The effectiveness of tacrolimus and minidose methotrexate in the prevention of acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation in children: a single-center study in Korea.

The Korean Journal of Hematology Pub Date : 2012-06-01 Epub Date: 2012-06-26 DOI:10.5045/kjh.2012.47.2.113
Seong Shik Park, So Eun Jun, Young Tak Lim
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引用次数: 5

Abstract

Background Knowledge of the roles of tacrolimus and minidose methotrexate (MTX) in the prevention of acute graft-versus-host disease (aGVHD) in pediatric allogeneic hematopoietic stem cell transplantation (HSCT) is limited. We retrospectively evaluated the engraftment status, incidence of aGVHD and chronic GVHD (cGVHD), and toxicities of tacrolimus and minidose MTX in aGVHD prophylaxis in children undergoing allogeneic HSCT. Methods Seventeen children, who underwent allogeneic HSCT and received tacrolimus and minidose MTX as GVHD prophylaxis from March 2003 to February 2011, were reviewed retrospectively. All the patients received tacrolimus since the day before transplantation at a dose of 0.03 mg/kg/day and MTX at a dose of 5 mg/m2 on days 1, 3, 6, and 11. Results Of the 17 patients, 9 received human leukocyte antigen (HLA)-matched related donor transplants, and 8 received HLA-matched, or partially mismatched unrelated donor transplants. The median time for follow-up was 55 months. The incidence of aGVHD in the related and unrelated donor groups was 22.2% and 42.9%, respectively. cGVHD was not observed. To maintain therapeutic blood levels of tacrolimus, the younger group (<8 years of age) required an increased mean dose compared to the older group (≥8 years) (P=0.0075). The adverse events commonly associated with tacrolimus included hypomagnesemia (88%), nephrotoxicity (23%), and hyperglycemia (23%). Conclusion Tacrolimus and minidose MTX were well tolerated and effective in GVHD prophylaxis in pediatric patients undergoing allogeneic HSCT. Children <8 years of age undergoing HSCT required increased doses of tacrolimus to achieve therapeutic levels.

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他克莫司和小剂量甲氨蝶呤预防儿童异基因造血干细胞移植后急性移植物抗宿主病的有效性:韩国单中心研究
背景:关于他克莫司和甲氨蝶呤(MTX)在儿童同种异体造血干细胞移植(HSCT)中预防急性移植物抗宿主病(aGVHD)的作用的知识是有限的。我们回顾性评估了同种异体造血干细胞移植儿童的移植状态、aGVHD和慢性GVHD (cGVHD)的发病率,以及他克莫司和小剂量MTX预防aGVHD的毒性。方法:回顾性分析2003年3月至2011年2月接受同种异体造血干细胞移植并给予他克莫司和小剂量甲氨蝶呤预防GVHD的17例患儿。所有患者在移植前一天开始接受他克莫司0.03 mg/kg/天的剂量和MTX 5 mg/m(2)的剂量,分别在第1、3、6和11天。结果:17例患者中,9例接受HLA匹配的相关供体移植,8例接受HLA匹配或部分不匹配的非相关供体移植。中位随访时间为55个月。相关供体组和非相关供体组的aGVHD发生率分别为22.2%和42.9%。未观察到cGVHD。结论:他克莫司和小剂量MTX在接受同种异体造血干细胞移植的儿童患者中具有良好的耐受性和有效的GVHD预防。孩子们
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