Medicine Department, Institut de Cancérologie Gustave Roussy, 114 Rue Edouard Vaillant, 94805 Villejuif, France.
Expert Rev Anticancer Ther. 2013 Jun;13(6 Suppl 1):11-9. doi: 10.1586/era.13.49.
Trabectedin (Yondelis(®) [PharmaMar S.A., Madrid, Spain]) is one of the most promising agents tested in the last two decades in patients with anthracycline/ifosfamide-resistant sarcomas and is the first agent highlighting the notion of prolonged tumor control in advanced soft tissue sarcoma. Indeed, the unusual pattern of tumor response to trabectedin has raised queries about the appropriateness of conventional radiological evaluation of efficacy according to Response Evaluation Criteria in Solid Tumors and has prompted the search for new end points for Phase II studies. The safety profile of trabectedin is unique and much more favorable than that of doxorubicin and ifosfamide especially as regards neutropenia and alopecia. Its efficacy in translocation-related sarcomas suggests a targeted approach to tumor control in these sarcoma subtypes. With numerous Phase II and III studies of trabectedin underway, it appears certain that the current standard-of-care paradigm in advanced soft tissue sarcoma is set for change.
曲贝替定(Yondelis®)[西班牙马德里 PharmaMar S.A. 公司]是过去二十年中在蒽环类/异环磷酰胺耐药肉瘤患者中测试的最有前途的药物之一,是第一个强调晚期软组织肉瘤中延长肿瘤控制概念的药物。事实上,曲贝替定对肿瘤的异常反应模式引发了关于根据实体瘤反应评估标准(RECIST)进行疗效常规影像学评估的适宜性的疑问,并促使寻找新的 II 期研究终点。曲贝替定的安全性特征是独特的,并且比多柔比星和异环磷酰胺好得多,特别是在中性粒细胞减少和脱发方面。其在易位相关性肉瘤中的疗效表明针对这些肉瘤亚型的肿瘤控制的靶向方法。随着曲贝替定的多项 II 期和 III 期研究的进行,目前在晚期软组织肉瘤中的标准治疗模式似乎肯定会发生改变。