Evidence map›Paper›PMID 39762492›Full record

ArticleScientific reports2025

Importance of EQA/PT for the detection of genetic variants in comprehensive cancer genome testing.

Kazuyuki Matsushita, Takayuki Ishige, Kousuke Watanabe, Toshiaki Akahane, Akihide Tanimoto, Michiko Yoshimoto, Munekazu Yamakuchi, Teruto Hashiguchi, Yoshinaga Okugawa, Makoto Ikejiri and 11 more

Abstract read
In one paragraph

Article in Scientific reports, 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

21 authors.

Kazuyuki MatsushitaDepartment of Laboratory Medicine, Chiba University Hospital, 1-8-1 Inohana Chuo-ku, Chiba, 260-8670, Japan. kmatsu@faculty.chiba-u.jp.
Takayuki IshigeDepartment of Laboratory Medicine, Chiba University Hospital, 1-8-1 Inohana Chuo-ku, Chiba, 260-8670, Japan.
Kousuke WatanabeDepartment of Clinical Laboratory, The University of Tokyo, Tokyo, Japan.
Toshiaki AkahaneDepartment of Pathology, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Akihide TanimotoDepartment of Pathology, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Michiko YoshimotoApplication support development, Global Management Division, Sysmex Corporation, Kobe, Japan.
Munekazu YamakuchiDepartment of Laboratory and Vascular Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Teruto HashiguchiDepartment of Laboratory and Vascular Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Yoshinaga OkugawaDepartment of Genomic Medicine, Mie University Hospital, Tsu, 514-8507, Japan.
Makoto IkejiriDepartment of Clinical Laboratory, Mie University Hospital, Tsu, 514-8507, Japan.
Toshikazu YamaguchiBML, Inc., 1361-1, Matoba, Kawagoe-shi, Saitama, 350-1101, Japan.
Tadashi YamasakiBML, Inc., 1361-1, Matoba, Kawagoe-shi, Saitama, 350-1101, Japan.
Mayu TakedaDepartment of Medical Research for Intractable Diseases, Fujita Health University, Toyoake, Japan.
Masaaki HibiAdvanced Medical Care Testing Department, SRL Genomics Division, SRL, Inc., Tokyo, Japan.
Naoki AkiyamaLab Assay Business, LS Business, Sysmex Corporation, Kobe, Japan.
Kaho ShimizuLab Assay Business, LS Business, Sysmex Corporation, Kobe, Japan.
Naonori HashimotoLab Assay Business, LS Business, Sysmex Corporation, Kobe, Japan.
Hiroko SatoGenetic Analysis Department, Kawasaki Registered Clinical Laboratory, Riken Genesis Co., Ltd., Kanagawa, Japan.
Yoshinori TanakaBioinformatics Department, Kawasaki Registered Clinical Laboratory, Riken Genesis Co., Ltd., Kanagawa, Japan.
Fumie AmariGenetic Analysis Department, Tsukiji Registered Clinical Laboratory, Riken Genesis Co., Ltd., Tokyo, Japan.
EQA working group of Japan Association for Clinical Laboratory Science(JACLS)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comprehensive genomic profiling (CGP) is increasingly used as a clinical laboratory test and being applied to cancer treatment; however, standardization and external quality assessments (EQA) have not been fully developed. This study performed cost-effective EQA and proficiency tests (PT) for CGP testing among multiple institutions those belong to the EQA working group of Japan Association for Clinical Laboratory Science (JACLS). This study revealed that preanalytical processes, such as derived nucleic acids (NA) extraction from formalin fixed paraffine embedded (FFPE) samples, are critical. First, EQA with extracted DNA from cell lines showed a detection rate of 100% (9 out of 9) in KRAS (c.38G > A; p.G13D), PIK3CA (p.H1047R), and B-Raf proto-oncogene, serine/threonine kinase (BRAF) (c.1799 T > A; p.V600E) in cases of > 10% variant allele frequency (VAF). However, BRAF (c.1799 T > A; p.V600E) detection decreased to 67% (6 out of 9) for a VAF of 4.9%. Second, when DNA was extracted from FFPE samples, pathogenic variants and variants with companion diagnostic indications were detected in all 10 participating laboratories. Each variant had < 20% VAFs on average (8.1-19.1%) and wide variability among laboratories was observed (relative standard deviation, 13-60%). Nonetheless, BRAF (c.1798_1799delinsAA; p.V600K) of 8.1% VAF, EGFR (c.2235_2249del; p.E746_A750del) of 9.7% VAF, and EGFR (c.2254_2277del; p.S752_I759del) of 9.8% VAF were detected with 70% (7/10), 70% (7/10), and 60% (6/10) frequency, respectively. Therefore, 10% VAF in pre-analytic processing for DNA extraction from FFPE was critical for variant detection in CGP analysis. Further, incorrect results were reported in case independent variant calling of BRAF; c.1798_1799delinsAA (p.V600K) was mistakenly interpreted as c.1798G > A, and c.1799 T > A was on the other strand. In conclusion, the EQA/PT among 10 institutes with common samples revealed the importance of VAF in pre-analysis and helped us understand the significance of the pipeline and common pitfalls usually ignored by the internal quality control in a single institute.

Indexed as

NeoplasmsCell Line, TumorGenetic TestingGenetic VariationGenomicsHumansLaboratory Proficiency TestingMutationProto-Oncogene MasProto-Oncogene Proteins B-rafMAS1 protein, humanProto-Oncogene MasProto-Oncogene Proteins B-rafComprehensive cancer genome testingExternal quality assessment (EQA)Genetic variantsNGSProficiency testing (PT)

Identifiers

PMID39762492
PMCPMC11704004

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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.