Malignant Epithelioid Hemangioendothelioma of the Liver Successfully Treated with Sorafenib
Author(s) -
Bruno Sangro,
Mercedes Iñarrairaegui,
Nerea Fernández-Ros
Publication year - 2012
Publication title -
rare tumors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.285
H-Index - 15
eISSN - 2036-3613
pISSN - 2036-3605
DOI - 10.4081/rt.2012.e34
Subject(s) - medicine , sorafenib , epithelioid hemangioendothelioma , bevacizumab , regorafenib , vascular endothelial growth factor , hepatocellular carcinoma , hemangioendothelioma , thalidomide , calcification , pathology , oncology , gastroenterology , vegf receptors , immunohistochemistry , colorectal cancer , cancer , chemotherapy , multiple myeloma
Epithelioid hemangioendothelioma (HEH) is a rare disease of unknown etiology for which a standard systemic treatment has not been established. The common expression of vascular endothelial growth factor (VEGF) and its receptor in HEH provide a rationale for the reported use of antiangiogenic drugs, including bevacizumab, lenalidomide and thalidomide. We report a case of a young male patient with HEH with sorafenib for almost 2 years. Sorafenib was used instead of other VEGF inhibitors due to its convenient oral route, its dual antiangiogenic and antiproliferative activity, and its favorable safety profile. Sorafenib therapy resulted in durable stabilization with progressive calcification of liver tumors and minor but stable response of lung lesions
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