Evidence map›Paper›PMID 33835822›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Impact of a Genomic Test on Treatment Decision in a Predominantly African American Population With Favorable-Risk Prostate Cancer: A Randomized Trial.

Adam B Murphy, Michael R Abern, Li Liu, Heidy Wang, Courtney M P Hollowell, Roohollah Sharifi, Patricia Vidal, Andre Kajdacsy-Balla, Marin Sekosan, Karen Ferrer and 6 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
4.1field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Adam B MurphyDepartment of Urology, Northwestern University, Chicago, IL.
Michael R AbernDepartment of Urology, University of Illinois at Chicago, Chicago, IL.
Li LiuDivision of Epidemiology and Biostatistics, University of Illinois at Chicago, Chicago, IL.
Heidy WangDivision of Epidemiology and Biostatistics, University of Illinois at Chicago, Chicago, IL.
Courtney M P HollowellDivision of Urology, Cook County Health and Hospital System, Chicago, IL.
Roohollah SharifiDepartment of Urology, Jesse Brown VA Medical Center, Chicago, IL.
Patricia VidalDivision of Urology, Cook County Health and Hospital System, Chicago, IL.
Andre Kajdacsy-BallaDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Marin SekosanDepartment of Pathology, Cook County Health and Hospital System, Chicago, IL.
Karen FerrerDepartment of Pathology, Cook County Health and Hospital System, Chicago, IL.
Shoujin WuPathology and Laboratory Services, Jesse Brown VA Medical Center, Chicago, IL.
Marlene GallegosPathology and Laboratory Services, Jesse Brown VA Medical Center, Chicago, IL.
Patrice King-LeeDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.
Lisa K SharpInstitute for Health Research and Policy, University of Illinois at Chicago, Chicago, IL.ORCID 0000-0002-7809-9042
Carol E FerransDepartment of Biobehavioral Nursing Science, University of Illinois at Chicago, Chicago, IL.
Peter H GannDepartment of Pathology, University of Illinois at Chicago, Chicago, IL.ORCID 0000-0002-9439-2900
University of Illinois Chicago · USCook County Health and Hospitals System · USJesse Brown VA Medical Center · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe Genomic Prostate Score (GPS), performed on biopsy tissue, predicts adverse outcome in prostate cancer (PCa) and has shown promise for improving patient selection for active surveillance (AS). However, its impact on treatment choice in high-risk populations of African Americans is largely unknown and, in general, the effect of the GPS on this difficult decision has not been evaluated in randomized trials.

methodsTwo hundred men with National Comprehensive Cancer Network very low to low-intermediate PCa from three Chicago hospitals (70% Black, 16% college graduates) were randomly assigned at diagnosis to standard counseling with or without a 12-gene GPS assay. The primary end point was treatment choice at a second postdiagnosis visit. The proportion of patients choosing AS was compared, and multivariable modeling was used to estimate the effects of various factors on AS acceptance.

resultsAS acceptance was high overall, although marginally lower in the intervention group (77%

conclusionIn contrast to other studies, the net effect of the GPS was to move patients away from AS, primarily among men with low health literacy. These findings have implications for our understanding of how prognostic molecular assays that generate probabilities of poor outcome can affect treatment decisions in diverse clinical populations.

Indexed as

AgedBlack or African AmericanGenomicsHumansMaleRisk Factors

Identifiers

PMID33835822
PMCPMC8148420
OpenAlexW3150341304

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.