Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Blood. 2010 Dec 23;116(26):5824-31. doi: 10.1182/blood-2010-04-282392. Epub 2010 Sep 20.
Recent experience suggests that reduced-intensity conditioning (RIC) regimens can improve the outcomes of patients with hemophagocytic lymphohistiocytosis (HLH) undergoing allogeneic hematopoietic cell transplantation (HCT). However, studies directly comparing RIC to myeloablative conditioning (MAC) regimens are lacking. Forty patients with HLH underwent allogeneic HCT between 2003-2009 at Cincinnati Children's Hospital. Fourteen patients received MAC consisting of busulfan, cyclophosphamide, and antithymocyte globulin plus or minus etoposide. Twenty-six patients received RIC consisting of fludarabine, melphalan, and alemtuzumab. All patients engrafted. Acute graft-versus-host disease grades II to III occurred in 14% of MAC patients and 8% of RIC patients (P = .3171). Posttransplantation mixed donor/recipient chimerism developed in 18% of MAC patients and 65% of RIC patients (P = .0110). The majority of patients with mixed chimerism received intervention with reduction of immune suppression plus or minus donor lymphocyte infusion or stem cell boost, which stabilized or increased donor contribution to hematopoiesis and prevented relapse of HLH in all but 1 patient. Grade II to III graft-versus-host disease occurred in 5 of 14 RIC patients after donor lymphocyte infusion. The overall estimated 3-year survival after HCT was 43% (confidence interval = ± 26%) for MAC patients and 92% (confidence interval = ± 11%) for RIC patients (P = .0001). We conclude that RIC significantly improves the outcome of patients with HLH undergoing allogeneic HCT.
最近的经验表明,降低强度的调理(RIC)方案可以改善接受异基因造血细胞移植(HCT)的噬血细胞性淋巴组织细胞增多症(HLH)患者的结局。然而,缺乏直接比较 RIC 与清髓性调理(MAC)方案的研究。
2003 年至 2009 年间,辛辛那提儿童医院的 40 例 HLH 患者接受了异基因 HCT。14 例患者接受了 MAC,方案为白消安、环磷酰胺和抗胸腺细胞球蛋白,加或不加依托泊苷。26 例患者接受了 RIC,方案为氟达拉滨、美法仑和阿仑单抗。所有患者均植活。MAC 患者中有 14%发生 II 级至 III 级急性移植物抗宿主病,RIC 患者中有 8%(P =.3171)。MAC 患者中有 18%和 RIC 患者中有 65%发生移植后混合供体/受者嵌合体(P =.0110)。大多数混合嵌合体患者接受了减少免疫抑制加或不加供者淋巴细胞输注或干细胞加强的干预,这稳定或增加了供者对造血的贡献,并防止了除 1 例患者外的 HLH 复发。在 14 例接受 RIC 的患者中,有 5 例在接受供者淋巴细胞输注后发生 II 级至 III 级移植物抗宿主病。MAC 患者的总估计 3 年生存率为 43%(置信区间=±26%),RIC 患者为 92%(置信区间=±11%)(P =.0001)。我们的结论是,RIC 显著改善了接受异基因 HCT 的 HLH 患者的结局。