Evidence map›Paper›PMID 38767824›Full record

ReviewAdvances in therapy2024

Homologous Recombination Repair Gene Mutations in Prostate Cancer: Prevalence and Clinical Value.

Yu Fan, Zhenhua Liu, Yuke Chen, Zhisong He

Abstract readReview
In one paragraph

Review in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
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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

4 authors.

Yu FanDepartment of Urology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, China.
Zhenhua LiuGlobal Medical Affairs, MSD China, Shanghai, China.
Yuke ChenDepartment of Urology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, China.
Zhisong HeDepartment of Urology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, China. wyj7074@sohu.com.ORCID 0009-0004-9783-0859

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in our understanding of the molecular landscape of prostate cancer and the development of novel biomarker-driven therapies, the prognosis of patients with metastatic prostate cancer that is resistant to conventional hormonal therapy remains poor. Data suggest that a significant proportion of patients with metastatic castration-resistant prostate cancer (mCRPC) have mutations in homologous recombination repair (HRR) genes and may benefit from poly(ADP-ribose) polymerase (PARP) inhibitors. However, the adoption of HRR gene mutation testing in prostate cancer remains low, meaning there is a missed opportunity to identify patients who may benefit from targeted therapy with PARP inhibition, with or without novel hormonal agents. Here, we review the current knowledge regarding the clinical significance of HRR gene mutations in prostate cancer and discuss the efficacy of PARP inhibition in patients with mCRPC. This comprehensive overview aims to increase the clinical implementation of HRR gene mutation testing and inform future efforts in personalized treatment of prostate cancer.

Indexed as

MutationPoly(ADP-ribose) Polymerase InhibitorsProstatic Neoplasms, Castration-ResistantRecombinational DNA RepairHumansMalePrevalencePrognosisProstatic NeoplasmsPoly(ADP-ribose) Polymerase InhibitorsHomologous recombination repairPARP inhibitorsProstate cancer

Identifiers

PMID38767824
PMCPMC11133173

What OpenQuestion holds

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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.