Evidence map›Paper›PMID 32923906›Full record

ArticleJCO precision oncology2020

Pathogenic Germline DNA Repair Gene and

Julie L Boyle, Andrew W Hahn, Ashley L Kapron, Wendy Kohlmann, Samantha E Greenberg, Timothy J Parnell, Craig C Teerlink, Benjamin L Maughan, Bing-Jian Feng, Lisa Cannon-Albright and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in JCO precision oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Julie L BoyleDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Andrew W HahnDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Ashley L KapronDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Wendy KohlmannHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Samantha E GreenbergHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Timothy J ParnellHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Craig C TeerlinkDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Benjamin L MaughanDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Bing-Jian FengHuntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Lisa Cannon-AlbrightDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Neeraj AgarwalDepartment of Internal Medicine, University of Utah, Salt Lake City, UT.
Kathleen A CooneyDepartment of Medicine and the Duke Cancer Institute, Duke University School of Medicine, Durham, NC.
University of Utah · USHuntsman Cancer Institute · USDuke University · USGeorge E. Wahlen Department of VA Medical Center · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
NCATS NIH HHS UL1 TR002538NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

purposeGermline mutations in DNA repair (DR) genes and susceptibility genes PATIENTS AND

methodsTo evaluate the frequency of pathogenic/likely pathogenic germline variants (PVs/LPVs) in men with mPC, this study sequenced 38 DR genes,

resultsAll pathogenic variants were found in men self-reported as white, with a carrier frequency of 8.5% (DR genes, 7.3%;

conclusionThese findings demonstrate a lower prevalence of germline PVs/LPVs in an unselected, predominantly white mPC cohort than previously reported, which may have implications for the design of clinical trials testing targeted therapies. Larger studies in broad and diverse populations are needed to more accurately define the prevalence of germline mutations in men with mPC.

Identifiers

PMID32923906
PMCPMC7446531
OpenAlexW3010642163

What OpenQuestion holds

Textmetadata
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.