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使用阿仑单抗/低剂量放疗进行非清髓性干细胞移植以治愈并改善镰状细胞病成人患者的生活质量

Nonmyeloablative Stem Cell Transplantation with Alemtuzumab/Low-Dose Irradiation to Cure and Improve the Quality of Life of Adults with Sickle Cell Disease.

作者信息

Saraf Santosh L, Oh Annie L, Patel Pritesh R, Jalundhwala Yash, Sweiss Karen, Koshy Matthew, Campbell-Lee Sally, Gowhari Michel, Hassan Johara, Peace David, Quigley John G, Khan Irum, Molokie Robert E, Hsu Lewis L, Mahmud Nadim, Levinson Dennis J, Pickard A Simon, Garcia Joe G N, Gordeuk Victor R, Rondelli Damiano

机构信息

Division of Hematology/Oncology, University of Illinois Hospital and Health Sciences System, Chicago, Illinois; University of Illinois Sickle Cell Center, Department of Medicine, University of Illinois Hospital & Health Sciences System, Chicago, Illinois; University of Illinois Cancer Center, Chicago, Illinois.

Division of Hematology/Oncology, University of Illinois Hospital and Health Sciences System, Chicago, Illinois.

出版信息

Biol Blood Marrow Transplant. 2016 Mar;22(3):441-8. doi: 10.1016/j.bbmt.2015.08.036. Epub 2015 Sep 5.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is rarely performed in adult patients with sickle cell disease (SCD). We utilized the chemotherapy-free, alemtuzumab/total body irradiation 300 cGy regimen with sirolimus as post-transplantation immunosuppression in 13 high-risk SCD adult patients between November 2011 and June 2014. Patients received matched related donor (MRD) granulocyte colony-stimulating factor-mobilized peripheral blood stem cells, including 2 cases that were ABO incompatible. Quality-of-life (QoL) measurements were performed at different time points after HSCT. All 13 patients initially engrafted. A stable mixed donor/recipient chimerism was maintained in 12 patients (92%), whereas 1 patient not compliant with sirolimus experienced secondary graft failure. With a median follow-up of 22 months (range, 12 to 44 months) there was no mortality, no acute or chronic graft-versus-host disease (GVHD), and no grades 3 or 4 extramedullary toxicities. At 1 year after transplantation, patients with stable donor chimerism have normalized hemoglobin concentrations and improved cardiopulmonary and QoL parameters including bodily pain, general health, and vitality. In 4 patients, sirolimus was stopped without rejection or SCD-related complications. These results underscore the successful use of a chemotherapy-free regimen in MRD HSCT for high-risk adult SCD patients and demonstrates a high cure rate, absence of GVHD or mortality, and improvement in QoL including the applicability of this regimen in ABO mismatched cases (NCT number 01499888).

摘要

异基因造血干细胞移植(HSCT)在成年镰状细胞病(SCD)患者中很少进行。2011年11月至2014年6月期间,我们对13例高危成年SCD患者采用了无化疗的阿仑单抗/300 cGy全身照射方案,并使用西罗莫司作为移植后免疫抑制。患者接受了匹配的相关供体(MRD)粒细胞集落刺激因子动员的外周血干细胞,其中包括2例ABO血型不相容的病例。在HSCT后的不同时间点进行了生活质量(QoL)测量。所有13例患者均最初植入成功。12例患者(92%)维持了稳定的供体/受体混合嵌合状态,而1例未遵医嘱使用西罗莫司的患者发生了继发性移植失败。中位随访22个月(范围12至44个月),无死亡病例,无急性或慢性移植物抗宿主病(GVHD),也无3级或4级髓外毒性。移植后1年,供体嵌合状态稳定的患者血红蛋白浓度恢复正常,心肺功能和QoL参数得到改善,包括身体疼痛、总体健康和活力。4例患者停用西罗莫司后未出现排斥反应或SCD相关并发症。这些结果强调了无化疗方案在MRD HSCT治疗高危成年SCD患者中的成功应用,并显示出高治愈率、无GVHD或死亡,以及QoL的改善,包括该方案在ABO血型不匹配病例中的适用性(NCT编号01499888)。

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