Evidence map›Paper›PMID 40121103›Full record

ArticleUrologic oncology2025

Does inclusion of neighborhood variables improve clinical risk prediction for advanced prostate cancer in Black and White men?

Erin K Tagai, Elizabeth A Handorf, Kristen A Sorice, Carolyn Y Fang, Mengying Deng, Mary B Daly, Adam C Reese, Kevin A Henry, Camille Ragin, Shannon M Lynch

Abstract read
In one paragraph

Article in Urologic oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Erin K TagaiCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA. Electronic address: erin.tagai@fccc.edu.
Elizabeth A HandorfPopulation Studies Facility, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Kristen A SoriceCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Carolyn Y FangCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Mengying DengPopulation Studies Facility, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Mary B DalyCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Adam C ReeseDepartment of Urology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA.
Kevin A HenryDepartment of Geography, Temple University, Philadelphia, PA.
Camille RaginCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.
Shannon M LynchCancer Prevention and Control, Fox Chase Cancer Center/Temple University Health System, Philadelphia, PA.

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Eric Andrew Ross · 1985 to 2026
$138.8M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221705 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI GRACE X. MA · 2018 to 2026
$16.3M
NCI NIH HHS P30 CA006927NCI NIH HHS U54 CA221705
6 · The paper itself

Abstract

introductionBlack men are diagnosed with high-grade prostate cancer (PCa; Gleason sum ≥7) at greater rates than White men. This persistent disparity has led to mortality rates among Black men that are twice the rate of White men. Risk prediction tools can aid clinical decision making for PCa screening, biopsy, and treatment. However, research has not integrated neighborhood-level risk factors that are associated with rates of high-grade PCa. This study sought to determine whether inclusion of neighborhood-level variables can improve prediction of high-grade PCa over the existing Prostate Cancer Prevention Trial (PCPT) calculator.

methodsExisting PCa cases from 2005 to 2017 were ascertained from urology, radiation, and medical oncology clinics at Fox Chase Cancer Center/Temple University Health System (FCCC/TUHS). Existing databases from patient medical records, biosamples, pathology, and neighborhood data from the U.S. census were linked via geocodes. Informed by prior studies that selected social environmental variables, a series of logistic regression models were completed to predict the probability of high-grade PCa on prespecified sets of variables from the PCPT.

resultsOur best fitting, multilevel model included PCPT variables (i.e., PSA, digital rectal exam, age, race, prior biopsy, family history) as well as insurance status, neighborhood-level poverty, residence in a high risk PCa cluster, and % of Employed Men in Protective Service Occupations. However, the AUC for this model (0.673) was only marginally improved from the initial model of only PCPT variables (0.671). Further, in separate analyses by race (White, Black) the % of Employed Men in Protective Service Occupations was only significant among White men. DISCUSSION: Study findings demonstrate the potential for neighborhood variables to enhance current risk prediction models and identify interaction effects revealing differences across subgroups, such as race. The lack of significant associations between neighborhood variables and Black men highlight the complexity of systemic racism and neighborhood-level variables on PCa outcomes.

Indexed as

Black or African AmericanNeighborhood CharacteristicsProstatic NeoplasmsWhiteAgedHumansMaleMiddle AgedRisk AssessmentRisk FactorsHealth inequitiesProstate cancerRisk assessmentSociodemographic

Identifiers

PMID40121103
PMCPMC12068980

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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.