Evidence map›Paper›PMID 39885596›Full record

ArticleJournal of ovarian research2025

Whole exome sequencing-based homologous recombination deficiency test for epithelial ovarian cancer.

Ying-Cheng Chiang, Hsien-Neng Huang, Kuan-Ting Kuo, Wuh-Liang Hwu, Po-Han Lin

Abstract read
In one paragraph

Article in Journal of ovarian research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 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

5 authors.

Ying-Cheng ChiangDepartment of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei City, Taiwan.
Hsien-Neng HuangDepartment of Pathology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, Taiwan.
Kuan-Ting KuoDepartment of Pathology, College of Medicine, National Taiwan University, Taipei City, Taiwan.
Wuh-Liang HwuDepartment of Pediatrics, National Taiwan University Hospital, Taipei City, Taiwan.
Po-Han LinDepartment of Medical Genetics, National Taiwan University Hospital, 19F, No. 8, Chung-Shan South Road, Taipei City, Taiwan. pohanlin01@ntu.edu.tw.

Funding

Takeda Pharmaceuticals Taiwan, Ltd. 201807116RINA
6 · The paper itself

Abstract

backgroundThe homologous recombination deficiency (HRD) test is an important tool for identifying patients with epithelial ovarian cancer (EOC) benefit from the treatment with poly(adenosine diphosphate-ribose) polymerase inhibitor (PARPi). Using whole exome sequencing (WES)-based platform can provide information of gene mutations and HRD score; however, the clinical value of WES-based HRD test was less validated in EOC.

methodsWe enrolled 40 patients with EOC in the training cohort and 23 in the validation cohort. The WES-based HRD score was calculated using the scarHRD software. We first evaluated the concordance of the HRD status defined by the Myriad MyChoice CDx and then assessed the value of HRD on clinical prognosis in patients with EOC.

resultsThe HRD score defined by the WES-based test was positively correlated with that of the Myriad MyChoice

conclusionThe WES-based test is a potential option for determining the HRD status in EOC patients, and desires for further validation in large-scale cohorts.

Indexed as

Carcinoma, Ovarian EpithelialExome SequencingHomologous RecombinationOvarian NeoplasmsAdultAgedFemaleHumansMiddle AgedMutationPrognosisEpithelial ovarian cancerHomologous recombination deficiency testscarHRDWhole-exome sequencing

Identifiers

PMID39885596
PMCPMC11780812

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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.