Evidence map›Paper›PMID 35205755›Full record

ReviewCancers2022

Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers.

Roderick Clark, Jaime Herrera-Caceres, Miran Kenk, Neil Fleshner

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

4 authors at 2 institutions in 2 countries.

Roderick ClarkDivision of Urology, University of Toronto, Toronto, ON M5G 1X6, Canada.ORCID 0000-0001-7987-375X
Jaime Herrera-CaceresDepartment of Urology, Penn State Health, Hershey, PA 17033, USA.
Miran KenkDivision of Urology, University of Toronto, Toronto, ON M5G 1X6, Canada.
Neil FleshnerDivision of Urology, University of Toronto, Toronto, ON M5G 1X6, Canada.
University of Toronto · CAPenn State Milton S. Hershey Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer is a leading cause of death. Approximately one in eight men who are diagnosed with prostate cancer will die of it. Since there is a large difference in mortality between low- and high-risk prostate cancers, it is critical to identify individuals who are at high-risk for disease progression and death. Germline genetic differences are increasingly recognized as contributing to risk of lethal prostate cancer. The objective of this paper is to review prostate cancer management options for men with high-risk germline mutations.

methodsWe performed a review of the literature to identify articles regarding management of prostate cancer in individuals with high-risk germline genetic mutations.

resultsWe identified numerous publications regarding the management of prostate cancer among high-risk germline carriers, but the overall quality of the evidence is low.

conclusionsWe performed a review of the literature and compiled clinical considerations for the management of individuals with high-risk germline mutations when they develop prostate cancer. The quality of the evidence is low, and there is an immediate need for further research and the development of consensus guidelines to guide clinical practice for these individuals.

Indexed as

clinical managementgermline genetic mutationsprostate cancer

Identifiers

PMID35205755
PMCPMC8870148
OpenAlexW4213164681

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.