Evidence map›Paper›PMID 34244736›Full record

ArticleJapanese journal of clinical oncology2021

Sharing genetic test results of germline pathogenic variants of hereditary cancer with relatives: A single-center cross-sectional study.

Naomi Fukuzaki, Yoshimi Kiyozumi, Satomi Higashigawa, Yasue Horiuchi, Maki Mizuguchi, Hiroyuki Matsubayashi, Seiichiro Nishimura, Keita Mori, Akifumi Notsu, Izumi Suishu and 5 more

Abstract read
In one paragraph

Article in Japanese journal of clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

15 authors.

Naomi FukuzakiDepartment of Nursing, Shizuoka Cancer Center Hospital, Shizuoka, Japan.ORCID 0000-0002-6112-4176
Yoshimi KiyozumiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Shizuoka, Japan.
Satomi HigashigawaDepartment of Nursing, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Yasue HoriuchiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Shizuoka, Japan.
Maki MizuguchiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Shizuoka, Japan.
Hiroyuki MatsubayashiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Shizuoka, Japan.
Seiichiro NishimuraDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Shizuoka, Japan.
Keita MoriClinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.
Akifumi NotsuClinical Research Center, Shizuoka Cancer Center, Shizuoka, Japan.
Izumi SuishuDepartment of Nursing, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Sumiko OhnamiShizuoka Cancer Center Research Institute, Shizuoka, Japan.
Masatoshi KusuharaShizuoka Cancer Center Research Institute, Shizuoka, Japan.
Ken YamaguchiShizuoka Cancer Center, Shizuoka, Japan.
Ardith Z DoorenbosDepartment of Biobehavioral Nursing Science, College of Nursing, University of Illinois Chicago, Chicago, USA.
Yuko TakedaGraduate School of Health Management, Keio University, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to determine whether Japanese cancer patients share test results of germline pathogenic variants of hereditary cancer with their relatives.

methodsThis single-center cross-sectional study enrolled 21 Japanese patients who received results of germline pathogenic variants of hereditary cancer at least 6 months prior.

resultsAll patients shared their test results with at least one relative, with the following sharing rates: 85.7% for first-degree relatives, 10% for second-degree relatives and 8.3% for third-degree relatives. Patients most commonly shared the information with their children aged >18 years (86.7%), followed by their siblings (73.6%), spouses (64.7%) and parents (54.5%). Three categories were extracted from qualitative analysis: 'characteristics of my cancer', 'knowledge and caution about inheritability' and 'utilization of medical care.'

conclusionsThe rate of test result sharing with first-degree relatives was comparable with those in Europe and the USA. Patients with germline pathogenic variants also tended to share their test results more with their children and siblings than with their parents. Informing their relatives of the results was suggestive of the motivation to influence their relatives' health outcome and contribute to the well-being of their children and siblings.

Indexed as

Genetic Predisposition to DiseaseNeoplasmsChildCross-Sectional StudiesGenetic TestingGerm CellsGerm-Line MutationHumansfamilygenetic testinggerm-line mutationhereditaryneoplastic syndromes

Identifiers

PMID34244736
PMCPMC8491536

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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.