Evidence map›Paper›PMID 40926019›Full record

ArticleJournal of human genetics2026

Germline pathogenic variants detected by GenMineTOP: insight from a nationwide tumor/normal paired comprehensive genomic profiling test, in Japan.

Eri Habano, Miho Ogawa, Kousuke Watanabe, Nana Akiyama, Hyangri Chang, Mirei Ka, Aya Shinozaki-Ushiku, Masahiko Tanabe, Masakazu Akahori, Toshimitsu Ichijo and 5 more

Abstract read
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. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Review
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  6. Article
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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.

Eri HabanoDivision of Integrative Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Miho OgawaNext-Generation Precision Medicine Development Laboratory, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kousuke WatanabeNext-Generation Precision Medicine Development Laboratory, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Nana AkiyamaDepartment of Clinical Genomics, The University of Tokyo Hospital, Tokyo, Japan.
Hyangri ChangDepartment of Clinical Genomics, The University of Tokyo Hospital, Tokyo, Japan.
Mirei KaDivision of Integrative Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0009-0001-8950-8948
Aya Shinozaki-UshikuDivision of Integrative Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Masahiko TanabeDepartment of Breast and Endocrine Surgery, The University of Tokyo Hospital, Tokyo, Japan.
Masakazu AkahoriKONICAMINOLTA INC., Tokyo, Japan.
Toshimitsu IchijoKONICAMINOLTA INC., Tokyo, Japan.
Shuichi TsutsumiResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Kenji TatsunoResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Hiroyuki AburataniResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-0438-1544
Hidenori KageDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Katsutoshi OdaDivision of Integrative Genomics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. katsutoshi-tky@umin.ac.jp.

Funding

Japan Agency for Medical Research and Development (AMED) JP21km0908001MEXT | Japan Society for the Promotion of Science (JSPS) 24K02584
6 · The paper itself

Abstract

Comprehensive genomic profiling (CGP) expands treatment options for solid tumor patients and identifies hereditary cancers. However, in Japan, confirmatory tests have been conducted in only 31.6% of patients with presumed germline pathogenic variants (GPVs) detected through tumor-only testing. Paired tumor-normal analysis enables differentiation between somatic and germline variants. GenMineTOP, covered by Japan's national health insurance since August 2023, analyzes paired samples and reports GPVs in 40 genes. This study provides an initial characterization of GPVs based on clinical findings collected during the first year of GenMineTOP implementation. We analyzed 1356 solid tumor patients who underwent GenMineTOP testing in the Center for Cancer Genomics and Advanced Therapeutics (C-CAT) database between August 2023 and July 2024, focusing on GPV detection rates, gene distribution, and comparisons with other CGP tests. Among the analyzed cancer types, GenMineTOP had a higher proportion of CNS/brain, soft tissue, bone, and head and neck cancers compared to other CGP tests. GPVs were detected in 73 patients (5.4%), with 38.2% classified as off-tumor. HR-related GPVs (ATM, BRCA1, BRCA2, BRIP1, PALB2, RAD51C, RAD51D) were found in both males (median age: 69) and females (median age: 54). Among males, 57.9% were aged 65 or older. GPVs may be detected in any cancer patients, including those with off-tumor findings, particularly in older male patients, especially in HR-related genes. These findings support the use of paired CGP to improve the diagnosis of hereditary cancers that could otherwise remain undetected.

Indexed as

Germ-Line MutationNeoplasmsAdultAgedAged, 80 and overChildFemaleGenetic Predisposition to DiseaseGenetic TestingGenomicsHumansJapanMaleMiddle AgedYoung Adult

Identifiers

PMID40926019
PMCPMC12689426

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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.