| Literature DB >> 34244015 |
Priya Mahajan1, Michela Casanova2, Andrea Ferrari2, Ashleigh Fordham3, Toby Trahair4, Rajkumar Venkatramani5.
Abstract
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumor of intermediate malignant potential that predominantly affects children, adolescents and young adults. IMT has a predilection for the lung, abdomen, pelvis, and retroperitoneum, however, can affect any part of the body. IMT is typically localized, and multifocal or metastatic disease is uncommon. Complete surgical resection is the treatment of choice when feasible. There is no established standard of care for unresectable and advanced IMT. Approximately half of IMTs harbor anaplastic lymphoma kinase (ALK) gene rearrangements, and fusions involving ROS1, PDGFRβ, RET and NTRK have also been described. Given the molecular landscape of IMT, management of these tumors has evolved to include tyrosine kinase inhibitors and novel targeted therapeutics. This review highlights the molecular characteristics, evolution of targeted therapies and the remaining challenges in the management of IMT.Entities:
Keywords: Inflammatory myofibroblastic tumor; molecular profiling; pediatrics; rare tumor; targeted therapy, crizotinib, ALK inhibition
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Year: 2021 PMID: 34244015 DOI: 10.1016/j.currproblcancer.2021.100768
Source DB: PubMed Journal: Curr Probl Cancer ISSN: 0147-0272 Impact factor: 3.187