Evidence map›Paper›PMID 42410220›Full record

ArticleJournal of human genetics2026

Towards sustainable hereditary breast and ovarian cancer surveillance: insights from a single-center survey.

Yumiko Goto, Tomoko Seki, Daisuke Nakato, Kohei Nakamura, Tomoko Yoshihama, Masayuki Tanaka, Ikumi Ono, Kumiko Misu, Yusuke Kobayashi, Kenta Masuda and 3 more

Abstract read
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In one paragraph

Article in Journal of human genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Yumiko GotoCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Tomoko SekiCenter for Hereditary Breast and Ovarian Cancer Syndrome, Keio University Hospital, Tokyo, Japan.
Daisuke NakatoCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Kohei NakamuraCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Tomoko YoshihamaCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Masayuki TanakaCenter for Hereditary Breast and Ovarian Cancer Syndrome, Keio University Hospital, Tokyo, Japan.
Ikumi OnoCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Kumiko MisuCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Yusuke KobayashiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Kenta MasudaCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Hiromasa TakaishiCenter for Preventive Medicine, Keio University School of Medicine, Tokyo, Japan.
Wataru YamagamiCenter for Hereditary Breast and Ovarian Cancer Syndrome, Keio University Hospital, Tokyo, Japan.
Kenjiro KosakiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan. kkosaki@keio.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary breast and ovarian cancer (HBOC) syndrome, caused by pathogenic variants in BRCA1 or BRCA2, is associated with increased risks of breast, ovarian, pancreatic, and prostate cancers. Although long-term, multi-organ surveillance is recommended, real-world data on its implementation in Japan remain limited. We conducted a web-based cross-sectional survey among 274 individuals registered for a hybrid public lecture at Keio University Hospital in 2024; 121 responded (44.2%). Respondents included HBOC carriers, healthcare professionals, and the general public. Among 66 carriers, 57 were affected and 9 were unaffected. Although the sample size is small, surveillance uptake was high among affected carriers (89.5%). Approximately half of affected carriers undergoing surveillance reported satisfaction, while nearly half underwent surveillance at multiple institutions, suggesting fragmented care. Across all groups including healthcare professionals and the general public, the most acceptable annual cost was less than 50,000 yen. Healthcare professionals identified interdepartmental coordination and shortages of genetic specialists as major challenges. These exploratory findings suggest that affordability, convenience, interdepartmental and interfacility coordination, and the availability of genetic medicine professionals may be important considerations in efforts to develop sustainable HBOC surveillance systems in Japan.

Indexed as

Hereditary Breast and Ovarian Cancer SyndromeOvarian NeoplasmsAdultAgedBRCA1 ProteinBRCA2 ProteinCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseGenetic TestingHumansJapanMaleMiddle AgedPopulation SurveillanceSurveys and QuestionnairesBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

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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.