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聚乙二醇化脂质体阿霉素相关的手足红斑感觉异常(“手足”综合征)

Pegylated liposomal doxorubicin-related palmar-plantar erythrodysesthesia ('hand-foot' syndrome).

作者信息

Lorusso D, Di Stefano A, Carone V, Fagotti A, Pisconti S, Scambia G

机构信息

Department of Oncology, Catholic University of the Sacred Heart, Campobasso, Italy.

出版信息

Ann Oncol. 2007 Jul;18(7):1159-64. doi: 10.1093/annonc/mdl477. Epub 2007 Jan 17.

DOI:10.1093/annonc/mdl477
PMID:17229768
Abstract

Palmar-plantar erythrodysesthesia (PPE), also called hand-foot syndrome or hand-to-foot syndrome, is a distinctive and relatively frequent dermatologic toxic reaction associated with certain chemotherapeutic agents. Pegylated liposomal doxorubicin (PLD), a long-circulating formulation of doxorubicin in which doxorubicin hydrochloride is encapsulated within pegylated liposomes, is approved to treat patients with metastatic breast cancer, advanced ovarian cancer, and acquired immunodeficiency syndrome-related Kaposi's sarcoma. The incidence of PPE is increased in patients receiving PLD compared with conventional doxorubicin. In studies that utilized the currently approved dose of PLD (50 mg/m(2) every 4 weeks), approximately 50% of all patients receiving PLD experienced PPE, and approximately 20% experienced grade 3 PPE. The pathophysiology of PPE, as it occurs with any drug with which it is associated, is not well understood. Studies evaluating the development of PPE specifically associated with PLD have not fully elucidated the mechanism; however, data support the roles of drug excretion in sweat and local pressure as contributors. When PPE develops, clinical interventions with respect to altering PLD administration include dose reduction, less frequent dosing, and ultimately, drug withdrawal with several consequences on treatment efficacy. This article will review the available data regarding the etiology and potential management strategies of PPE associated with PLD.

摘要

手足红斑性感觉异常(PPE),也称为手足综合征,是一种与某些化疗药物相关的独特且相对常见的皮肤毒性反应。聚乙二醇化脂质体阿霉素(PLD),一种阿霉素的长效循环制剂,其中盐酸阿霉素被包裹在聚乙二醇化脂质体中,被批准用于治疗转移性乳腺癌、晚期卵巢癌和获得性免疫缺陷综合征相关的卡波西肉瘤患者。与传统阿霉素相比,接受PLD治疗的患者中PPE的发生率有所增加。在使用当前批准剂量的PLD(每4周50 mg/m²)的研究中,接受PLD治疗的所有患者中约50%出现了PPE,约20%出现了3级PPE。与任何与之相关的药物一样,PPE的病理生理学尚未完全了解。评估与PLD特异性相关的PPE发生情况的研究尚未完全阐明其机制;然而,数据支持汗液中药物排泄和局部压力在其中所起的作用。当发生PPE时,关于改变PLD给药的临床干预措施包括降低剂量、减少给药频率,最终停药,这会对治疗效果产生多种影响。本文将综述有关与PLD相关的PPE的病因及潜在管理策略的现有数据。

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