Evidence map›Paper›PMID 35118230›Full record

ArticleJNCI cancer spectrum2022

Clinical Utility of Germline Genetic Testing in Japanese Men Undergoing Prostate Biopsy.

Shusuke Akamatsu, Naoki Terada, Ryo Takata, Hidefumi Kinoshita, Kimihiro Shimatani, Yukihide Momozawa, Michio Yamamoto, Harue Tada, Naoki Kawamorita, Shintaro Narita and 19 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in JNCI cancer spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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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

29 authors at 16 institutions in 1 country.

Shusuke AkamatsuDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-1394-7506
Naoki TeradaDepartment of Urology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Ryo TakataRIKEN Center for Integrative Medical Sciences, Laboratory for Cancer Genomics, Kanagawa, Japan.ORCID 0000-0002-4860-8942
Hidefumi KinoshitaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.
Kimihiro ShimataniDepartment of Urology, Hyogo College of Medicine, Hyogo, Japan.
Yukihide MomozawaLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
Michio YamamotoInstitute for Advancement of Clinical and Translational Science (iACT), Kyoto University Hospital, Kyoto, Japan.ORCID 0000-0003-1272-7090
Harue TadaInstitute for Advancement of Clinical and Translational Science (iACT), Kyoto University Hospital, Kyoto, Japan.ORCID 0000-0001-8634-5592
Naoki KawamoritaDepartment of Urology, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Shintaro NaritaDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Takuma KatoDepartment of Urology, Faculty of Medicine, Kagawa University, Kagawa, Japan.ORCID 0000-0003-2047-496X
Masahiro NittaDepartment of Urology, Tokai University School of Medicine, Kanagawa, Japan.
Shuya KandoriDepartment of Urology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.ORCID 0000-0003-4621-8470
Yusuke KoikeDepartment of Urology, Jikei University School of Medicine, Tokyo, Japan.
Johji InazawaDepartment of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Takahiro KimuraDepartment of Urology, Jikei University School of Medicine, Tokyo, Japan.ORCID 0000-0002-5673-1553
Hiroko KimuraDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0001-8071-6700
Takahiro KojimaDepartment of Urology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Toshiro TerachiDepartment of Urology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Mikio SugimotoDepartment of Urology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Tomonori HabuchiDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Yoichi AraiDepartment of Urology, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Shingo YamamotoDepartment of Urology, Hyogo College of Medicine, Hyogo, Japan.
Tadashi MatsudaDepartment of Urology and Andrology, Kansai Medical University, Osaka, Japan.
Wataru ObaraDepartment of Urology, School of Medicine, Iwate Medical University, Iwate, Japan.ORCID 0000-0003-2720-9640
Toshiyuki KamotoDepartment of Urology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Takahiro InoueDepartment of Nephro-Urologic Surgery and Andrology, Mie University Graduate School of Medicine, Mie, Japan.
Hidewaki NakagawaDepartment of Urology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Osamu OgawaDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kyoto University · JPUniversity of Miyazaki · JPUniversity of Tsukuba · JPAkita University · JPHyogo Medical University · JPIwate Medical University · JPJikei University School of Medicine · JPKagawa University · JPKansai Medical University · JPTohoku University · JPKyoto University Hospital · JPMie University · JPOkayama University · JPRIKEN Center for Integrative Medical Sciences · JPTokai University · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple common variants and also rare variants in monogenic risk genes such as Methods: A total of 1336 patients undergoing first prostate biopsy were included. PRS was calculated based on the genotype of 16 common variants, and sequencing of 8 prostate cancer-associated genes was performed by multiplex polymerase chain reaction based target sequencing. PRS was combined with clinical factors in logistic regression models to assess whether addition of PRS improves the prediction of biopsy positivity. Results: The top PRS decile was associated with an odds ratio of 4.10 (95% confidence interval = 2.46 to 6.86) with reference to the patients at average risk, and the estimated lifetime absolute risk approached 20%. Among the patients with prostate specific antigen 2-10 ng/mL who had prebiopsy magnetic resonance imaging, high PRS had an equivalent impact on biopsy positivity as a positive magnetic resonance imaging finding. Rare variants were detected in 19 (2.37%) and 7 (1.31%) patients with positive and negative biopsies, respectively, with Conclusions: Germline genetic testing could be clinically useful in both pre- and post-PSA screening settings.

Indexed as

Genetic VariationGerm-Line MutationAdultAgedAged, 80 and overArea Under CurveAtaxia Telangiectasia Mutated ProteinsBiopsy, NeedleConfidence IntervalsGenes, BRCA2Genetic TestingGenotypeHomeodomain ProteinsHumansJapanLogistic ModelsAtaxia Telangiectasia Mutated ProteinsATM protein, humanHomeodomain ProteinsHOXB13 protein, humanProstate-Specific Antigen

Identifiers

PMID35118230
PMCPMC8807580
OpenAlexW4205318283

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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.