Evidence map›Paper›PMID 32022484›Full record

ArticleThe journal of pathology. Clinical research2020

NTRK fusions in osteosarcoma are rare and non-functional events.

Baptiste Ameline, Karim H Saba, Michal Kovac, Linda Magnusson, Olaf Witt, Stefan Bielack, Michaela Nathrath, Karolin H Nord, Daniel Baumhoer

Open access · goldAbstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 11% 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, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Future oncology (London, England) · 2025
    Pooled it
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  3. JCO precision oncology · 2026
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  15. Diagnostics (Basel, Switzerland) · 2021
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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

9 authors at 5 institutions in 3 countries.

Baptiste AmelineBone Tumour Reference Center at the Institute of Pathology, University and University Hospital Basel, Basel, Switzerland.ORCID 0000-0001-5913-7413
Karim H SabaDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Michal KovacBone Tumour Reference Center at the Institute of Pathology, University and University Hospital Basel, Basel, Switzerland.
Linda MagnussonDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.
Olaf WittCoordinator INFORM Program, Hopp Children's Cancer Center, German Cancer Research Center, University Hospital Heidelberg, Heidelberg, Germany.
Stefan BielackCooperative Osteosarcoma Study Group, Stuttgart Cancer Center, Klinikum Stuttgart - Olgahospital, Pediatrics 5 (Oncology, Hematology, Immunology), Stuttgart, Germany.
Michaela NathrathDepartment of Pediatrics, Pediatric Oncology Center, Technische Universität München, Munich, Germany.
Karolin H NordDepartment of Laboratory Medicine, Division of Clinical Genetics, Lund University, Lund, Sweden.ORCID 0000-0002-2397-2254
Daniel BaumhoerBone Tumour Reference Center at the Institute of Pathology, University and University Hospital Basel, Basel, Switzerland.
Lund University · SEUniversity Hospital of Basel · CHGerman Cancer Research Center · DEKlinikum Kassel · DEOlgahospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotrophic tyrosine receptor kinase (NTRK) fusions are promising molecular targets that have been described in a broad range of malignant tumours. Fusions commonly lead to the expression of chimeric proteins with constitutive tyrosine kinase activation that drives tumorigenesis. Despite a low prevalence among most solid tumours (<1%), the first encouraging results with pan-NTRK tyrosine kinase inhibitors (TKIs) such as larotrectinib or entrectinib stimulated the search for eligible patients. Here, we report the first three cases of osteosarcoma harbouring NTRK fusions, among 113 patients sequenced. It is also the first report on NTRK fusions within a tumour type characterised by highly rearranged genomes and abundant passenger mutations. Whereas the presence of NTRK gene fusions in many tumours is considered to be one of the main driver events for tumour progression, the three chimeric transcripts described here appear non-functional and likely represent randomly occurring passenger alterations. Particularly in tumours with complex karyotypes, it may therefore be advisable to specifically investigate the fusion transcripts for functional impact before considering targeted treatment approaches using pan-NTRK TKIs.

Indexed as

Bone NeoplasmsCell Transformation, NeoplasticHumansOncogene Proteins, FusionOsteosarcomaProtein Kinase InhibitorsReceptor, trkAReceptor, trkCNTRK1 protein, humanOncogene Proteins, FusionProtein Kinase InhibitorsReceptor, trkAReceptor, trkCNTRKosteosarcomatyrosine kinase inhibitors

Identifiers

PMID32022484
PMCPMC7164374
OpenAlexW3004913724

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.