Evidence map›Paper›PMID 37580675›Full record

ArticleBMC cancer2023

Defining aggressive prostate cancer: a geospatial perspective.

Daniel Wiese, Tesla D DuBois, Kristen A Sorice, Carolyn Y Fang, Camille Ragin, Mary B Daly, Adam C Reese, Kevin A Henry, Shannon M Lynch

Abstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Daniel WieseDepartment of Surveillance and Health Equity Science, American Cancer Society, 3380 Chastain Meadows Pkwy NW Suite 200, Kennesaw, GA, 30144, USA. daniel.wiese@cancer.org.
Tesla D DuBoisCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.
Kristen A SoriceCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.
Carolyn Y FangCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.
Camille RaginCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.
Mary B DalyCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.
Adam C ReeseTemple Health Urology, Philadelphia, PA, USA.
Kevin A HenryDepartment of Geography, Temple University, Philadelphia, PA, USA.
Shannon M LynchCancer Prevention and Control, Fox Chase Cancer Center, Philadelphia, PA, USA.

Funding

TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221704 · NCI · HUNTER COLLEGE · PI Ming-Chin Yeh · 2018 to 2026
$10.6M
NCI NIH HHS U54 CA221704NIH HHS U54 CA221704(5)
6 · The paper itself

Abstract

backgroundSpatial analysis can identify communities where men are at risk for aggressive prostate cancer (PCan) and need intervention. However, there are several definitions for aggressive PCan. In this study, we evaluate geospatial patterns of 3 different aggressive PCan definitions in relation to PCan-specific mortality and provide methodologic and practical insights into how each definition may affect intervention targets.

methodsUsing the Pennsylvania State Cancer Registry data (2005-2015), we used 3 definitions to assign "aggressive" status to patients diagnosed with PCan. Definition one (D1, recently recommended as the primary definition, given high correlation with PCan death) was based on staging criteria T4/N1/M1 or Gleason score ≥ 8. Definition two (D2, most frequently-used definition in geospatial studies) included distant SEER summary stage. Definition three (D3) included Gleason score ≥ 7 only. Using Bayesian spatial models, we identified geographic clusters of elevated odds ratios for aggressive PCan (binomial model) for each definition and compared overlap between those clusters to clusters of elevated hazard ratios for PCan-specific mortality (Cox regression).

resultsThe number of "aggressive" PCan cases varied by definition, and influenced quantity, location, and extent/size of geographic clusters in binomial models. While spatial patterns overlapped across all three definitions, using D2 in binomial models provided results most akin to PCan-specific mortality clusters as identified through Cox regression. This approach resulted in fewer clusters for targeted intervention and less sensitive to missing data compared to definitions that rely on clinical TNM staging.

conclusionsUsing D2, based on distant SEER summary stage, in future research may facilitate consistency and allow for standardized comparison across geospatial studies.

Indexed as

Prostatic NeoplasmsBayes TheoremHumansMaleNeoplasm StagingProstateProstate-Specific AntigenProstate-Specific AntigenAggressive prostate cancerGeospatialProstate cancerSurvival analysis

Identifiers

PMID37580675
PMCPMC10424402

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.