| Literature DB >> 32915420 |
Weifeng Liu1,2, Qianqian Duan3, Lihua Gong4, Yongkun Yang1, Zhen Huang1, Hao Guo3, Xiaohui Niu5.
Abstract
An inflammatory myofibroblastic tumor (IMT) is a rare invasive soft tissue mass with intramuscular penetration that is primarily treated via a surgical procedure. However, with unclear boundaries and a high rate of relapse, there is no standard treatment for recurrence or unresectable tumors. It is noteworthy that approximately half of IMTs harbor genetic rearrangements of the anaplastic lymphoma kinase (ALK). ALK inhibitors have been used successfully in the treatment of IMTs with a variety of ALK fusions. Here, we present a case of a 15-year-old patient with IMT around the hip. Next-generation sequencing (NGS) revealed an LRRFIP1-ALK fusion, which has not yet been reported in the literature. Crizotinib, an ALK inhibitor, was effective in the treatment of this patient, indicating that ALK inhibitors may be effective for IMT with LRRFIP1-ALK fusions. This report expands the list of gene fusions in IMTs and highlights a new target for treatment.Entities:
Keywords: Crizotinib; Inflammatory myofibroblastic tumor; LRRFIP1-ALK fusion; Novel target
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Year: 2020 PMID: 32915420 DOI: 10.1007/s10637-020-00984-5
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850