Evidence map›Paper›PMID 40035318›Full record

ArticleCancer science2025

The Time Lag Associated With the Reclassification of Germline BRCA Variants' Pathogenicity Is Critical for Cancer Patients.

Tomomi Hayashi, Hiroyuki Matsubayashi, Yoshimi Kiyozumi

Abstract readCase ReportsLetter
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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Comprehensive evidence for the pathogenicity of theJournal of medical genetics · 2026
    Article
  2. Article
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

3 authors.

Tomomi HayashiDivision of Breast Surgery, Shizuoka Cancer Center, Nagaizumi, Japan.
Hiroyuki MatsubayashiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Nagaizumi, Japan.ORCID https://orcid.org/0000-0002-7050-2351
Yoshimi KiyozumiDivision of Genetic Medicine Promotion, Shizuoka Cancer Center, Nagaizumi, Japan.ORCID https://orcid.org/0000-0002-0816-9199

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The period for reclassifying the variants' pathogenicity is too long for patients with advanced or recurrent cancers with variants of uncertain significance that can be objectively re-evaluated to be (likely) pathogenic according to accumulated evidence. At present, we have three breast cancer patients with the germline variant BRCA2 c.7847C>T, which was genetically evaluated to be likely pathogenic by the paper in Cancer Science.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsGerm-Line MutationAdultFemaleGenetic Predisposition to DiseaseHumansMiddle AgedBRCA1 ProteinBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID40035318
PMCPMC12400043

What OpenQuestion holds

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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.