Srinivasan Ramaprasad, Takahashi Yoshiyuki, McCoy J Philip, Espinoza-Delgado Igor, Dorrance Colleen, Igarashi Takehito, Lundqvist Andreas, Barrett A John, Young Neal S, Geller Nancy, Childs Richard W
Urologic Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
Br J Haematol. 2006 May;133(3):305-14. doi: 10.1111/j.1365-2141.2006.06019.x.
Allogeneic haematopoietic cell transplantation (HCT) can cure a variety of non-malignant haematological disorders. Although transplant outcomes for selected patients with severe aplastic anaemia (SAA) and paroxysmal nocturnal haemoglobinuria (PNH) have improved, older age, allo-immunisation from transfusions, prior immunosuppressive therapy and a prolonged time from diagnosis to transplantation are associated with worse outcome. Because of its potent immunosuppressive effects, we investigated a fludarabine-based non-myeloablative conditioning regimen in patients with transfusion-dependent non-malignant haematological disorders at increased risk for graft rejection with conventional transplant conditioning. Twenty-six patients with transfusion dependent/anti-thymocyte globulin (ATG)-refractory SAA, PNH or pure red cell aplasia underwent HCT from a human leucocyte antigen (HLA)-compatible relative. Transplant conditioning consisted of cyclophosphamide (120 mg/kg) and fludarabine (125 mg/m2) with or without ATG. Ciclosporine, alone or combined with mycophenolate mofetil or methotrexate, was used as graft-versus-host disease (GVHD) prophylaxis. All patients achieved durable engraftment and transfusion-independence. Twenty-four of 26 patients are alive at a median of 21 months following transplantation. Although a high cumulative incidence of acute (65% grades II-IV, 54% grades III-IV) and chronic GVHD (56%) was observed, only one patient died from transplant-related causes (cumulative incidence 7%). These data show that HCT following fludarabine-based non-myeloablative conditioning results in durable engraftment and excellent survival in SAA and PNH patients at high risk for graft rejection.
异基因造血细胞移植(HCT)可治愈多种非恶性血液系统疾病。尽管部分严重再生障碍性贫血(SAA)和阵发性睡眠性血红蛋白尿(PNH)患者的移植结局有所改善,但年龄较大、输血导致的同种免疫、既往免疫抑制治疗以及从诊断到移植的时间延长与较差的结局相关。由于其强大的免疫抑制作用,我们对依赖输血的非恶性血液系统疾病患者采用了基于氟达拉滨的非清髓性预处理方案,这些患者因传统移植预处理而发生移植物排斥的风险增加。26例依赖输血/抗胸腺细胞球蛋白(ATG)难治性SAA、PNH或纯红细胞再生障碍性贫血患者接受了来自人类白细胞抗原(HLA)相合亲属的HCT。移植预处理包括环磷酰胺(120 mg/kg)和氟达拉滨(125 mg/m²),可加用或不加用ATG。单独使用环孢素或与霉酚酸酯或甲氨蝶呤联合使用,作为移植物抗宿主病(GVHD)的预防措施。所有患者均实现了持久植入和输血独立。26例患者中有24例在移植后中位21个月时存活。尽管观察到急性(65%为II-IV级,54%为III-IV级)和慢性GVHD(56%)的累积发生率较高,但仅有1例患者死于移植相关原因(累积发生率7%)。这些数据表明,基于氟达拉滨的非清髓性预处理后的HCT可使SAA和PNH患者实现持久植入并获得良好生存,这些患者发生移植物排斥的风险较高。