Evidence map›Paper›PMID 39930910›Full record

ArticleCancer science2025

Germline Pathogenic Variants and Clinical Outcomes in Asian Patients With Breast Cancer.

Rui Kitadai, Shu Yazaki, Aya Kuchiba, Takashi Yamanaka, Sho Shiino, Chisako Yamauchi, Kenichi Harano, Motonobu Saito, Yosuke Hirotsu, Hisaki Aiba and 29 more

Abstract read
In one paragraph

Article in Cancer science, 2025. 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

39 authors.

Rui KitadaiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0478-9427
Shu YazakiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6141-9927
Aya KuchibaTeikyo University Graduate School of Public Health, Tokyo, Japan.
Takashi YamanakaDepartment of Breast Surgery and Oncology, Kanagawa Cancer Center, Yokohama, Japan.
Sho ShiinoDepartment of Breast Surgery, National Cancer Center Hospital, Tokyo, Japan.
Chisako YamauchiDepartment of Breast Surgery, National Cancer Center Hospital East, Chiba, Japan.
Kenichi HaranoDepartment of Experimental Therapeutics, National Cancer Center Hospital East, Chiba, Japan.
Motonobu SaitoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yosuke HirotsuGenome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.ORCID https://orcid.org/0000-0002-8002-834X
Hisaki AibaDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Teruhiko YoshidaDepartment of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
Ryuji HamamotoDivision of Medical AI Research and Development, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2632-1334
Chikako ShimizuDepartment of Breast and Medical Oncology, National Center for Global Health and Medicine, Tokyo, Japan.
Akihiko ShimomuraDepartment of Breast and Medical Oncology, National Center for Global Health and Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2557-8170
Yuki KojimaDepartment of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tatsunori ShimoiDepartment of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yukihide MomozawaLaboratory for Genotyping Development, Center for Integrative Medical Sciences, Yokohama, Japan.
Kazuki SudoDepartment of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4600-9428
Masayuki YoshidaDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Kuniko SunamiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7137-5649
Megumi HoriSchool of Nursing, University of Shizuoka, Shizuoka, Japan.
Kota KatanodaDivision of Population Data Science, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Yoko ShimadaDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Yuji YamashitaDepartment of Breast Surgery, National Cancer Center Hospital East, Chiba, Japan.
Takahiro KogawaDivision of Early Clinical Development for Cancer, Department of Advanced Medical Development, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Takeshi MurataDepartment of Breast Surgery, National Cancer Center Hospital, Tokyo, Japan.
Saori FujiwaraDepartment of Breast Surgery and Oncology, Kanagawa Cancer Center, Yokohama, Japan.
Yohei MiyagiMolecular Pathology and Genetics Division, Kanagawa Cancer Center Research Institute, Yokohama, Japan.
Hiroshi NakagomiDepartment of Obstetrics and Gynecology, Yamanashi Central Hospital, Yamanashi, Japan.ORCID https://orcid.org/0000-0002-0068-4487
Kazunoshin TachibanaDepartment of Breast Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Masao OmataDepartment of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.
Tohru OhtakeDepartment of Breast Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Akihiko SutoDepartment of Breast Surgery, National Cancer Center Hospital, Tokyo, Japan.
Tatsuya OnishiDepartment of Breast Surgery, National Cancer Center Hospital East, Chiba, Japan.
Yoichi NaitoDepartment of Experimental Therapeutics, National Cancer Center Hospital East, Chiba, Japan.ORCID https://orcid.org/0000-0002-8490-9064
Toshinari YamashitaDepartment of Breast Surgery and Oncology, Kanagawa Cancer Center, Yokohama, Japan.
Kan YonemoriDepartment of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7624-7611
Takashi KohnoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5371-706X
Kouya ShiraishiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5821-7400

Funding

Health Labour Sciences Research Grant 202108001BJapan Agency for Medical Research and Development JP15ck0106096 19cm0106605h0003 23ama2Japan Society for the Promotion of Science JP18K16292 20H03668 23H02955
6 · The paper itself

Abstract

Despite the importance of genetic testing for risk assessment and treatment in breast cancer, the prognostic impact of germline pathogenic variants (PVs), especially in Asian populations, is unclear. We assessed the impact of germline PVs in patients with early-stage breast cancer. This study included 7278 Japanese multihospital registry patients. PVs of ATM, BRCA1, BRCA2, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, and TP53 were evaluated. PV and non-PV carriers were matched by age, histology, and stage. Associations between PVs and survival were assessed. The primary outcome was invasive disease-free survival (IDFS). Secondary outcomes included relapse-free survival (RFS), overall survival, and breast cancer-specific survival. We identified 320 (4.4%) patients with BRCA1/2 PVs and 79 (1.1%) with PVs other than BRCA1/2 (non-BRCA1/2). A total of 360 patients (BRCA1/2, n = 289; non-BRCA1/2, n = 71) were matched to 720 noncarriers. Patients with BRCA1/2 PVs had significantly shorter 10-year IDFS (adjusted hazard ratio (aHR) = 2.15; 95% confidence interval (CI), 1.61-2.86; p < 0.001); and RFS (aHR = 1.74; 95% CI, 1.25-2.44; p = 0.001) than noncarriers. Among patients with hormone receptor-positive HER2-negative breast cancer, BRCA1/2 PV carriers exhibited significantly shorter 10-year IDFS than noncarriers, even those with stage I/II disease (total, aHR = 2.23; 95% CI, 1.55-3.23; p < 0.001, Stage I/II, aHR = 2.22; 95% CI, 1.43-3.44; p < 0.001). There was no significant difference in 10-year IDFS between the non-BRCA1/2 PV carrier and noncarrier groups (aHR = 1.40; 95% CI, 0.67-2.93; p = 0.37). Asian patients with breast cancer carrying germline BRCA1/2 PV, even those with a low recurrence risk, have significantly shorter 10-year IDFS than noncarriers.

Indexed as

Breast NeoplasmsGerm-Line MutationAdultAgedBRCA1 ProteinBRCA2 ProteinDisease-Free SurvivalEast Asian PeopleFemaleGenetic Predisposition to DiseaseGenetic TestingHumansMiddle AgedPrognosisBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBreast cancercancer predisposition geneshormone receptor‐positivepathogenic variantsprognosis

Identifiers

PMID39930910
PMCPMC11967260

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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.