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异基因干细胞移植后移植前预防性使用膦甲酸钠的安全性。

Safety of pre-engraftment prophylactic foscarnet administration after allogeneic stem cell transplantation.

作者信息

Ishiyama K, Katagiri T, Ohata K, Hosokawa K, Kondo Y, Yamazaki H, Takami A, Nakao S

机构信息

Department of Cellular Transplantation Biology, Division of Cancer Medicine, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.

出版信息

Transpl Infect Dis. 2012 Feb;14(1):33-9. doi: 10.1111/j.1399-3062.2011.00662.x. Epub 2011 Jul 28.

DOI:10.1111/j.1399-3062.2011.00662.x
PMID:21794043
Abstract

Human herpesvirus-6 (HHV-6) is a major cause of limbic encephalitis with a dismal prognosis after allogeneic hematopoietic stem cell transplantation (SCT). Because our previous trial of preemptive therapy with foscarnet sodium (phosphonoformic acid; PFA) failed to prevent HHV-6 encephalitis, we conducted a prospective study to examine the safety of prophylactic PFA administration and elucidate the changes in the plasma HHV-6 DNA levels in the early post-SCT period. Plasma HHV-6 DNA was measured thrice weekly from day 6. PFA, 90 mg/kg/day, was administered from days 7 to 21 after bone marrow or peripheral blood SCT and to day 25 after umbilical cord blood transplantation. Of the 10 patients enrolled, 2 dropped out of the study, 1 because of early death, and 1 with a low glomerular filtration rate. Grade 3 or greater adverse events occurred in 9 of the 10 prophylactic PFA patients and in 7 of the 10 control patients who had clinical backgrounds similar to the study subjects and underwent SCT during the same period. Neurological disorders developed in none of the study subjects but in 4 of the 10 control patients, including 2 with HHV-6 encephalitis. HHV-6 reactivation occurred in 3 of the 10 study subjects. The prophylactic PFA regimen was thus safe and it may reduce the risk of limbic encephalitis, but is not considered to be potent enough to prevent HHV-6 reactivation.

摘要

人类疱疹病毒6型(HHV-6)是异基因造血干细胞移植(SCT)后边缘性脑炎的主要病因,预后不佳。由于我们之前使用膦甲酸钠(磷甲酸;PFA)进行抢先治疗的试验未能预防HHV-6脑炎,我们进行了一项前瞻性研究,以检验预防性给予PFA的安全性,并阐明SCT后早期血浆HHV-6 DNA水平的变化。从第6天开始,每周三次测量血浆HHV-6 DNA。在骨髓或外周血SCT后的第7至21天以及脐带血移植后的第25天,给予PFA,剂量为90 mg/kg/天。在纳入的10例患者中,2例退出研究,1例因早期死亡,1例肾小球滤过率低。在10例接受预防性PFA治疗的患者中,9例发生了3级或更严重的不良事件;在10例具有与研究对象相似临床背景且在同一时期接受SCT的对照患者中,7例发生了此类事件。研究对象中无一例发生神经疾病,但10例对照患者中有4例发生,其中2例患有HHV-6脑炎。10例研究对象中有3例发生HHV-6再激活。因此,预防性PFA方案是安全的,可能会降低边缘性脑炎的风险,但被认为不足以预防HHV-6再激活。

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