Hunter A E, Bessell E M, Russell N H
Department of Haematology, City Hospital, Nottingham, UK.
Bone Marrow Transplant. 1992 Nov;10(5):431-4.
Although the combination of cyclosporin A (CYA) and methotrexate has been reported to reduce the incidence of acute GVHD in patients undergoing allogeneic BMT for leukaemia, it has been associated with a higher risk of leukaemic relapse. Since 1987 we have used the combination of CYA and methotrexate for GVHD prophylaxis in 24 patients undergoing allogeneic BMT for leukaemia or myelodysplasia. Over the first 50 days post-transplantation, CYA dosage was adjusted to keep within a therapeutic range of 95-205 ng/ml. This resulted in a 60% reduction in CYA dosage by day 50 post-transplant compared to the original Seattle protocol. Despite the low dosage of CYA administered, the incidence of acute GVHD was only 25% with no patient having greater than grade I GVHD. There have been no leukaemic relapses in low risk patients. The results indicate that decreasing CYA dosage does not increase the incidence of GVHD but may reduce the risk of leukaemic relapse following allogeneic BMT.
尽管据报道,环孢素A(CYA)与甲氨蝶呤联合使用可降低接受异基因骨髓移植治疗白血病患者的急性移植物抗宿主病(GVHD)发生率,但它与白血病复发风险较高相关。自1987年以来,我们已将CYA与甲氨蝶呤联合用于24例接受异基因骨髓移植治疗白血病或骨髓增生异常综合征的患者预防GVHD。在移植后的前50天内,调整CYA剂量以使其保持在95 - 205 ng/ml的治疗范围内。与最初的西雅图方案相比,这导致移植后第50天时CYA剂量降低了60%。尽管给予的CYA剂量较低,但急性GVHD的发生率仅为25%,没有患者的GVHD超过I级。低风险患者中没有白血病复发情况。结果表明,降低CYA剂量不会增加GVHD的发生率,但可能降低异基因骨髓移植后白血病复发的风险。