Role of trabectedin in the treatment of soft tissue sarcoma

Autor: Alexandre Christinat, Serge Leyvraz
Jazyk: angličtina
Rok vydání: 2009
Předmět:
Oncology
medicine.medical_specialty
Pathology
medicine.medical_treatment
Review
Ecteinascidia turbinata
chemotherapy
lcsh:RC254-282
Internal medicine
Medicine
Pharmacology (medical)
Trabectedin
Dexamethasone
Chemotherapy
medicine.diagnostic_test
biology
business.industry
Soft tissue sarcoma
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
biology.organism_classification
Cell culture
soft tissue sarcoma
trabectedin
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols/administration & dosage
Chromosomes
Human
Pair 14

Chromosomes
Human
Pair 4

Cytarabine/administration & dosage
Dexamethasone/administration & dosage
Disease-Free Survival
Female
Follow-Up Studies
Genetic Heterogeneity
Hemoglobins
Humans
Male
Middle Aged
Multiple Myeloma/drug therapy
Multiple Myeloma/genetics
Multivariate Analysis
Prognosis
Retrospective Studies
Translocation
Genetic

Vincristine/administration & dosage
beta 2-Microglobulin/blood
Premedication
business
Liver function tests
DNA-minor groove binder
medicine.drug
Zdroj: OncoTargets and therapy
Oncotargets and Therapy, vol. 2, no. 9, pp. 105-113
OncoTargets and Therapy, Vol 2009, Iss default, Pp 105-113 (2009)
ISSN: 1178-6930
Popis: Alexandre Christinat, Serge LeyvrazCentre Pluridisciplinaire d’Oncologie, University Hospital, Lausanne, SwitzerlandAbstract: Interest in marine natural products has allowed the discovery of new drugs and trabectedin (ET-743, Yondelis), derived from the marine tunicate Ecteinascidia turbinata, was approved for clinical use in 2007. It binds to the DNA minor groove leading to interferences with the intracellular transcription pathways and DNA-repair proteins. In vitro antitumor activity was demonstrated against various cancer cell lines and soft tissue sarcoma cell lines. In phase I studies tumor responses were observed also in osteosarcomas and different soft tissue sarcoma subtypes. The most common toxicities were myelosuppression and transient elevation of liver function tests, which could be reduced by dexamethasone premedication. The efficacyof trabectedin was established in three phase II studies where it was administered at 1.5 mg/m2 as a 24 h intravenous infusion repeated every three weeks, in previously treated patients. The objective response rate was 3.7%–8.3% and the tumor control rate (which included complete response, partial response and stable disease) was obtained in half of patients for a median overall survival reaching 12 months. In nonpretreated patients the overall response rate was 17%. Twenty-four percent of patients were without progression at six months. The median overall survival was almost 16 months with 72% surviving at one year. Predictive factors of response are being explored to identify patients who are most likely to respond to trabectedin. Combination with other agents are currently studied with promising results. In summary trabectedin is an active new chemotherapeutic agents that has demonstrated its role in the armamentarium of treatments for patients with sarcomas.Keywords: soft tissue sarcoma, trabectedin, chemotherapy, DNA-minor groove binder
Databáze: OpenAIRE