The American Journal of Surgical Pathology · 2020 · 86 citations · 39 references
A novel finding in our study was the discovery of a VIM-RET fusion in 1 patient with SC of the parotid gland who could possibly benefit from RET-targeted therapy. In addition, 1 recurrent high-grade case was shown to harbor 2 different fusions, namely, ETV6-NTRK3 and MYB-SMR3B. The expanded molecular spectrum provides a novel insight into SC oncogenesis and carries important implications for molecular diagnostics, as this is the first SC-associated translocation with a non-ETV6 5' fusion partner. This finding further expands the definition of SC while carrying implications for selecting the appropriate targeted therapy.
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Alena Skálová, Tomáš Vaněček, Radek Šíma et al. · The American Journal of Surgical Pathology · 2010 · 995 citations
A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma
Stevan R. Knezevich, Deborah E. McFadden, Tao Wen et al. · Nature Genetics · 1998 · 796 citations
Congenital Fibrosarcoma, Pathology, Disease Gene Identification +4