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作 者:朱尊民[1] Anthony P Schwarer Miroslai Kapuscinski
机构地区:[1]河南省人民医院血液科,郑州市450003 [2]澳大利亚墨尔本阿尔福德医院骨髓移植中心
出 处:《医药论坛杂志》2005年第14期1-2,共2页Journal of Medical Forum
摘 要:目的评价非清髓性造血干细胞移植(NMSCT)的疗效及供受者嵌合体的检测。方法用氟达拉宾25mg/m2,-5d^-1d、马法兰140mg/m2?1d、抗胸腺细胞球蛋白15mg/(kg.d)-4d^+5d作为预处理方案,环胞霉素3mg/(kg.d),麦考芬酸脂15mg/(kg.d)用于GVHD的预防。为17例患者做了,并对嵌合体进行检测。结果17例患者达到了早期植入,中性粒细胞恢复至0.5×109/L,中位时间为13d,血小板恢复至30×109/L,中位时间为17d。全部供者粒细胞嵌合体形成中位时间为4周,全部供者T细胞形成中位时间为8周。结论应用氟达拉宾、马法兰、抗胸腺细胞球蛋白作为非清髓性造血干细胞移植预处理方案,可获得供者早期植入,不良反应少。Objective To evaluate the effect transplantation (NMSCT)and test chimerism. Methods of non -myeloablative allo -genic stem cell 17 patients have been done NMSCT with Fludarabine(25mg/m^2, -5d ~ - 1d), Melphalan ( 140mg/m^2 - 1d) and ATG ( 15mg/( kg. d) - 4d ~ + 5d), condition regimen ( cyclosporine 3 mg/( kg. d ) Myecophine 15 mg/( kg. d ) for GVHD prevention ) and its chimerism have been tested. Results 17 patients were engrafted early. The median time to neutrophil 0.5 ×^109/L and platelet 30 × 10^9/L was 13 and 17days post - transplant respectively. The median time to full donor myeloid cell and T cell chimerism was 4 and 8 weeks respectively. Conclusion Fludarabine melphalan and ATG as a conditioning regimen for NMSCT is safe and is engrafted early.
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