Evidence map›Paper›PMID 34310819›Full record

ArticleCancer science2021

Highly sensitive fusion detection using plasma cell-free RNA in non-small-cell lung cancers.

Nobuhiko Hasegawa, Shinji Kohsaka, Kana Kurokawa, Yuki Shinno, Ikuko Takeda Nakamura, Toshihide Ueno, Shinya Kojima, Masahito Kawazu, Yoshiyuki Suehara, Muneaki Ishijima and 9 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-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

36 citing papers in PubMed, 47 citations in OpenAlex.

  1. Serial Cell-Free DNA Sequencing inJCO precision oncology · 2024
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  17. [A Case of EML4-ALK Fusion V1 Subtype Lung Adenocarcinoma 
Detected by RNA-based NGS].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2024
    Article
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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

19 authors at 1 institution in 1 country.

Nobuhiko HasegawaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Shinji KohsakaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8651-6136
Kana KurokawaDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yuki ShinnoDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Ikuko Takeda NakamuraDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Toshihide UenoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Shinya KojimaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Masahito KawazuDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Yoshiyuki SueharaDepartment of Medicine for Orthopaedics and Motor Organ, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Muneaki IshijimaDepartment of Medicine for Orthopaedics and Motor Organ, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yasushi GotoDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yuki KojimaDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Kan YonemoriDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7624-7611
Takuo HayashiDepartment of Human Pathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Tsuyoshi SaitoDepartment of Human Pathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9690-8440
Takehito ShukuyaDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Fumiyuki TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hiroyuki ManoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4645-0181
Juntendo University · JP

Funding

Japan Agency for Medical Research and Development JP20ck0106536Japan Agency for Medical Research and Development JP20cm0106502National Cancer Center Research and Development Fund 31-A-1
6 · The paper itself

Abstract

ALK, ROS1, and RET kinase fusions are important predictive biomarkers of tyrosine kinase inhibitors (TKIs) in non-small-cell lung cancer (NSCLC). Analysis of cell-free DNA (cfDNA) provides a noninvasive method to identify gene changes in tumor cells. The present study sought to use cfRNA and cfDNA for identifying fusion genes. A reliable protocol was established to detect fusion genes using cfRNA and assessed the analytical validity and clinical usefulness in 30 samples from 20 cases of fusion-positive NSCLC. The results of cfRNA-based assays were compared with tissue biopsy and cfDNA-based liquid biopsy (Guardant360 plasma next-generation sequencing [NGS] assay). The overall sensitivity of the cfRNA-based assay was 26.7% (8/30) and that of cfDNA-based assay was 16.7% (3/18). When analysis was limited to the samples collected at chemo-naïve or progressive disease status and available for both assays, the sensitivity of the cfRNA-based assay was 77.8% (7/9) and that of cfDNA-based assay was 33.3% (3/9). Fusion gene identification in cfRNA was correlated with treatment response. These results suggest that the proposed cfRNA assay is a useful diagnostic test for patients with insufficient tissues to facilitate effective administration of first-line treatment and is a useful tool to monitor the progression of NSCLC for consideration of second-line treatments.

Indexed as

Cell-Free Nucleic AcidsGene FusionAdultAgedAged, 80 and overAnaplastic Lymphoma KinaseBiomarkers, TumorBiopsyCarbazolesCarcinoma, Non-Small-Cell LungCrizotinibCytoskeletal ProteinsDisease ProgressionDrug Resistance, NeoplasmEzrinFemalealectinibAnaplastic Lymphoma KinaseBiomarkers, TumorCarbazolesCell-Free Nucleic AcidsCrizotinibCytoskeletal ProteinsEML4-ALK fusion protein, humanEzrinGAPDH protein, humanGlyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)KIF5B-ALK fusion protein, humanOncogene Proteins, FusionPiperidinesProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-retRET protein, humanRNA, MessengerROS1 protein, humancell-free DNAcell-free RNAfusion geneliquid biopsynon-small-cell lung cancer

Identifiers

PMID34310819
PMCPMC8486187
OpenAlexW3183262704

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.