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充分利用现有选择,实现肉瘤治疗的最优化。

Making the Best of Available Options for Optimal Sarcoma Treatment.

机构信息

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

出版信息

Oncology. 2018;95 Suppl 1:11-20. doi: 10.1159/000494861. Epub 2018 Dec 14.

Abstract

For 35 years options for treating advanced soft tissue sarcoma (STS) were limited to doxorubicin, dacarbazine and ifosfamide. In 2007, trabectedin was approved. Since then, several other agents have become available and many more are in development, ushering in a new era in disease management. Considerable scope exists for improving outcomes of advanced STS through better trial design and improved patient care in everyday practice. After anthracycline failure, there are a range of treatment options and, increasingly, the choice of therapy is histology driven. Introduction of newer agents and optimising use of established agents such as trabectedin has led to an increase in overall survival of advanced STS patients. Optimising treatment with trabectedin is being achieved through more extensive experience in drug management, mainly associated with use in earlier lines and uninterrupted use until disease progression. Identification by next-generation sequencing of a significant proportion of cases of actionable mutations among patients with advanced STS suggests a move towards matched therapy in future. As the armamentarium of active agents in advanced sarcoma increases, so too will the challenge of selecting the right drug for the right patient at the right time, in accordance with the patient's lifestyle and wishes.

摘要

35 年来,治疗晚期软组织肉瘤(STS)的选择有限,仅限于多柔比星、达卡巴嗪和异环磷酰胺。2007 年,曲贝替定获批。此后,又出现了几种其他药物,还有更多药物正在开发中,这为疾病管理带来了一个新时代。通过更好的试验设计和提高日常实践中的患者护理,在改善晚期 STS 的结果方面有很大的空间。在蒽环类药物失败后,有一系列的治疗选择,并且越来越多的治疗选择是基于组织学驱动的。新型药物的引入以及对多柔比星等已确立药物的优化使用,导致晚期 STS 患者的总体生存率提高。通过在药物管理方面积累更广泛的经验,主要是在早期治疗线中使用和疾病进展前不间断使用,实现了曲贝替定治疗的优化。通过下一代测序在晚期 STS 患者中鉴定出大量可操作突变的比例,这表明未来将朝着针对特定突变的靶向治疗方向发展。随着晚期肉瘤中有效药物的不断增加,如何根据患者的生活方式和意愿,在正确的时间为正确的患者选择正确的药物,也将成为一个挑战。

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