Cho Byung-Sik, Kim Yoo-Jin, Cho Seok-Goo, Kim Sung-Yong, Eom Ki-Seong, Kim Hee-Je, Lee Seok, Min Chang-Ki, Kim Dong-Wook, Lee Jong-Wook, Min Woo-Sung, Kim Chun-Choo
Catholic Hematopoietic Stem Cell Transplantation Center, The Catholic University of Korea, Seoul, Korea.
Int J Hematol. 2007 Jun;85(5):446-55. doi: 10.1532/IJH97.A30616.
Allogeneic hematopoietic stem cell transplantation following reduced-intensity stem cell transplantation (RIST) has enabled the treatment of older or medically infirm patients with myeloid malignancies; however, determining the value of RIST outcomes for myelodysplastic syndrome (MDS) is difficult because of the heterogeneity of the diseases included in most trials. To define the role of RIST in MDS, we performed RIST for 22 consecutive patients who had de novo MDS as classified by World Health Organization (WHO) criteria and who received an allograft with fludarabine/busulfan (Busulfex) or fludarabine/Busulfex/antithymocyte globulin (ATG) conditioning. Nineteen patients (86.4%) achieved engraftment. At a median follow-up of 18.9 months (range, 13.1-24.8 months), the estimated 2-year rates of overall survival, event-free survival (EFS), transplantation-related mortality, and relapse were 78.7%, 67.7%, 12.6%, and 22.5%, respectively. Acute graft-versus-host disease (GVHD) greater than grade II developed in 3 patients (15.8%). Chronic GVHD developed in 10 patients (55.6%), none of whom received ATG as a conditioning regimen. Variables influencing EFS were chronic GVHD, marrow blasts before transplantation, and the WHO criteria. The present study clarifies the benefits of the fludarabine/Busulfex-based conditioning regimen for de novo MDS diagnosed according to the WHO criteria and shows that chronic GVHD appears to have a beneficial effect on survival rates, which are strongly associated with graft-versus-tumor effects.
减低强度干细胞移植(RIST)后的异基因造血干细胞移植已能够治疗老年或身体虚弱的髓系恶性肿瘤患者;然而,由于大多数试验所纳入疾病的异质性,确定RIST治疗骨髓增生异常综合征(MDS)的疗效价值具有一定难度。为明确RIST在MDS中的作用,我们对22例符合世界卫生组织(WHO)标准的初诊MDS患者连续进行了RIST治疗,这些患者接受了氟达拉滨/白消安(白舒非)或氟达拉滨/白消安/抗胸腺细胞球蛋白(ATG)预处理的同种异体移植。19例患者(86.4%)实现了植入。在中位随访18.9个月(范围13.1 - 24.8个月)时,估计的2年总生存率、无事件生存率(EFS)、移植相关死亡率和复发率分别为78.7%、67.7%、12.6%和22.5%。3例患者(15.8%)发生了大于II级的急性移植物抗宿主病(GVHD)。10例患者(55.6%)发生了慢性GVHD,其中无一例接受ATG作为预处理方案。影响EFS的变量为慢性GVHD、移植前骨髓原始细胞以及WHO标准。本研究阐明了基于氟达拉滨/白消安的预处理方案对根据WHO标准诊断的初诊MDS的益处,并表明慢性GVHD似乎对生存率有有益影响,这与移植物抗肿瘤效应密切相关。