[异基因造血干细胞移植治疗联合免疫缺陷症的疗效和预后分析]。

P. Wang, X. Qian, W. Jiang, H. Wang, J. Hou, J. Sun, X. C. Wang, X. Zhai
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引用次数: 0

摘要

目的评估异基因造血干细胞移植治疗联合免疫缺陷症(CID)的疗效,并探讨预后风险因素。方法:在这一回顾性队列研究中,研究人员对接受异体造血干细胞移植的患者进行了分析:在这项回顾性队列研究中,分析了2014年2月至2022年4月在复旦大学附属儿童医院接受异基因造血干细胞移植的73名CID患儿的临床特征、实验室检查和预后。根据疾病的亚型,所有患者被分为重症联合免疫缺陷病(SCID)组和其他CID组。根据供体类型,将所有患者分为配对同胞供体组、配对非亲缘供体组、非亲缘脐带血组和单倍体供体组。采用 Kaplan-Meier 法和 Log-Rank 检验分析生存数据。采用 Cox 回归分析预后因素。结果在73名患者中,男性61人(84%),女性12人(16%)。55例(75%)患者为SCID,18例(25%)患者为其他CID。供体来源包括 2 名(3%)配型成功的兄弟姐妹供体(MSD)、3 名(4%)配型成功的非亲属供体(MUD)、64 名(88%)非亲属脐带血供体(UCB)和 4 名(5%)单倍体供体。移植时的年龄为 10.7(5.9,27.5)个月,随访时间为 36.2(2.5,62.9)个月。73名CID患者的3年总存活率为(67±6)%。SCID患者(55例)与其他CID患者(18例)的3年总生存率无明显差异((64±7)% vs. (78±10)%,χ2=1.31,P=0.252)。而接受MSD或MUD(5例)、UCB(64例)和单倍体供体(4例)移植的患者的3年总生存率无明显差异(100% (66±6)% vs. (50±25) %,χ2=2.30,P=0.317)。Cox回归分析显示,脓毒症病史(HR=2.55,95%CI 1.05-6.20,P=0.039)和移植时低蛋白血症(HR=2.96,95%CI 1.14-7.68,P=0.026)是影响CID儿科患者异基因造血干细胞移植预后的独立危险因素。结论异基因造血干细胞移植是治疗CID的有效方法。脓毒症病史和移植时的低白蛋白血症是影响预后的危险因素。加强移植前的感染预防和营养干预可改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of efficacy and prognosis of allogeneic hematopoietic stem cell transplantation for the treatment of combined immunodeficiency].
Objective: To evaluate the efficacy of allogeneic hematopoietic stem cell transplantation for the treatment of combined immunodeficiency (CID) and explore prognostic risk factors. Methods: In this retrospective cohort study, clinical characteristics, laboratory tests and prognosis of 73 CID children who underwent allogeneic hematopoietic stem cell transplantation from February 2014 to April 2022 in the Children's Hospital of Fudan University were analyzed. Based on the subtypes of diseases, all patients were divided into severe combined immunodeficiency disease (SCID) group and other CID group. Based on the types of donors, all patients were divided into matched sibling donor group, matched unrelated donor group, unrelated cord blood group, and haploidentical donor group. Kaplan-Meier method and Log-Rank test were used to analyze the survival data. Cox regression was used to analyze prognostic factors. Results: Among the 73 patients, there were 61 (84%) males and 12 (16%) females. Fifty-five (75%) patients were SCID, and 18 (25%) patients were other CID. Donor source included 2 (3%) matched sibling donors (MSD), 3 (4%) matched unrelated donors (MUD), 64 (88%) unrelated cord blood (UCB), and 4 (5%) haploidentical donors. The age at transplant was 10.7 (5.9, 27.5) months, and the follow-up time was 36.2 (2.5, 62.9) months. The 3-year overall survival rate of 73 patients with CID was (67±6) %. No significant difference was found in the 3-year overall survival rates between patients with SCID (55 cases) and other CID (18 cases) ((64±7) % vs. (78±10) %, χ2=1.31, P=0.252). And no significant difference was found in the 3-year overall survival rates among patients who received MSD or MUD (5 cases), UCB (64 cases), and haploidentical donor (4 cases) transplant (100% (66±6)% vs. (50±25) %, χ2=2.30, P=0.317). Cox regression analysis showed that the medical history of sepsis (HR=2.55, 95%CI 1.05-6.20, P=0.039) and hypoalbuminemia at transplant (HR=2.96, 95%CI 1.14-7.68, P=0.026) were independent risk factors for the prognosis of allogeneic hematopoietic stem cell transplantation in pediatric patients with CID. Conclusions: Allogeneic hematopoietic stem cell transplantation is an effective treatment for CID. The medical history of sepsis and hypoalbuminemia at transplant were risk factors for prognosis. Enhancing infection prevention and nutritional intervention before transplant can improve patient prognosis.
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