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儿童干细胞移植中预防移植物抗宿主病采用每日两次静脉推注他克莫司。

Twice daily i.v. bolus tacrolimus infusion for GVHD prophylaxis in children undergoing stem cell transplantation.

机构信息

Division of Pediatric Hematology/Oncology/BMT and Pharmacy, Nationwide Children's Hospital, The Ohio State University, Columbus, OH 43205, USA.

出版信息

Bone Marrow Transplant. 2012 Nov;47(11):1415-8. doi: 10.1038/bmt.2012.59. Epub 2012 Apr 9.

DOI:10.1038/bmt.2012.59
PMID:22484323
Abstract

Tacrolimus is routinely administered for GVHD prophylaxis as a 24-h continuous infusion that requires a dedicated i.v. line and thus becomes logistically difficult to administer, especially in young pediatric patients. We investigated the safety and efficacy of twice daily bolus infusions of i.v. tacrolimus in 33 children undergoing hematopoietic stem cell transplantation (HSCT) at our institution. Tacrolimus was started at an initial dose of 0.015 mg/kg i.v. bolus administered as a 2-h infusion and then given at every 12 h to maintain a trough drug level between 5-15 ng/mL. Patients also received short-course MTX (66%) or mycophenolate mofetil (34%) in combination with tacrolimus. No acute infusional toxicities were observed with bolus infusions of i.v. tacrolimus. Nephrotoxicity occurred in 14/33 (42%) patients and 48% developed hypertension (HT). Almost all (94%) patients required magnesium supplements to maintain magnesium (Mg) levels 1.5 mg/dL. In all, 3 (9%) patients developed severe sinusoidal obstruction syndrome (SOS). One patient developed posterior reversible leuko-encephalopathy syndrome (PRES) and one additional patient had tremors. The prevelance of these side-effects was similar to those reported for continuous i.v. administration. In all, 28% of the evaluable patients developed acute GVHDgrade II, though the incidence of severe (grade III-IV) GVHD was only 7%. These results suggest that intermittent bolus i.v. tacrolimus administration is a safe and effective method of GVHD prophylaxis in children.

摘要

他克莫司常规用于移植物抗宿主病(GVHD)预防,采用 24 小时持续输注方式,这需要一条专用的静脉输液管路,因此在给药方面具有很大的挑战性,尤其是在年幼的儿科患者中。我们研究了在我院接受造血干细胞移植(HSCT)的 33 例儿童中,每日两次静脉推注他克莫司的安全性和有效性。他克莫司初始剂量为 0.015mg/kg,静脉推注 2 小时,然后每 12 小时给药 1 次,以维持谷浓度在 5-15ng/ml 之间。患者还接受了短程甲氨蝶呤(66%)或霉酚酸酯(34%)联合他克莫司治疗。静脉推注他克莫司无急性输注毒性。14/33(42%)例患者发生肾毒性,48%发生高血压(HT)。几乎所有(94%)患者需要补充镁以维持镁(Mg)水平 1.5mg/dL。共有 3(9%)例患者发生严重肝窦阻塞综合征(SOS)。1 例患者发生可逆性后部白质脑病综合征(PRES),另有 1 例患者出现震颤。这些副作用的发生率与连续静脉输注时的报告相似。所有患者中,28%的可评估患者发生急性移植物抗宿主病 Ⅱ级,而严重(Ⅲ-Ⅳ级)GVHD 的发生率仅为 7%。这些结果表明,间断静脉推注他克莫司是儿童预防移植物抗宿主病的一种安全有效的方法。

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