Evidence map›Paper›PMID 40834325›Full record

ArticleJCO precision oncology2025

Sociodemographic Features, Health Care Costs, and Treatment Implications of Genomic Classifier Testing for Localized Prostate Cancer in the United States.

James R Janopaul-Naylor, Dattatraya Patil, Shreyas Joshi, Martin G Sanda, Nikhil Sebastian, Kamran Salari, Jade Dodge, Vishal R Dhere, Bruce W Hershatter, Pretesh R Patel and 3 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2025. 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. Review
  2. Review
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

13 authors.

James R Janopaul-NaylorDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-3612-4852
Dattatraya PatilDepartment of Urology, Emory University, Atlanta, GA.
Shreyas JoshiDepartment of Urology, Emory University, Atlanta, GA.
Martin G SandaDepartment of Urology, Emory University, Atlanta, GA.
Nikhil SebastianDepartment of Radiation Oncology, Emory University, Atlanta, GA.
Kamran SalariDepartment of Radiation Oncology, Emory University, Atlanta, GA.ORCID 0000-0002-3314-4196
Jade DodgeDrexel University School of Medicine, Philadelphia, PA.
Vishal R DhereDepartment of Radiation Oncology, Emory University, Atlanta, GA.ORCID 0000-0002-8364-7488
Bruce W HershatterDepartment of Radiation Oncology, Emory University, Atlanta, GA.
Pretesh R PatelDepartment of Radiation Oncology, Emory University, Atlanta, GA.
Ashesh B JaniDepartment of Radiation Oncology, Emory University, Atlanta, GA.ORCID 0000-0002-1687-6221
Christopher FilsonDepartment of Urology, Bernard J Tyson Kaiser Permanente School of Medicine, Pasadena, CA.ORCID 0000-0002-8184-7275
Sagar A PatelDepartment of Urology, Emory University, Atlanta, GA.ORCID 0000-0001-5174-2096

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Prostate Cancer Biomarker and Imaging Validation Alliance: Emory University, University of Alabama Birmingham, and University of Texas SouthwesternU01CA113913 · NCI · EMORY UNIVERSITY · PI Martin G. Sanda · 2005 to 2026
$16.4M
Emory Clinical Oncology Career Development Award K12 ProgramK12CA237806 · NCI · EMORY UNIVERSITY · PI DHODAPKAR, KAVITA MADHAV, RAMALINGAM, SURESH S · 2019 to 2023
$2.2M
NCI NIH HHS K12 CA237806NCI NIH HHS P30 CA008748NCI NIH HHS U01 CA113913
6 · The paper itself

Abstract

purposeBiopsy tissue-based genomic classifiers (GCs) for prostate cancer are commercially available tools to enhance prognostication. They may corroborate candidacy for active surveillance/watchful waiting (AS/WW) or identify men who are more likely to benefit from radiotherapy (RT) with androgen deprivation therapy (ADT). We analyze real-world use of GC and associations with clinical decision making. PATIENTS AND

methodsWe examined US commercial (n = 134,561) and Medicare (n = 68,431) insurance claims of men with newly diagnosed, localized prostate cancer between 2013 and 2022. We evaluated utilization of GCs over time and compared use of AS/WW, RT with or without ADT, radical prostatectomy (RP), or focal ablative therapy (FT) based on the receipt and type of GC.

resultsGC utilization increased from <1% to 17% in 8 years with a median payment of $3,001 (IQR, $0-3,873). Younger age, higher median household income, and high-deductible health insurance were associated with higher odds of receiving a GC (all

conclusionWe show contemporary, real-world GC utilization trends, costs, and associations with treatment patterns. Prospective trials are ongoing to validate GC-informed treatment, but US uptake has expanded and management is associated with the use and type of GC.

Indexed as

GenomicsHealth Care CostsPatient SelectionProstatic NeoplasmsAblation TechniquesAdultAndrogen AntagonistsBiopsyChemoradiotherapyHumansInsurance, HealthMaleMedicareMiddle AgedMolecular Diagnostic TechniquesPatient Acceptance of Health CareAndrogen Antagonists

Identifiers

PMID40834325
PMCPMC12370275

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Registered trials

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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.