Evidence map›Paper›PMID 39383006›Full record

ArticleUrology practice2025

Detection of Germline Variants in Patients With Localized and Metastatic Prostate Cancer Through Guideline-Based Testing.

Sophia M Abusamra, Marissa A Solorzano, Jake Quarles, Mallory Luke, Milan Patel, Randy Vince, Ralph Jiang, Joshua Volin, Michelle F Jacobs, Samuel D Kaffenberger and 10 more

Abstract read
In one paragraph

Article in Urology practice, 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. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Sophia M AbusamraDepartment of Urology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-9588-5005
Marissa A SolorzanoDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Jake QuarlesMichigan Institute of Urology, Troy, Michigan.
Mallory LukeDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Milan PatelDepartment of Urology, Loyola University Medical Center, Maywood, Illinois.
Randy VinceDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Ralph JiangDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan.
Joshua VolinDepartment of Diagnostic Radiology and Imaging Science, Emory University School of Medicine, Atlanta, Georgia.
Michelle F JacobsOakland University William Beaumont School of Medicine, Beaumont Hospital, Royal Oak, Michigan.
Samuel D KaffenbergerDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Simpa S SalamiDepartment of Urology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-7461-7079
Phillip PalmbosDepartment of Internal Medicine, Division of Genetic Medicine, University of Michigan, Ann Arbor, Michigan.
Megan E V CaramDepartment of Internal Medicine, Division of Genetic Medicine, University of Michigan, Ann Arbor, Michigan.
Brent K HollenbeckDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Ganesh S PalapattuDepartment of Urology, University of Michigan, Ann Arbor, Michigan.
Sofia D MerajverDepartment of Internal Medicine, Hematology/Oncology Division, University of Michigan Medical School, Ann Arbor, Michigan.
Elena M StoffelDepartment of Internal Medicine, Division of Genetic Medicine, University of Michigan, Ann Arbor, Michigan.
Jason HafronMichigan Institute of Urology, Troy, Michigan.
Todd M MorganDepartment of Urology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-1140-0603
Zachery R ReichertDepartment of Urology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-0356-8796

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
Determining the clinical impact of gene expression testing in localized prostate cancerR01CA240991 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORGAN, TODD M., SPRATT, DANIEL EIDELBERG · 2019 to 2024
$3.1M
Mechanism and Therapeutic Targeting of TRIM29-mediated Invasion in Bladder CancerR37CA273138 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PHILLIP L PALMBOS · 2022 to 2026
$2.2M
NCI NIH HHS P30 CA046592NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA240991NCI NIH HHS R37 CA273138
6 · The paper itself

Abstract

introductionThere is increasing awareness that patients with prostate cancer frequently harbor germline variants that may carry important implications for them and their family members. Given the variable clinical guidelines, there remains a need to better understand which patients with prostate cancer are likely to harbor pathogenic or likely pathogenic (P/LP) germline variants. We sought to understand factors associated with P/LP germline variants in patients with metastatic or localized prostate cancer qualifying for National Comprehensive Cancer Network genetic testing criteria.

methodsPatients diagnosed with prostate cancer were offered genetic testing in accordance with National Comprehensive Cancer Network guidelines. Patient-level factors, including demographic, clinical, and pathologic data, were tracked in a prospectively collected registry. The association of the presence of a P/LP variant in germline testing results with patient-level factors was assessed using univariate and multivariate logistic regression. Variables were tested for overall significance with χ

resultsFive hundred five patients underwent germline testing and had clinical data available. Rates of P/LP germline variants were 7.6% (20/264) in patients with metastatic disease and 11.2% (27/241) in patients with localized disease. The most prevalent P/LP variants were

conclusionsIn this cohort of patients undergoing guideline-informed germline testing, P/LP germline variants were found in similar proportions across all age ranges and clinical characteristics. Only age at genetic testing for patients with metastatic disease was demonstrated to be predictive of the presence of a P/LP germline variant, highlighting the challenges associated with refining current clinical testing guidelines.

Indexed as

Genetic TestingGerm-Line MutationPractice Guidelines as TopicProstatic NeoplasmsAdultAgedAged, 80 and overCheckpoint Kinase 2Genetic Predisposition to DiseaseHomeodomain ProteinsHumansMaleMiddle AgedNeoplasm MetastasisCheckpoint Kinase 2CHEK2 protein, humanHomeodomain ProteinsHOXB13 protein, humangenetic testinggermline mutationprostatic neoplasms

Identifiers

PMID39383006
PMCPMC11658803

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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.