Abstract |
Liposarcoma is one of the most common adult soft tissue sarcomas and consists of three histologic subtypes (well and dedifferentiated, myxoid/round cell, and pleomorphic). Surgery is the mainstay of treatment for localized disease; however for unresectable or metastatic disease, effective treatment options are currently limited. In the past decade, a better understanding of the distinct genetic and molecular aberrations for each of the three histologic subtypes has led to the development of several novel systemic therapies. Data from phase I and early phase II clinical trials have been reported. Despite challenges with conducting clinical trials in liposarcoma, preliminary results for several of these novel, biology-driven therapies are encouraging.
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Authors | William W Tseng, Neeta Somaiah, Alexander J Lazar, Dina C Lev, Raphael E Pollock |
Journal | Cancers
(Cancers (Basel))
Vol. 5
Issue 2
Pg. 529-49
(May 10 2013)
ISSN: 2072-6694 [Print] Switzerland |
PMID | 24216990
(Publication Type: Journal Article)
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