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拓扑替康治疗获得性免疫缺陷综合征相关的进行性多灶性白质脑病。

Topotecan in the treatment of acquired immunodeficiency syndrome-related progressive multifocal leukoencephalopathy.

作者信息

Royal W, Dupont B, McGuire D, Chang L, Goodkin K, Ernst T, Post M J, Fish D, Pailloux G, Poncelet H, Concha M, Apuzzo L, Singer E

机构信息

Neuroscience Institute, Morehouse School of Medicine, Atlanta, Georgia 30310-1495, USA.

出版信息

J Neurovirol. 2003 Jun;9(3):411-9. doi: 10.1080/13550280390201740.

Abstract

Progressive multifocal leukoencephalopathy (PML) affects about 1 in 20 individuals with the acquired immunodeficiency syndrome (AIDS) and has been associated with poor survival. This report describes the results of a phase II clinical trial using the drug topotecan, a semisynthetic analogue of camptothecan, administered to a cohort of subjects with AIDS-related PML. Data were evaluated on 11 of 12 subjects enrolled in the study. Three responded to therapy. Additionally, one patient was treated off-protocol and showed a response to treatment. Progression occurred after the first course; however, a partial response was noted after five courses. One study patient died from accidental overdose of topotecan. Overall, responders had higher pretreatment Karnofsky and lower Kurtzke expanded disability status scale scores than nonresponders. The most frequent toxicities were hematologic (anemia, neutropenia, and thrombocytopenia). Five patients had dose delays; all delays were due to hematologic adverse events. This study demonstrates that topotecan treatment may be associated with decreased lesion size and prolonged survival from the infection. Because of the small number of subjects in the study, further studies are required to evaluate the efficacy of topotecan in treating this disease.

摘要

进行性多灶性白质脑病(PML)在每20名获得性免疫缺陷综合征(AIDS)患者中约有1人受影响,且与生存率低相关。本报告描述了一项II期临床试验的结果,该试验使用喜树碱的半合成类似物拓扑替康,对一组患有AIDS相关PML的受试者进行给药。对研究中登记的12名受试者中的11名的数据进行了评估。3名受试者对治疗有反应。此外,1名患者接受了非方案治疗并显示对治疗有反应。在第一个疗程后病情进展;然而,在五个疗程后观察到部分缓解。1名研究患者死于拓扑替康意外过量。总体而言,有反应者的治疗前卡诺夫斯基评分较高,而库尔茨克扩展残疾状态量表评分低于无反应者。最常见的毒性是血液学毒性(贫血、中性粒细胞减少和血小板减少)。5名患者出现剂量延迟;所有延迟均归因于血液学不良事件。本研究表明,拓扑替康治疗可能与病变大小减小和感染导致的生存期延长有关。由于研究中的受试者数量较少,需要进一步研究来评估拓扑替康治疗这种疾病的疗效。

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