[Clinical Analysis of Post-Transplant Lymphoproliferative Disorder after Hematopoietic Stem Cell Transplantation in Severe Aplastic Anemia Patients].

Hong-Min Yan, Xiao-Li Zheng, Ling Zhu, Li Ding, Dong-Mei Han, Jing Liu, Mei Xue, Sheng Li, Heng-Xiang Wang
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引用次数: 1

Abstract

Objective: To analyze the clinical characteristics of SAA patients with post-transplantation lymphoproliferative disease (PTLD) after allogeneic hematopoietic stem cell transplantation, and to improve diagnosis and treatment of PTLD.

Methods: The clinical data of 192 patients with SAA patients who underwent HSCT in a single center from September 2010 to September 2017 were analyzed retrospectively. All patients were received antithymocyte globulin(ATG) conditioning regimen and mesenchymal stem cell(MSC) infusion.

Results: Among 192 cases, PTLD occurred in 14 cases, the incidence was 7.29%, 9 of them were diagnosed by pathology, and 5 were diagnosed clinically. EBV infection occurred with a median time of 72(35-168) days, Viral load higher than 1×104 copies/ml occured in all PTLD patients. The incidence of probable PTLD in patients ≤12 years old and >12 years old was 11.11%, 2.38%, respectively (P<0.01). Univariate and multivariate analysis that the EBV infection, patients age≤12 years old, HLA-mismatch in URD-HSCT, grade II to IV aGVHD were the independent risk factors for PTLD. All PTLD patients were treated with rituximab(RTX) when EBV-DNA load higher than 1×104 copies/ml, or reducted the use of immunosuppression(RIS), patients with poor therapeutic effect were treated combined with EBV-specific CTLs(EBV-CTL) and chemotherapy. All patients were treated effectively, and the total effective rate was 100%. The median follow-up time was 65(62-115) months, and the overall survival rate was 92.85%. One patients died of cerebral hemorrhage, 7 months after PTLD curred.

Conclusion: The incidence of PTLD after HSCT with SAA who used ATG and MSC in conditioning regimen closely relates to EBV infection, age of patients≤12 years, HLA-mismatch in URD-HSCT, grade II to IV GVHD. Rituximab combined with RIS may reduce the incidence of PTLD, combined EBV-CTL and chemotherapy may be the useful and most important treatment for PTLD.

[严重再生障碍性贫血患者造血干细胞移植后淋巴细胞增生性疾病的临床分析]。
目的:分析同种异体造血干细胞移植后SAA合并移植后淋巴细胞增生性疾病(PTLD)的临床特点,提高对PTLD的诊断和治疗水平。方法:回顾性分析2010年9月至2017年9月在单中心接受HSCT治疗的192例SAA患者的临床资料。所有患者均接受抗胸腺细胞球蛋白(ATG)调理方案和间充质干细胞(MSC)输注。结果:192例患者中,PTLD发生14例,发病率为7.29%,其中病理确诊9例,临床确诊5例。EBV感染发生的中位时间为72(35-168)天,所有PTLD患者的病毒载量均高于1×104拷贝/ml。≤12岁和>12岁患者可能发生PTLD的发生率分别为11.11%和2.38% (P4拷贝/ml),或减少使用免疫抑制(RIS),治疗效果较差的患者联合ebv特异性ctl (EBV-CTL)和化疗。所有患者均得到有效治疗,总有效率为100%。中位随访时间65(62 ~ 115)个月,总生存率92.85%。1例患者在PTLD治愈后7个月死于脑出血。结论:采用ATG + MSC治疗方案的SAA HSCT术后PTLD的发生率与EBV感染、患者年龄≤12岁、URD-HSCT hla配错、II级至IV级GVHD密切相关。利妥昔单抗联合RIS可降低PTLD的发生率,EBV-CTL联合化疗可能是PTLD有效且最重要的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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