Trabectedin and its potential in the treatment of soft tissue sarcoma

Philippe A Cassier1, Armelle Dufresne1, Jean-Yves Blay1,2,3, Jérôme Fayette2,31Unité de Jour d’Oncologie Médicale Multidisciplinaire, Hôpital Edouard Herriot, Lyon, France; 2Département d&rs...

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Main Authors: Philippe A Cassier, Armelle Dufresne, Jean-Yves Blay, Jérôme Fayette
Format: Article
Language:English
Published: Dove Medical Press 2008-03-01
Series:Therapeutics and Clinical Risk Management
Online Access:http://www.dovepress.com/trabectedin-and-its-potential-in-the-treatment-of-soft-tissue-sarcoma-a1290
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spelling doaj-7765f5567f9a41e6b4d227e91ca6a1442020-11-24T23:47:00ZengDove Medical PressTherapeutics and Clinical Risk Management1176-63361178-203X2008-03-012008Issue 1109116Trabectedin and its potential in the treatment of soft tissue sarcomaPhilippe A CassierArmelle DufresneJean-Yves BlayJérôme FayettePhilippe A Cassier1, Armelle Dufresne1, Jean-Yves Blay1,2,3, Jérôme Fayette2,31Unité de Jour d’Oncologie Médicale Multidisciplinaire, Hôpital Edouard Herriot, Lyon, France; 2Département d’Oncologie Médicale, Centre Léon Bérard, Lyon, France; 3Unité INSERM 590, Equipe Cytokine et Cancer, Centre Léon Bérard, Lyon, FranceAbstract: Trabectedin is a new marine-derived compound that binds the DNA minor groove and interacts with proteins of the DNA repair machinery. Phase I trials have established the standard regimen as 1500 µg/m² 24-hour continuous infusion repeated every 3 weeks. Several phase II trials have shown response in 5%–10% of unselected patients with soft tissue sarcoma failing prior chemotherapy and disease stabilisation in 30%–40%. Furthermore, prolonged disease control has been described in 15%–20% of patients. Toxicities are mainly haematological and hepatic with grade 3–4 neutropenia and thrombocytopenia observed in approximately 50% and 20% of patients respectively, and grade 3–4 elevation of liver enzymes observed in 35%–50% of patients treated with trabectedin. Current research focuses on the identification of predictive factors for patients with soft tissue sarcoma treated with trabectedin.Keywords: chemotherapy, sarcoma, drug development, DNA repair http://www.dovepress.com/trabectedin-and-its-potential-in-the-treatment-of-soft-tissue-sarcoma-a1290
collection DOAJ
language English
format Article
sources DOAJ
author Philippe A Cassier
Armelle Dufresne
Jean-Yves Blay
Jérôme Fayette
spellingShingle Philippe A Cassier
Armelle Dufresne
Jean-Yves Blay
Jérôme Fayette
Trabectedin and its potential in the treatment of soft tissue sarcoma
Therapeutics and Clinical Risk Management
author_facet Philippe A Cassier
Armelle Dufresne
Jean-Yves Blay
Jérôme Fayette
author_sort Philippe A Cassier
title Trabectedin and its potential in the treatment of soft tissue sarcoma
title_short Trabectedin and its potential in the treatment of soft tissue sarcoma
title_full Trabectedin and its potential in the treatment of soft tissue sarcoma
title_fullStr Trabectedin and its potential in the treatment of soft tissue sarcoma
title_full_unstemmed Trabectedin and its potential in the treatment of soft tissue sarcoma
title_sort trabectedin and its potential in the treatment of soft tissue sarcoma
publisher Dove Medical Press
series Therapeutics and Clinical Risk Management
issn 1176-6336
1178-203X
publishDate 2008-03-01
description Philippe A Cassier1, Armelle Dufresne1, Jean-Yves Blay1,2,3, Jérôme Fayette2,31Unité de Jour d’Oncologie Médicale Multidisciplinaire, Hôpital Edouard Herriot, Lyon, France; 2Département d’Oncologie Médicale, Centre Léon Bérard, Lyon, France; 3Unité INSERM 590, Equipe Cytokine et Cancer, Centre Léon Bérard, Lyon, FranceAbstract: Trabectedin is a new marine-derived compound that binds the DNA minor groove and interacts with proteins of the DNA repair machinery. Phase I trials have established the standard regimen as 1500 µg/m² 24-hour continuous infusion repeated every 3 weeks. Several phase II trials have shown response in 5%–10% of unselected patients with soft tissue sarcoma failing prior chemotherapy and disease stabilisation in 30%–40%. Furthermore, prolonged disease control has been described in 15%–20% of patients. Toxicities are mainly haematological and hepatic with grade 3–4 neutropenia and thrombocytopenia observed in approximately 50% and 20% of patients respectively, and grade 3–4 elevation of liver enzymes observed in 35%–50% of patients treated with trabectedin. Current research focuses on the identification of predictive factors for patients with soft tissue sarcoma treated with trabectedin.Keywords: chemotherapy, sarcoma, drug development, DNA repair
url http://www.dovepress.com/trabectedin-and-its-potential-in-the-treatment-of-soft-tissue-sarcoma-a1290
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