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