Clinical analysis on efficacy of rabbit anti-thymocyte globulin combined with cyclosporine in treatment of 128 children with aplastic anemia

Su Liu, Shaofen Lin, Qihui Chen, H. Xue, Hong-gui Xu, Shao-liang Huang, Chun Chen
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Abstract

Objective To evaluate efficacy, complications and influencing factors of children with aplastic anemia(AA)who were receiving rabbit anti-thymocyte globulin (rATG) combined with cyclosporine for immunosuppressive therapy (IST), and to explore optimal therapy for different clinical types of AA according to severity. Methods From 1st January 2006 to 1st February 2017, a total of 128 children who were diagnosed as AA by peripheral blood routine and bone marrow morphology and/or bone marrow pathology, and accepted rATG combined with cyclosporine in Department of Pediatric, Sun Yat-sen Memorial Hospital, Sun Yat-sen University. According to the clinical classification of the disease, the subjects were divided into non-severe aplastic anemia (NSAA) group (n=22), severe aplastic anemia (SAA) group (n=63), and very severe aplastic anemia (VSAA) group (n=43). The clinical data of the patients were retrospectively analyzed. The efficacy of the patients at 3, 6, 9 and 12 months after treatment and at the end of follow-up among 3 groups were evaluated by chi-square test. The treatment-related adverse reactions and prognosis were observed. Univariate analysis of different influencing factors, such as age, absolute value of neutrophils, platelet count, and reticulocyte were performed using the chi-square test. Statistically significant factors in the univariate analysis were included in the Cox proportional hazard regression model for multivariate analysis. Survival analysis was performed using the Kaplan-Meier method. The procedure of this study was accordance with the requirement of the revised World Medical Association Declaration of Helsinki in 2013. Informed consent was obtained from all guardians of participants. Results ① Of the 128 patients, 121 cases were evaluable, 5 cases were lost to follow-up, and 2 cases were early death. The complete remission (CR) rates at 3, 6, 9, and 12 months after treatment and at the end of follow-up were 5.0% (6/121), 14.9% (18/121), 16.5%(20/121), 28.9% (35/121) and 51.2% (62/121), respectively. The overall response rates were 33.9% (41/121), 38.9% (47/121), 49.6% (60/121), 62.8% (76/121) and 65.3% (79/121) , respectively. The response rates at 3 and 6 months after treatment in the NSAA group were 63.6% (14/22) and 68.2% (15/22), which were significantly higher than those of 30.5% (18/59) and 39.0% (23/59) in SAA group, 22.5% (9/40) and 22.5% (9/40) in VSAA group, the former were statistically different from the latter two (χ2=11.416, 13.297, P=0.001, 0.05). ④ The lymphocyte count 0.05). Conclusions The treatment of rATG combined with cyclosporine in children with SAA and VSAA has a higher response rate and a lower incidence of serious complications, which can be used as first-line treatment in the absence of appropriate donors. The lymphocyte count<1.5×109/L, platelet count≥20×109/L, and decreased CD3+ CD4+ cell ratio might be predictors of good response to rATG combined with cyclosporine in the treatment of children with AA. Key words: Anemia, aplastic; Immunosuppressive agents; Child; Rabbit anti-thymocyte globulin
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兔抗胸腺细胞球蛋白联合环孢素治疗儿童再生障碍性贫血128例临床分析
目的评价兔抗胸腺细胞球蛋白(rATG)联合环孢菌素免疫抑制治疗再生障碍性贫血(AA)患儿的疗效、并发症及影响因素,探讨不同临床类型再生障碍的最佳治疗方法。方法自2006年1月1日至2017年2月1日,在中山大学中山纪念医院儿科对128例经外周血常规、骨髓形态学和/或骨髓病理学诊断为AA的儿童进行rATG联合环孢菌素治疗。根据疾病的临床分型,受试者分为非重型再生障碍性贫血(NSAA)组(n=22)、重型再生障碍型贫血(SAA)组(n=63)和极重型再生障碍症贫血(VSAA)组(n=43)。对患者的临床资料进行回顾性分析。采用卡方检验对3组患者在治疗后3、6、9和12个月以及随访结束时的疗效进行评价。观察治疗相关的不良反应和预后。采用卡方检验对年龄、中性粒细胞绝对值、血小板计数和网织红细胞等不同影响因素进行单因素分析。将单变量分析中具有统计学意义的因素纳入Cox比例风险回归模型进行多变量分析。使用Kaplan-Meier方法进行生存分析。本研究的程序符合2013年修订的《赫尔辛基世界医学会宣言》的要求。获得了参与者所有监护人的知情同意。结果①128例患者中,可评价121例,失访5例,早期死亡2例。治疗后3、6、9和12个月以及随访结束时的完全缓解率分别为5.0%(6/121)、14.9%(18/121)、16.5%(20/121)、28.9%(35/121)和51.2%(62/121)。总有效率分别为33.9%(41/121)、38.9%(47/121)、49.6%(60/121)、62.8%(76/121)和65.3%(79/121)。NSAA组治疗后3个月和6个月的有效率分别为63.6%(14/22)和68.2%(15/22),显著高于SAA组的30.5%(18/59)和39.0%(23/59)、VSAA组的22.5%(9/40)和22.5%(9/20),④淋巴细胞计数0.05)。结论rATG联合环孢菌素治疗SAA和VSAA患儿有效率高,严重并发症发生率低,可作为缺乏合适供体的一线治疗方法。淋巴细胞计数<1.5×109/L,血小板计数≥20×109/L和CD3+CD4+细胞比例降低可能是rATG联合环孢菌素治疗AA患儿疗效良好的预测因素;免疫抑制剂;儿童;兔抗胸腺细胞球蛋白
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期刊介绍: The International Journal of Transfusion and Hematology was founded in September 1978. It is a comprehensive academic journal in the field of transfusion and hematology, supervised by the National Health Commission and co-sponsored by the Chinese Medical Association, West China Second Hospital of Sichuan University, and the Institute of Transfusion Medicine of the Chinese Academy of Medical Sciences. The journal is a comprehensive academic journal that combines the basic and clinical aspects of transfusion and hematology and is publicly distributed at home and abroad. The International Journal of Transfusion and Hematology mainly reports on the basic and clinical scientific research results and progress in the field of transfusion and hematology, new experiences, new methods, and new technologies in clinical diagnosis and treatment, introduces domestic and foreign research trends, conducts academic exchanges, and promotes the development of basic and clinical research in the field of transfusion and hematology.
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