Evidence map›Paper›PMID 37545217›Full record

ArticleCancer biomarkers : section A of Disease markers2023

Pan-TRK immunohistochemistry as screening tool for NTRK fusions: A diagnostic workflow for the identification of positive patients in clinical practice.

Andrea Vingiani, Daniele Lorenzini, Elena Conca, Chiara Costanza Volpi, Desirè Viola Trupia, Annunziata Gloghini, Federica Perrone, Elena Tamborini, Gian Paolo Dagrada, Luca Agnelli and 3 more

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Article in Cancer biomarkers : section A of Disease markers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Cost-Efficient Detection ofInternational journal of molecular sciences · 2023
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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

13 authors at 1 institution in 1 country.

Andrea VingianiDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Daniele LorenziniDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Elena ConcaDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Chiara Costanza VolpiDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Desirè Viola TrupiaDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Annunziata GloghiniDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Federica PerroneDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Elena TamboriniDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Gian Paolo DagradaDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Luca AgnelliDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Iolanda CaponeDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Adele BusicoDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
Giancarlo PruneriDepartment of Diagnostic Innovation, Foundation IRCCS National Cancer Institute, Milan, Italy.
University of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPan-TRK inhibitors Entrectinib and Larotrectinib have been recently approved as tumor-agnostic therapies in NTRK1-2-3 rearranged patients and there is therefore an urgent need to identify reliable and accessible biomarkers for capturing NTRK fusions in the real-world practice.

objectiveWe aim to assess the analytical validity of the recently released pan-TRK assay (Ventana), running a head-to-head comparison between immunohistochemistry and Archer FusionPlex Lung Panel (ArcherDX) that is designed to detect key fusions in 13 genes, also including NTRK1-3.

methodsPan-TRK IHC and NGS analysis were conducted on a retrospective/prospective cohort of 124 cancer patients (carcinomas, 93 cases; soft tissue sarcomas, 19; primary central nervous system tumours, 10; and neuroblastomas, 2). FISH data were available in most of the IHC/NGS discordant cases.

resultsA comparison between IHC and NGS results was carried out in 117 cases: among 30 pan-TRK positive cases, NTRK rearrangement by NGS was found in 11 (37%), while one of the 87 (1.1%) pan-TRK negative cases (a case of NSCLC) showed a TPM3-NRTK1 rearrangement by NGS. Accordingly, sensitivity and specificity of IHC in predicting NTRK status were 91.7% and 81.9%, respectively, while negative (NPV) and positive predictive value (PPV) were 98.8% and 36.7%, respectively.

conclusionsThese data lead to suggest that IHC with VENTANA pan-TRK antibody can be a reliable screening tool for the identification of patients potentially bearing NTRK rearranged tumours.

Indexed as

Lung NeoplasmsHumansImmunohistochemistryProspective StudiesRetrospective StudiesWorkflowBiomarkerFluorescent in Situ Ibridizationimmunohistochemistrynext-generation sequencingNTRK

Identifiers

PMID37545217
PMCPMC12412862
OpenAlexW4385576951

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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.