Unité de Jour d'Oncologie Médicale Multidisciplinaire, Hôpital Edouard Herriot Lyon, France.
Ther Clin Risk Manag. 2008 Feb;4(1):109-16. doi: 10.2147/tcrm.s1174.
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 mug/m(2) 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.
曲贝替定是一种新型的海洋来源的化合物,可与 DNA 小沟结合,并与 DNA 修复机制的蛋白相互作用。I 期临床试验确立了标准方案为 1500μg/m(2),24 小时持续输注,每 3 周重复一次。几项 II 期临床试验显示,在未经选择的软组织肉瘤患者中,有 5%-10%的患者对先前的化疗有反应,且疾病稳定率为 30%-40%。此外,在 15%-20%的患者中描述了延长的疾病控制。毒性主要为血液学和肝脏毒性,约有 50%和 20%的患者分别观察到 3-4 级中性粒细胞减少症和血小板减少症,有 35%-50%的接受曲贝替定治疗的患者观察到 3-4 级肝酶升高。目前的研究重点是确定接受曲贝替定治疗的软组织肉瘤患者的预测因素。