Evidence map›Paper›PMID 39915020›Full record

ArticleBMJ open2025

Korean patients with hereditary cancer: a prospective multicentre cohort study protocol exploring psychosocial and health outcomes.

Jun-Kyu Kim, Mi-Ae Jang, Jong Eun Park, Dongju Won, Jung-Sook Ha, Kyoung-Bo Kim, Boyoung Park, Sun-Young Kong

Erratum issuedAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Jun-Kyu KimTargeted Therapy Branch, National Cancer Center, Goyang, Korea (the Republic of).ORCID http://orcid.org/0009-0000-3788-2092
Mi-Ae JangDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea (the Republic of).
Jong Eun ParkDepartment of Laboratory Medicine, Hanyang University Guri Hospital, Guri, Korea (the Republic of).ORCID http://orcid.org/0000-0001-9131-6518
Dongju WonDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea (the Republic of).
Jung-Sook HaDepartment of Laboratory Medicine, Keimyung University School of Medicine, Daegu, Korea (the Republic of).
Kyoung-Bo KimDepartment of Laboratory Medicine, Keimyung University School of Medicine, Daegu, Korea (the Republic of).
Boyoung Park *Department of Preventive Medicine, Hanyang University College of Medicine, Seoul, Korea (the Republic of).ORCID http://orcid.org/0000-0003-1902-3184
Sun-Young Kong *Department of Laboratory Medicine, National Cancer Center, Goyang, Korea (the Republic of) ksy@ncc.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAlthough genetic testing for hereditary cancers is increasing, data on health attitudes based on genetic pathogenicity are limited. This cohort study aims to establish three subcohorts based on genetic testing results to assess the health impact of genetic variations. This study evaluates changes in participant quality of life (QoL), unmet needs and mental health over time based on their genetic variant status. METHODS AND ANALYSIS: This prospective cohort study will recruit 1435 patients with suspected hereditary cancer who have undergone ETHICS AND DISSEMINATION: The study protocol was approved by all the Ethics Committees: the National Cancer Center IRB (NCC2023-0179), the Samsung Medical Center IRB (SMC2023-09-057), the Yonsei University Health System, Severance Hospital IRB (4-2023-0627), the Hanyang University Guri Hospital IRB (GURI2023-08-021) and the Keimyung University IRB (DSMC IRB 2024-05-048). The study outcomes will be disseminated through conference presentations, peer-reviewed publications and social media. TRIAL REGISTRATION NUMBER: KCT0009460.

Indexed as

NeoplasmsQuality of LifeAdultBRCA1 ProteinBRCA2 ProteinFemaleGenetic Predisposition to DiseaseGenetic TestingHigh-Throughput Nucleotide SequencingHumansMaleMental HealthMiddle AgedMulticenter Studies as TopicProspective StudiesRepublic of KoreaBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBreast tumoursCancer geneticsGENETICSGynaecological oncologyONCOLOGY

Identifiers

PMID39915020
PMCPMC11800292

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.