Solh Melhem M, Bashey Asad, Solomon Scott R, Morris Lawrence E, Zhang Xu, Brown Stacey, Holland H Kent
Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, USA.
Center for Clinical and Translational Sciences, University of Texas Health Science Center at Houston, Houston, USA.
Bone Marrow Transplant. 2018 May;53(5):576-583. doi: 10.1038/s41409-017-0076-2. Epub 2018 Jan 15.
Allogeneic hematopoietic cell transplantation (HCT) is associated with significant morbidity and mortality especially in the first year after HCT. In this study, we examine the long-term outcomes of patients who survived at least one year post HCT without evidence of relapse. We analyzed the records for 389 consecutive patients receiving an allogeneic transplant from 2005 to 2016 from a MRD, MUD, or haploidentical donor, who were alive and disease free at one year post-transplant. Patient characteristics and outcome parameters were extracted from our institutional database where they had been prospectively entered. A total of 389 patients met the selection criteria with donor graft including MRD 37%, MUD 39%, and Haploidenitcal relative 24%. The median follow-up of survivors from time of HCT was 48.2 months. The median overall survival and disease-free survival at 5 years after the first anniversary post HCT was 78 and 74%, respectively. The most common causes of late mortality were disease relapse, chronic GVHD and infections. The major risk factors for late mortality included chronic GVHD requiring immunosuppression, being transplanted between 2005 and 2009 compared to later years and male sex. Patients with high risk disease risk index (DRI) had worse OS compared to low risk DRI. The risk factors for late relapse included male sex and high/very high disease risk index. The projected long-term survival of 1-year survivors following allogeneic HCT is excellent. However, some patients remain at high risk of late relapse and late mortality. Early referral to transplant, adopting post-transplant consolidation strategies for high risk patients, and implementing newer GVHD prevention methods are potential interventions to help minimize the risk of late relapse and death.
异基因造血细胞移植(HCT)尤其是在移植后的第一年,会伴有显著的发病率和死亡率。在本研究中,我们调查了异基因造血细胞移植后至少存活一年且无复发迹象患者的长期预后。我们分析了2005年至2016年间连续389例接受来自单倍体相合、单倍体不匹配或单倍体相同供者的异基因移植患者的记录,这些患者在移植后一年存活且无疾病。患者特征和预后参数从我们的机构数据库中提取,数据已前瞻性录入该数据库。共有389例患者符合选择标准,供者移植物包括单倍体相合37%、单倍体不匹配39%和单倍体相同亲属24%。从异基因造血细胞移植时起,幸存者的中位随访时间为48.2个月。异基因造血细胞移植一周年后5年的中位总生存率和无病生存率分别为78%和74%。晚期死亡的最常见原因是疾病复发、慢性移植物抗宿主病(GVHD)和感染。晚期死亡的主要危险因素包括需要免疫抑制的慢性GVHD、与后期年份相比在2005年至2009年间进行移植以及男性。疾病风险指数(DRI)高的患者与低风险DRI患者相比,总生存率更差。晚期复发的危险因素包括男性和高/极高疾病风险指数。异基因造血细胞移植后1年幸存者的预计长期生存率良好。然而,一些患者仍有较高的晚期复发和晚期死亡风险。早期转诊进行移植、对高危患者采用移植后巩固策略以及实施更新的GVHD预防方法是有助于降低晚期复发和死亡风险的潜在干预措施。