Evidence map›Paper›PMID 31969336›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Farzana A Faisal, Sanjana Murali, Harsimar Kaur, Thiago Vidotto, Liana B Guedes, Daniela Correia Salles, Vishal Kothari, Jeffrey J Tosoian, Sumin Han, Daniel H Hovelson and 6 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Subclonal Complete Loss of CDKN1B as a Common Genomic Alteration in Prostate Cancer: Associations With Race and Prostate Cancer Outcomes.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2026
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  17. Genomic evidence suggests that cutaneous neuroendocrine carcinomas can arise from squamous dysplastic precursors.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  18. Review
  19. Review
  20. FOXA1 in prostate cancer.Asian journal of andrology
    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

16 authors at 4 institutions in 1 country.

Farzana A FaisalBrady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sanjana MuraliDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Harsimar KaurDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Thiago VidottoDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-7268-4494
Liana B GuedesDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Daniela Correia SallesDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Vishal KothariPolsky Urologic Cancer Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Jeffrey J TosoianDepartment of Urology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-7614-9931
Sumin HanMichigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
Daniel H HovelsonMichigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
Kevin HuDepartment of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan.
Daniel E SprattRogel Cancer Center, University of Michigan Medical School, Ann Arbor, Michigan.
Alexander S BarasDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Scott A Tomlins *Department of Urology, University of Michigan Medical School, Ann Arbor, Michigan. tlotan1@jhmi.edu e-schaeffer@northwestern.edu tomlinss@med.umich.edu.
Edward M Schaeffer *Polsky Urologic Cancer Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois. tlotan1@jhmi.edu e-schaeffer@northwestern.edu tomlinss@med.umich.edu.
Tamara L Lotan *Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland. tlotan1@jhmi.edu e-schaeffer@northwestern.edu tomlinss@med.umich.edu.
Johns Hopkins University · USUniversity of Michigan · USNorthwestern University · USMichigan Center for Translational Pathology · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
TRANSGENIC MODELS FOR PROSTATE CANCER AND AUTOIMMUNITYP50CA058236 · NCI · JOHNS HOPKINS UNIVERSITY · PI DENMEADE, SAMUEL R · 1992 to 2020
$43.9M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Timothy Dess · 2014 to 2026
$27.6M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Multidiciplinary Integrative Genomic Approach to Distinguish Lethal from Indolent Prostate Cancer in Men of Europena and African AncestryU01CA196390 · NCI · JOHNS HOPKINS UNIVERSITY · PI DE MARZO, ANGELO MICHAEL, PIENTA, KENNETH J. · 2015 to 2020
$5.8M
Exploiting drivers of androgen receptor signaling negative prostate cancer for prR01CA183857 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TOMLINS, SCOTT A · 2014 to 2018
$1.6M
NCI NIH HHS P30 CA006973NCI NIH HHS P50 CA058236NCI NIH HHS P50 CA180995NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA183857NCI NIH HHS U01 CA196390
6 · The paper itself

Abstract

purposeThe potential biological determinants of aggressive prostate cancer in African American (AA) men are unknown. Here we characterize prostate cancer genomic alterations in the largest cohort to date of AA men with clinical follow-up for metastasis, with the aim to elucidate the key molecular drivers associated with poor prognosis in this population. EXPERIMENTAL

designTargeted sequencing was retrospectively performed on 205 prostate tumors from AA men treated with radical prostatectomy (RP) to examine somatic genomic alterations and percent of the genome with copy-number alterations (PGA). Cox proportional hazards analyses assessed the association of genomic alterations with risk of metastasis.

resultsAt RP, 71% (145/205) of patients had grade group ≥3 disease, and 49% (99/202) were non-organ confined. The median PGA was 3.7% (IQR = 0.9%-9.4%) and differed by pathologic grade (

conclusionsOverall, PGA, somatic

Indexed as

Gene DeletionBiomarkers, TumorBlack or African AmericanCyclin-Dependent Kinase Inhibitor p27Follow-Up StudiesGenomicsHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalPrognosisProstatectomyProstatic NeoplasmsRetrospective StudiesSurvival RateBiomarkers, TumorCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27

Identifiers

PMID31969336
PMCPMC7269813
OpenAlexW3002751854

What OpenQuestion holds

Textmetadata
LicenceTDM
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.