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甲氨蝶呤与环孢素A作为单一药物用于预防接受来自 HLA 同型同胞的异基因骨髓移植的血液系统恶性肿瘤儿科患者的移植物抗宿主病:日本单中心分析

Methotrexate vs Cyclosporin A as a single agent for graft-versus-host disease prophylaxis in pediatric patients with hematological malignancies undergoing allogeneic bone marrow transplantation from HLA-identical siblings: a single-center analysis in Japan.

作者信息

Koga Y, Nagatoshi Y, Kawano Y, Okamura J

机构信息

Section of Pediatrics, National Kyushu Cancer Center, Fukuoka, Japan.

出版信息

Bone Marrow Transplant. 2003 Jul;32(2):171-6. doi: 10.1038/sj.bmt.1704051.

Abstract

The efficacy of methotrexate (MTX) as a single graft-versus-host disease (GVHD) prophylaxis agent was compared to that of cyclosporin A (CSA) in 62 pediatric patients (median age: 8 years) with hematological malignancies who had undergone bone marrow transplantation (BMT) from HLA-identical sibling donors at National Kyushu Cancer Center since 1977. In all, 30 patients received MTX by intravenous bolus injection, with a dose of 15 mg/m(2) on day +1, followed by 10 mg/m(2) on days +3, +6, and +11, and then once a week until day +100. A total of 32 patients were treated with CSA, which was given intravenously in the early stages and orally thereafter until day +100, and then gradually tapered and stopped 6 months after BMT. There were no differences between the groups in terms of rates of hematopoietic recovery after BMT. The probabilities of acute GVHD (grades II-IV) and chronic GVHD were 29.6 vs 40.6% (P=0.294) and 19 vs 20% (MTX vs CSA), respectively. Relapse rates and event-free survival were identical. These results suggest that MTX and CSA were equally effective when given after BMT in Japanese pediatric patients with hematological malignancies. Since MTX was given over a shorter time than CSA, it might be more practical in the management of such patients.

摘要

自1977年以来,在国立九州癌症中心,对62例患有血液系统恶性肿瘤且接受了来自 HLA 相同同胞供体骨髓移植(BMT)的儿科患者(中位年龄:8岁),比较了甲氨蝶呤(MTX)作为单一移植物抗宿主病(GVHD)预防药物与环孢素A(CSA)的疗效。总共30例患者通过静脉推注接受MTX治疗,在 +1天剂量为15mg/m²,随后在 +3、+6和 +11天为10mg/m²,然后每周一次直至 +100天。共有32例患者接受CSA治疗,早期静脉给药,之后口服直至 +100天,然后逐渐减量并在BMT后6个月停药。两组在BMT后造血恢复率方面无差异。急性GVHD(II - IV级)和慢性GVHD的发生率分别为29.6%对40.6%(P = 0.294)和19%对20%(MTX对CSA)。复发率和无事件生存率相同。这些结果表明,在日本患有血液系统恶性肿瘤的儿科患者中,BMT后给予MTX和CSA同样有效。由于MTX的给药时间比CSA短,在这类患者的管理中可能更实用。

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