Evidence map›Paper›PMID 37189577›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Analytical Performance of a Highly Sensitive System to Detect Gene Variants Using Next-Generation Sequencing for Lung Cancer Companion Diagnostics.

Kikuya Kato, Jiro Okami, Harumi Nakamura, Keiichiro Honma, Yoshiharu Sato, Seiji Nakamura, Yoji Kukita, Shin-Ichi Nakatsuka, Masahiko Higashiyama

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Review
  10. Observational
  11. Retrospective Analysis to Optimize the Detection ofDiagnostics (Basel, Switzerland) · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Frontiers in oncology · 2022
    Article
  18. SuccessfulCase reports in oncology
    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

9 authors at 3 institutions in 1 country.

Kikuya KatoLaboratory of Medical Genomics, Nara Institute of Science and Technology, Nara 630-0192, Japan.ORCID 0000-0003-1863-6253
Jiro OkamiDepartment of General Thoracic Surgery, Osaka International Cancer Institute, Osaka 540-0008, Japan.
Harumi NakamuraLaboratory of Genomic Pathology, Osaka International Cancer Institute, Osaka 540-0008, Japan.ORCID 0000-0003-4476-8794
Keiichiro HonmaDepartment of Diagnostic Pathology and Cytology, Osaka International Cancer Institute, Osaka 540-0008, Japan.ORCID 0000-0001-5193-5891
Yoshiharu SatoDNA Chip Research Inc., Tokyo 105-0022, Japan.
Seiji NakamuraLaboratory of Medical Genomics, Nara Institute of Science and Technology, Nara 630-0192, Japan.
Yoji KukitaLaboratory of Medical Genomics, Nara Institute of Science and Technology, Nara 630-0192, Japan.
Shin-Ichi NakatsukaDepartment of Diagnostic Pathology and Cytology, Osaka International Cancer Institute, Osaka 540-0008, Japan.
Masahiko HigashiyamaDepartment of General Thoracic Surgery, Osaka International Cancer Institute, Osaka 540-0008, Japan.
Osaka International Cancer Institute · JPNara Institute of Science and Technology · JPDNA Chip Research (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent increase in the number of molecular targeted agents for lung cancer has led to the demand for the simultaneous testing of multiple genes. Although gene panels using next-generation sequencing (NGS) are ideal, conventional panels require a high tumor content, and biopsy samples often do not meet this requirement. We developed a new NGS panel, called compact panel, characterized by high sensitivity, with detection limits for mutations of 0.14%, 0.20%, 0.48%, 0.24%, and 0.20% for

Indexed as

companion diagnosticsgene panelmolecular targeted therapynext-generation sequencingnon-small cell lung carcinoma

Identifiers

PMID37189577
PMCPMC10137435
OpenAlexW4366548462

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.