Abstract | INTRODUCTION: AREAS COVERED:
Trabectedin has multiple mechanisms of action, including one targeting the FUS-CHOP oncogene in Myxoid/ Round cell Liposarcomas. Numerous Phase I, II and III clinical trials have been conducted with Trabectedin. It has been studied as monotherapy or in combination with other chemotherapeutic agents. The recommended dose based on clinical trials is 1.5 milligrams/m(2) continuous infusion over 24 hours once every 3 weeks for STS with evidence of disease control in multiple clinical trials at this dose. The most common Grade 3/4 toxicities include neutropenia and transient noncumulative elevations of ALT and AST. Steroid pretreatment has shown efficacy in reducing liver and bone marrow toxicity. In phase III testing comparing trabectedin to dacarbazine, trabectedin was associated with a significantly improved progression free survival rate in patients with advanced lipo- and leiomyosarcomas. EXPERT OPINION:
Trabectedin is an important new addition to the limited treatment options currently available for STS, especially for patients with liposarcoma that have progressed on standard chemotherapeutic regimens.
|
Authors | Ritika Zijoo, Margaret von Mehren |
Journal | Expert opinion on pharmacotherapy
(Expert Opin Pharmacother)
Vol. 17
Issue 14
Pg. 1953-62
(Oct 2016)
ISSN: 1744-7666 [Electronic] England |
PMID | 27615729
(Publication Type: Journal Article, Review)
|
Chemical References |
- Antineoplastic Agents, Alkylating
- Dioxoles
- Tetrahydroisoquinolines
- Trabectedin
|
Topics |
- Antineoplastic Agents, Alkylating
(pharmacology, therapeutic use)
- Dioxoles
(therapeutic use)
- Disease-Free Survival
- Female
- Humans
- Leiomyosarcoma
(drug therapy)
- Liposarcoma
(drug therapy)
- Sarcoma
(drug therapy)
- Tetrahydroisoquinolines
(therapeutic use)
- Trabectedin
|