| Literature DB >> 18445656 |
David Hong1, Lei Ye, Robert Gagel, Lakshmi Chintala, Adel K El Naggar, John Wright, Razelle Kurzrock.
Abstract
Medullary thyroid carcinoma (MTC) is an uncommon malignancy of hereditary and sporadic presentation. Mutations in the RET proto-oncogene are involved in the pathogenesis of familial MTC and >50% of the sporadic cases. Currently, there is no effective treatment for recurrent or metastatic MTC. We report here a rapid response to a sorafenib (RET and RAF kinase and vascular endothelial growth factor receptor inhibitor)--based regimen in a patient with sporadic MTC who had advanced, progressive disease and a novel RET kinase aberration at exon 11 shown in tumor tissue.Entities:
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Year: 2008 PMID: 18445656 DOI: 10.1158/1535-7163.MCT-07-2422
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261