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低剂量阿仑单抗(Campath)用于CD52阳性恶性肿瘤的清髓性异基因干细胞移植:急性移植物抗宿主病发生率降低且具有独特的药代动力学。

Low-dose alemtuzumab (Campath) in myeloablative allogeneic stem cell transplantation for CD52-positive malignancies: decreased incidence of acute graft-versus-host-disease with unique pharmacokinetics.

作者信息

Khouri I F, Albitar M, Saliba R M, Ippoliti C, Ma Y C, Keating M J, Champlin R E

机构信息

Department of Blood and Marrow Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Bone Marrow Transplant. 2004 Apr;33(8):833-7. doi: 10.1038/sj.bmt.1704435.

Abstract

Alemtuzumab is effective in reducing the risk of acute graft-versus-host disease (GVHD) after allogeneic stem cell transplantation (ASCT). Alemtuzumab may also delay immune reconstitution and reduce graft-versus-leukemia effects. The optimal dose has not been established. We investigated engraftment, acute GVHD incidence and severity, and pharmacokinetics of alemtuzumab associated with the use of low-dose alemtuzumab/cyclophosphamide/total body irradiation and ASCT for patients with aggressive CD52-positive hematologic malignancies. In all, 12 patients were treated. Alemtuzumab 10 mg daily on days -7 to -3 was given intravenously. Tacrolimus and methotrexate were used for GVHD prophylaxis. Alemtuzemab was not detected in any of the 36 sequential serum samples tested between days -1 and +21 of transplant. All patients engrafted rapidly; the median time to an absolute neutrophil count >0.5 x 10(9)/l was 14 days (range 11-17 days), and the median time to a platelet count >20 x 10(9)/l was 16 days (range 6-30 days). By 1 month after transplant, nine patients had 100% donor chimerism, while three had mixed donor chimerism. At 3 months, 11 had achieved 100% donor chimerism. No cases of grade III/IV acute GVHD occurred. At a median follow-up interval of 14.7 months (range 4-24), seven patients remained alive, and five remained free of disease.

摘要

阿仑单抗在降低异基因干细胞移植(ASCT)后急性移植物抗宿主病(GVHD)风险方面有效。阿仑单抗也可能延迟免疫重建并降低移植物抗白血病效应。最佳剂量尚未确定。我们研究了与低剂量阿仑单抗/环磷酰胺/全身照射及ASCT联合使用时阿仑单抗的植入情况、急性GVHD的发生率和严重程度以及药代动力学,用于治疗侵袭性CD52阳性血液系统恶性肿瘤患者。总共治疗了12例患者。在移植前第-7天至-3天,每天静脉给予阿仑单抗10毫克。使用他克莫司和甲氨蝶呤预防GVHD。在移植后第-1天至+21天期间检测的36份连续血清样本中,均未检测到阿仑单抗。所有患者均迅速植入;绝对中性粒细胞计数>0.5×10⁹/L的中位时间为14天(范围11 - 17天),血小板计数>20×10⁹/L的中位时间为16天(范围6 - 30天)。移植后1个月时,9例患者供体嵌合率达100%,3例为混合供体嵌合。3个月时,11例达到100%供体嵌合。未发生III/IV级急性GVHD病例。中位随访间隔为14.7个月(范围4 - 24个月),7例患者存活,5例无疾病。

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