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CPX-351在急性髓系白血病治疗格局中的作用:作用机制、疗效与安全性

The Role of CPX-351 in the Acute Myeloid Leukemia Treatment Landscape: Mechanism of Action, Efficacy, and Safety.

作者信息

Pagano Livio, Danesi Romano, Benedetti Edoardo, Morgagni Riccardo, Romani Luigina, Venditti Adriano

机构信息

Department of Laboratory and Hematological Sciences, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.

Department of Diagnostic Imaging, Radiotherapy Oncology, and Hematology, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Drugs. 2025 May 10. doi: 10.1007/s40265-025-02194-w.

Abstract

CPX-351 (also known as VYXEOS or Vyxeos liposomal) is a dual-drug liposomal encapsulation of cytarabine and daunorubicin in a synergistic 5:1 molar ratio and was the first example that utilized CombiPlex, a combination drug technology platform. Superior efficacy with CPX-351 in the pivotal phase 3 randomized clinical trial versus its conventional free-drug counterpart led to its approval for the treatment of newly diagnosed therapy-related acute myeloid leukemia (AML) or AML with myelodysplasia-related changes in multiple countries. Emerging evidence indicates that CPX-351 affords additional benefits compared with conventional chemotherapy, including protection against intestinal dysbiosis and fungal colonization, fewer infectious complications, and a lower incidence of cardiotoxicity. This review examines the mechanisms underlying CPX-351's therapeutic effects and highlights its expanding role in AML treatment by summarizing efficacy and safety data from preclinical models, the pivotal clinical trial, and real-world studies. Particular focus is given to recent findings on CPX-351's intestinal and cardioprotective properties, which together strengthen its safety and efficacy profile compared with conventional chemotherapy.

摘要

CPX-351(也称为VYXEOS或Vyxeos脂质体)是一种将阿糖胞苷和柔红霉素以5:1摩尔比协同封装在脂质体中的双药制剂,是首个利用联合药物技术平台CombiPlex的实例。在关键的3期随机临床试验中,CPX-351相对于其传统游离药物对应物具有更高的疗效,这使得它在多个国家被批准用于治疗新诊断的治疗相关急性髓系白血病(AML)或伴有骨髓发育异常相关改变的AML。新出现的证据表明,与传统化疗相比,CPX-351具有更多益处,包括预防肠道菌群失调和真菌感染、减少感染并发症以及降低心脏毒性发生率。本综述通过总结来自临床前模型、关键临床试验和真实世界研究的疗效和安全性数据,探讨了CPX-351治疗效果的潜在机制,并强调了其在AML治疗中不断扩大的作用。特别关注了CPX-351肠道和心脏保护特性的最新研究结果,与传统化疗相比,这些特性共同增强了其安全性和疗效。

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