User: Guest  Login
Title:

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

Document type:
Article; Journal Article; Research Support, Non-U.S. Gov't
Author(s):
Ameline, Baptiste; Saba, Karim H; Kovac, Michal; Magnusson, Linda; Witt, Olaf; Bielack, Stefan; Nathrath, Michaela; Nord, Karolin H; Baumhoer, Daniel
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.
Journal title abbreviation:
J Pathol Clin Res
Year:
2020
Journal volume:
6
Journal issue:
2
Pages contribution:
107-112
Fulltext / DOI:
doi:10.1002/cjp2.158
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/32022484
TUM Institution:
Klinik und Poliklinik für Kinderheilkunde und Jugendmedizin
 BibTeX