@ARTICLE{10.3389/pore.2022.1610423, AUTHOR={Siozopoulou, Vasiliki and Marcq, Elly and De Winne, Koen and Norga, Koen and Schmitz, Gertjan and Duwel, Valerie and Delvenne, Philippe and Smits, Evelien and Pauwels, Patrick}, TITLE={NTRK Fusions in a Sarcomas Series: Pathology, Molecular and Clinical Aspects}, JOURNAL={Pathology and Oncology Research}, VOLUME={28}, YEAR={2022}, URL={https://www.por-journal.com/articles/10.3389/pore.2022.1610423}, DOI={10.3389/pore.2022.1610423}, ISSN={1532-2807}, ABSTRACT={Targeting molecular alterations has been proven to be an inflecting point in tumor treatment. Especially in recent years, inhibitors that target the tyrosine receptor kinase show excellent response rates and durable effects in all kind of tumors that harbor fusions of one of the three neurotrophic tyrosine receptor kinase genes (NTRK1, NTRK2 and NTRK3). Today, the therapeutic options in most metastatic sarcomas are rather limited. Therefore, identifying which sarcoma types are more likely to harbor these targetable NTRK fusions is of paramount importance. At the moment, identification of these fusions is solely based on immunohistochemistry and confirmed by molecular techniques. However, a first attempt has been made to describe the histomorphology of NTRK-fusion positive sarcomas, in order to pinpoint which of these tumors are the best candidates for testing. In this study, we investigate the immunohistochemical expression of pan-TRK in 70 soft tissue and bone sarcomas. The pan-TRK positive cases were further investigated with molecular techniques for the presence of a NTRK fusion. Seven out of the 70 cases showed positivity for pan-TRK, whereas two of these seven cases presented an NTRK3 fusion. Further analysis of the fused sarcomas revealed some unique histological, molecular and clinical findings. The goal of this study is to expand the histomorphological spectrum of the NTRK-fused sarcomas, to identify their fusion partners and to correlate these parameters with the clinical outcome of the disease. In addition, we evaluated the immunohistochemical expression pattern of the pan-TRK and its correlation with the involved NTRK gene.} }