Yan Hong-Min, Zheng Xiao-Li, Zhu Ling, Ding Li, Han Dong-Mei, Liu Jing, Xue Mei, Li Sheng, Wang Heng-Xiang
Department of Hematology, The General Hospital of Air Force, Beijing 100142, China.
Department of Hematology, The General Hospital of Air Force, Beijing 100142, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022 Aug;30(4):1224-1229. doi: 10.19746/j.cnki.issn.1009-2137.2022.04.040.
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.
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.
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 1×10 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 1×10 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.
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.
分析接受异基因造血干细胞移植的重型再生障碍性贫血(SAA)患者发生移植后淋巴细胞增殖性疾病(PTLD)的临床特征,以提高PTLD的诊疗水平。
回顾性分析2010年9月至2017年9月在单中心接受造血干细胞移植(HSCT)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)预处理方案及间充质干细胞(MSC)输注。
192例患者中,14例发生PTLD,发生率为7.29%,其中9例经病理诊断,5例经临床诊断。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1×10拷贝/ml。≤12岁和>12岁患者中可能发生PTLD的发生率分别为11.11%、2.38%(P<0.01)。单因素和多因素分析显示,EBV感染、患者年龄≤12岁、非血缘脐血造血干细胞移植(URD - HSCT)中的HLA配型不合、Ⅱ至Ⅳ度急性移植物抗宿主病(aGVHD)是PTLD的独立危险因素。当EBV - DNA载量高于1×10拷贝/ml时,所有PTLD患者均接受利妥昔单抗(RTX)治疗,或减少免疫抑制剂的使用(RIS),治疗效果不佳的患者联合EBV特异性细胞毒性T淋巴细胞(EBV - CTL)及化疗。所有患者均治疗有效,总有效率为100%。中位随访时间为65(62 - 115)个月,总生存率为92.85%。1例患者在PTLD治愈后7个月死于脑出血。
采用ATG和MSC预处理方案的SAA患者HSCT后PTLD的发生率与EBV感染、患者年龄≤12岁、URD - HSCT中的HLA配型不合、Ⅱ至Ⅳ度移植物抗宿主病密切相关。利妥昔单抗联合RIS可能降低PTLD的发生率,联合EBV - CTL及化疗可能是PTLD有效且重要的治疗方法。