Lalezari J P, Kuppermann B D
Department of Medicine, University of California, San Francisco 94115, U.S.A.
J Acquir Immune Defic Syndr Hum Retrovirol. 1997;14 Suppl 1:S27-31. doi: 10.1097/00042560-199700001-00006.
Cidofovir (Vistide, HPMPC) is a nucleotide analogue with potent in vitro activity against cytomegalovirus (CMV) that was recently licensed for treatment of patients with acquired immunodeficiency syndrome (AIDS) and CMV retinitis. Cidofovir's prolonged intracellular half-life permits dosing once every 2 weeks for maintenance treatment. The treatment-limiting toxicity of cidofovir is dose- and schedule-dependent nephrotoxicity affecting renal proximal convoluted tubule cells. A treatment regimen that includes concomitant administration of oral probenecid, intravenous hydration, and careful preinfusion evaluation of renal function with conservative dose modification has reduced cidofovir-associated nephrotoxicity. Preliminary results of clinical studies of cidofovir in AIDS patients with newly diagnosed and relapsing CMV retinitis are described.
西多福韦(Vistide,HPMPC)是一种核苷酸类似物,在体外对巨细胞病毒(CMV)具有强大活性,最近已获许可用于治疗获得性免疫缺陷综合征(AIDS)患者及CMV视网膜炎。西多福韦在细胞内的半衰期较长,维持治疗时每2周给药一次即可。西多福韦的治疗限制性毒性是剂量和给药方案依赖性肾毒性,会影响肾近端曲管细胞。一种治疗方案包括同时口服丙磺舒、静脉补液,并通过保守的剂量调整对肾功能进行仔细的输注前评估,该方案已降低了与西多福韦相关的肾毒性。本文描述了西多福韦在新诊断和复发性CMV视网膜炎AIDS患者中的临床研究初步结果。