutations in African American and Caucasian men with metastatic prostate cancer.

Elisa M Ledet, Earle F Burgess, Alexandra O Sokolova, Ellen B Jaeger, Whitley Hatton, Marcus Moses, Patrick Miller, Patrick Cotogno, Jodi Layton, Pedro Barata and 13 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Prostate, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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  19. Prevalence of GermlineCancers · 2023
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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

23 authors at 8 institutions in 1 country.

Elisa M LedetDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.ORCID 0000-0003-1230-3255
Earle F BurgessGenitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
Alexandra O SokolovaDivision of Oncology, Department of Medicine, University of Washington Medical Center/Fred Hutchinson Cancer Research Center/VA Puget Sound HCS, Seattle, Washington, USA.
Ellen B JaegerDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Whitley HattonDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Marcus MosesSchool of Medicine, Tulane University, New Orleans, Louisiana, USA.
Patrick MillerDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Patrick CotognoDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Jodi LaytonDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Pedro BarataDeming Department of Medicine, Tulane University, New Orleans, Louisiana, USA.
Brian E LewisDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.
Mari NakazawaThe Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, Maryland, USA.
Jason ZhuGenitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
Beth DellingerGenitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
Sara ElrefaiGenitourinary Oncology Section, Levine Cancer Institute/Atrium Health, Charlotte, North Carolina, USA.
Nellie N NafissiInternal Medicine, Mayo Clinic, Phoenix, Arizona, USA.ORCID 0000-0003-0436-5931
Jan B EganCenter for Individualized Medicine, Mayo Clinic, Scottsdale, Arizona, USA.
Neal ShoreCarolina Urologic Research Center, Atlantic Urology Clinics, Myrtle Beach, South Carolina, USA.
Rana R McKayMoores Cancer Center, University of California San Diego, La Jolla, California, USA.
Alan H BryceDivision of Hematology/Oncology, Mayo Clinic Cancer Center, Mayo Clinic, Phoenix, Arizona, USA.ORCID 0000-0002-0206-3895
Heather H ChengDivision of Oncology, Department of Medicine, University of Washington Medical Center/Fred Hutchinson Cancer Research Center/VA Puget Sound HCS, Seattle, Washington, USA.ORCID 0000-0002-1365-0702
Emmanuel S AntonarakisThe Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0003-0031-9655
Oliver SartorDepartment of Medicine, Tulane Cancer Center, Tulane University, New Orleans, Louisiana, USA.ORCID 0000-0002-8777-7343
Tulane University · USLevine Cancer Institute · USJohns Hopkins University · USUniversity of Puget Sound · USWinnMed · USCarolina Urologic Research Center · USMayo Clinic · USUniversity of California San Diego · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

backgroundThe goal of this study is to evaluate germline genetic variants in African American men with metastatic prostate cancer as compared to those in Caucasian men with metastatic prostate cancer in an effort to understand the role of genetic factors in these populations.

methodsAfrican American and Caucasian men with metastatic prostate cancer who had germline testing using multigene panels were used to generate comparisons. Germline genetic results, clinical parameters, and family histories between the two populations were analyzed.

resultsA total of 867 patients were included in this retrospective study, including 188 African American and 669 Caucasian patients. There was no significant difference in the likelihood of a pathogenic or likely-pathogenic variants (PV/LPVs) between African American and Caucasian patients (p = .09). African American patients were more likely to have a variant of unknown significance than Caucasians (odds ratio [OR] = 1.95; p < .0001). BRCA1 PV/LPVs were higher in African Americans (OR = 4.86; p = .04). African American patients were less likely to have a PV/LPV in non-BRCA DNA repair genes (OR = 0.30; p = .008). Family history of breast (OR = 2.09; p = .002) or ovarian cancer (OR = 2.33; p = .04) predicted PV/LPVs in Caucasians but not African-Americans. This underscores the limitations of family history in AA men and the importance of personal history to guide germline testing in AA men.

conclusionsIn metastatic prostate cancer patients, PV/LPVs of tested genes did not vary by race, BRCA1 PV/LPVs were more common in the African American subset. However, PV/LPVs in non-BRCA DNA repair genes were less likely to be encountered in African Americans. Family history associated with genetic testing results in Caucasians only.

Indexed as

Germ-Line MutationBlack or African AmericanBRCA2 ProteinHumansMaleMiddle AgedNeoplasm MetastasisProstatic NeoplasmsWhite PeopleBRCA2 ProteinAfrican Americangeneticsgermlinemetastatic prostate cancerpathogenic variantsracial disparity

Identifiers

PMID33792945
PMCPMC8252583
OpenAlexW3149925202

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.