Evidence map›Paper›PMID 35087199›Full record

ArticleScientific reports2022

Precision cancer genome testing needs proficiency testing involving all stakeholders.

Masato Maekawa, Terumi Taniguchi, Kazuto Nishio, Kazuko Sakai, Kazuyuki Matsushita, Kaname Nakatani, Takayuki Ishige, Makoto Ikejiri, Hiroshi Nishihara, Kuniko Sunami and 18 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

28 authors at 13 institutions in 1 country.

Masato MaekawaDepartment of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan. mmaekawa@hama-med.ac.jp.
Terumi TaniguchiDepartment of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Kazuto NishioDepartment of Genome Biology, Kindai University Faculty of Medicine, Sayama, Japan.
Kazuko SakaiDepartment of Genome Biology, Kindai University Faculty of Medicine, Sayama, Japan.
Kazuyuki MatsushitaDepartment of Laboratory Medicine, Chiba University Hospital, Chiba, Japan.
Kaname NakataniDepartment of Clinical Laboratory, Mie University Hospital, Tsu, Japan.
Takayuki IshigeDepartment of Laboratory Medicine, Chiba University Hospital, Chiba, Japan.
Makoto IkejiriDepartment of Clinical Laboratory, Mie University Hospital, Tsu, Japan.
Hiroshi NishiharaGenomics Unit, Keio Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Kuniko SunamiDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Yasushi YatabeDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Kanako C HatanakaCenter for Development of Advanced Diagnostics, Hokkaido University Hospital, Sapporo, Japan.
Yutaka HatanakaCenter for Development of Advanced Diagnostics, Hokkaido University Hospital, Sapporo, Japan.
Yoshihiro YamamotoDepartment of Clinical Oncology, Kyoto University Hospital, Kyoto, Japan.
Keita FukuyamaDepartment of Clinical Oncology, Kyoto University Hospital, Kyoto, Japan.
Shinya OdaCancer Genetics Laboratory, Clinical Research Institute, National Hospital Organization, Kyushu Cancer Center, Fukuoka, Japan.
Kayoko SaitoInstitute of Medical Genetics, Tokyo Women's Medical Genetics, Tokyo, Japan.
Mamoru YokomuraInstitute of Medical Genetics, Tokyo Women's Medical Genetics, Tokyo, Japan.
Yuji KuboGenetic Analysis Department, Tsukiji Registered Clinical Laboratory, Riken Genesis Co., Ltd., National Cancer Center, Tokyo, Japan.
Hiroko SatoGenetic Analysis Department, Kawasaki Registered Clinical Laboratory, RIKEN Genesis Co., Ltd., Life Innovation Center, Kawasaki, Japan.
Yoshinori TanakaGenetic Analysis Department, Kawasaki Registered Clinical Laboratory, RIKEN Genesis Co., Ltd., Life Innovation Center, Kawasaki, Japan.
Misa FuchiokaGenetic & Pathology Department, SRL, Inc., Hachioji, Japan.
Tadashi YamasakiDevelopment of Clinical Genomics, BML Inc., Kawagoe, Japan.
Koichiro MatsudaMolecular Genetic Analysis Department, Advanced Technology Center, LSI Medience Corporation, Tokyo, Japan.
Kiyotaka KurachiSecond Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Kazuhiro FunaiFirst Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Satoshi BabaDepartment of Diagnostic Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Moriya IwaizumiDepartment of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Hamamatsu University School of Medicine · JPChiba University Hospital · JPHokkaido University Hospital · JPKawasaki Hospital · JPKindai University · JPKyoto University Hospital · JPMie University Hospital · JPTokyo National Hospital · JPTokyo Women's Medical University · JPHamamatsu University · JPKeio University · JPMedical & Biological Laboratories (Japan) · JPNational Hospital Organization Kyushu Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To implement precision oncology, analytical validity as well as clinical validity and utility are important. However, proficiency testing (PT) to assess validity has not yet been systematically performed in Japan. To investigate the quality of next-generation sequencing (NGS) platforms and cancer genome testing prevalent in laboratories, we performed pilot PT using patient samples. We prepared genomic DNA from the cancer tissue and peripheral blood of 5 cancer patients and distributed these to 15 laboratories. Most participating laboratories successfully identified the pathogenic variants, except for two closely located KRAS variants and 25 bp delins in EGFR. Conversely, the EGFR L858R variant was successfully identified, and the allele frequency was similar for all the laboratories. A high DNA integrity number led to excellent depth and reliable NGS results. By conducting this pilot study using patient samples, we were able to obtain a glimpse of the current status of cancer genome testing at participating laboratories. To enhance domestic cancer genome testing, it is important to conduct local PT and to involve the parties concerned as organizers and participants.

Indexed as

High-Throughput Nucleotide SequencingLaboratory Proficiency TestingNeoplasmsPrecision MedicineErbB ReceptorsFemaleGenetic TestingGenome, HumanHumansJapanMaleMutationPilot ProjectsProto-Oncogene Proteins p21(ras)Stakeholder ParticipationEGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID35087199
PMCPMC8795413
OpenAlexW4210480473

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.