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多柔比星脂质体注射液治疗晚期软组织肉瘤的优化使用

Trabectedin for advanced soft tissue sarcomas: optimizing use.

机构信息

Sarcoma Unit, The Royal Marsden NHS Foundation Trust, London, UK.

出版信息

Ther Clin Risk Manag. 2014 Dec 12;10:1003-11. doi: 10.2147/TCRM.S49330. eCollection 2014.

Abstract

Patients with locally advanced or metastatic soft tissue sarcoma have a poor outlook with median survival in the order of 1 year. There is therefore an urgent need for novel agents to impact this disease. Trabectedin is one such novel agent that has demonstrated activity for patients with advanced soft tissue sarcoma and it was licensed in Europe in 2007 for patients in the second-line setting or first-line in those patients deemed unsuitable to receive cytotoxics. In order to best serve patients with novel agents, it is imperative to understand the mechanism or mechanisms of action and the best ways of assessing response in order to optimize antitumor activity. Frequently, the mechanism of action and the optimal means of assessing response will be different from those of traditional cytotoxics. Trial design should reflect these factors to ensure that active drugs are not wrongly marked as futile. This review discusses a number of factors that may influence the optimization of trabectedin use. These factors include the administration schedule, the optimal timing of trabectedin administration in the disease process, the histopathological and molecular subtypes that may be most sensitive to trabectedin, the challenge of assessing response, particularly using radiology, and, finally, the safety considerations with this agent.

摘要

局部晚期或转移性软组织肉瘤患者预后较差,中位生存期约为 1 年。因此,迫切需要新型药物来治疗这种疾病。 trabectedin 是一种新型药物,已被证明对晚期软组织肉瘤患者有效,并于 2007 年在欧洲获得许可,适用于二线治疗或不适合接受细胞毒药物治疗的一线治疗患者。为了使患者最好地受益于新型药物,必须了解其作用机制和最佳反应评估方法,以优化抗肿瘤活性。通常,作用机制和最佳反应评估方法与传统细胞毒药物不同。试验设计应反映这些因素,以确保不会错误地将活性药物标记为无效。本文讨论了一些可能影响 trabectedin 应用优化的因素。这些因素包括给药方案、疾病过程中 trabectedin 给药的最佳时机、可能对 trabectedin 最敏感的组织病理学和分子亚型、评估反应的挑战,特别是使用影像学,以及最后,该药物的安全性考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb9/4270297/8c9d6d11346b/tcrm-10-1003Fig1.jpg

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