Evidence map›Paper›PMID 36804482›Full record

ArticleJournal of human genetics2023

Management of patients with presumed germline pathogenic variant from tumor-only genomic sequencing: A retrospective analysis at a single facility.

Maako Kawamura, Hidekazu Shirota, Tetsuya Niihori, Keigo Komine, Masanobu Takahashi, Shin Takahashi, Eisaku Miyauchi, Hidetaka Niizuma, Atsuo Kikuchi, Hiroshi Tada and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

20 authors at 3 institutions in 1 country.

Maako KawamuraPersonalized Medicine Center, Tohoku University Hospital, Sendai, Japan.
Hidekazu ShirotaDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan. hidekazu.shirota.e1@tohoku.ac.jp.
Tetsuya NiihoriDepartment of Medical Genetics, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID http://orcid.org/0000-0002-2118-9776
Keigo KomineDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan.
Masanobu TakahashiDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan.
Shin TakahashiDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan.
Eisaku MiyauchiDepartment of Respiratory Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hidetaka NiizumaDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Atsuo KikuchiDepartment of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.ORCID http://orcid.org/0000-0003-1002-8739
Hiroshi TadaDepartment of Breast and Endocrine Surgical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Muneaki ShimadaDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Sendai, Japan.
Naoki KawamoritaDepartment of Urology, Tohoku University School of Medicine, Sendai, Japan.
Masayuki KanamoriDepartment of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan.
Ikuko SugiyamaPersonalized Medicine Center, Tohoku University Hospital, Sendai, Japan.
Mari TsubataDepartment of Medical Genetics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hitotshi IchikawaDepartment of Clinical Genomics, National Cancer Center Research Institute, Tokyo, Japan.ORCID http://orcid.org/0000-0003-0142-2240
Jun YasudaDivision of Molecular Cellular Oncology, Miyagi Cancer Center Research Institute, Natori, Japan.ORCID http://orcid.org/0000-0002-3887-6871
Toru FurukawaDepartment of Investigative Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID http://orcid.org/0000-0002-1083-2324
Yoko AokiDepartment of Medical Genetics, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID http://orcid.org/0000-0002-1194-6972
Chikashi IshiokaDepartment of Clinical Oncology, Tohoku University Hospital, Sendai, Japan. chikashi@tohoku.ac.jp.
Tohoku University · JPTohoku University Hospital · JPMiyagi Prefectural Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer treatment is increasingly evolving toward personalized medicine, which sequences numerous cancer-related genes and identifies therapeutic targets. On the other hand, patients with germline pathogenic variants (GPV) have been identified as secondary findings (SF) and oncologists have been urged to handle them. All SF disclosure considerations for patients are addressed and decided at the molecular tumor boards (MTB) in the facility. In this study, we retrospectively summarized the results of all cases in which comprehensive genomic profiling (CGP) test was conducted at our hospital, and discussed the possibility of presumed germline pathogenic variants (PGPV) at MTB. MTB recommended confirmatory testing for 64 patients. Informed consent was obtained from attending physicians for 53 of them, 30 patients requested testing, and 17 patients tested positive for a confirmatory test. Together with already known variants, 4.5 % of the total confirmed in this cohort. Variants verified in this study were BRCA1 (n = 12), BRCA2 (n = 6), MSH2 (n = 2), MSH6 (n = 2), WT1 (n = 2), TP53, MEN1, CHEK2, MLH1, TSC2, PTEN, RB1, and SMARCB1. There was no difference in the tumor's VAF between confirmed positive and negative cases for variants determined as PGPV by MTB. Current results demonstrate the actual number of cases until confirmatory germline test for patients with PGPV from tumor-only CGP test through the discussion at the MTB. The practical results at this single facility will serve as a guide for the management of the selection and distribution of SF in the genome analysis.

Indexed as

Germ-Line MutationNeoplasmsGenes, BRCA2GenomicsHumansRetrospective Studies

Identifiers

PMID36804482
OpenAlexW4321377498

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.