| Literature DB >> 28351781 |
Andrés Poveda1, Xavier García Del Muro2, Jose Antonio López-Guerrero3, Ricardo Cubedo4, Virginia Martínez5, Ignacio Romero6, César Serrano7, Claudia Valverde7, Javier Martín-Broto8.
Abstract
Gastrointestinal stromal sarcomas (GISTs) are the most common mesenchymal tumours originating in the digestive tract. They have a characteristic morphology, are generally positive for CD117 (c-kit) and are primarily caused by activating mutations in the KIT or PDGFRA genes(1). On rare occasions, they occur in extravisceral locations such as the omentum, mesentery, pelvis and retroperitoneum. GISTs have become a model of multidisciplinary work in oncology: the participation of several specialties (oncologists, pathologists, surgeons, molecular biologists, radiologists…) has forested advances in the understanding of this tumour and the consolidation of a targeted therapy, imatinib, as the first effective molecular treatment in solid tumours. Following its introduction, median survival of patients with advanced or metastatic GIST increased from 18 to more than 60months. Sunitinib and Regorafenib are two targeted agents with worldwide approval for second- and third-line treatment, respectively, in metastatic GIST.Entities:
Keywords: CD117; DOG1; GEIS; GIST; Imatinib; KIT; PDGFRA; Regorafenib; Sunitinib
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Year: 2017 PMID: 28351781 DOI: 10.1016/j.ctrv.2016.11.011
Source DB: PubMed Journal: Cancer Treat Rev ISSN: 0305-7372 Impact factor: 12.111