Comparison of two dosages of rabbit antithymocyte globulin (r-ATG) in treating children with severe aplastic anemia.

Comparison of two dosages of rabbit antithymocyte globulin (r-ATG) in treating children with severe aplastic anemia.
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DOI:
10.1691/ph.2018.7353
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发表时间:
2018-05
期刊:
Die Pharmazie
影响因子:
--
通讯作者:
Shaofen Lin;Su Liu;H. Xue;Junbin Huang;Jian Wang;Qihui Chen;Bihong Zhang;Chun Chen
Shaofen Lin;Su Liu;H. Xue;Junbin Huang;Jian Wang;Qihui Chen;Bihong Zhang;Chun Chen
中科院分区:
其他
文献类型:
--
作者:
Shaofen Lin;Su Liu;H. Xue;Junbin Huang;Jian Wang;Qihui Chen;Bihong Zhang;Chun Chen

文献摘要

相似文献

本研究比较了两种不同剂量兔抗胸腺细胞球蛋白(r-ATG)联合环孢素(CsA)治疗儿童严重再生性贫血(SAA)的疗效和安全性。回顾性分析2005年1月至2017年1月中山大学中山纪念医院122例SAA患儿行r-ATG/CsA的临床资料。55例r-ATG剂量为2.5mg/(kg·d,组1),67例r-ATG剂量为3.5 mg/(kg·d,组2),连续给药5 d。治疗后第3、6个月,组2有效率高于组1 (45.5% vs 26.4%, P=0.032; 54.5% vs 35.8%, P=0.042)。治疗后第9、12个月,两组有效率相近(71.2% vs 54.9%, P=0.077; 75.9% vs 68.6%, P=0.399)。两组血清疾病发生率(74.5% vs 79.1%, P=0.551)、短期感染率(76.4% vs 62.7%, P=0.105)、早期死亡率(3.6% vs 1.5%, P=0.447)、3年总生存率(89.5% vs 90.1%, P=0.932)差异均无统计学意义。r-ATG/CSA治疗SAA安全有效。两种r-ATG剂量的最终疗效和安全性相同。但本研究随访时间较短,需进一步随访组间远期并发症及生存率的比较。
In this study, efficacy and safety of two different dosages of rabbit antithymocyte globulin (r-ATG) combined with cyclosporine (CsA) in treating children with severe aplastic anemia (SAA) were compared. The clinical data of 122 SAA children treated by r-ATG/CsA between Jan 2005 and Jan 2017 at Sun Yat-sen Memorial Hospital of Sun Yat-sen University were retrospectively analyzed. The r-ATG dose of 55 cases was 2.5mg/(kg·d, group 1), and in the other 67 cases it was 3.5 mg/(kg·d, group 2). r-ATG was continuously administered for 5 days. In the 3rd and 6th month after treatment, the efficacy rate of group 2 was higher than that of group 1 (45.5% vs 26.4%, P=0.032; 54.5% vs 35.8%, P=0.042). In the 9th and 12th month after treatment, the efficacy rates of both groups were similar (71.2% vs 54.9%, P=0.077; 75.9% vs 68.6%, P=0.399). The incidence rates of serum diseases (74.5% vs 79.1%, P=0.551), short-term infection rates (76.4% vs 62.7%, P=0.105), early mortality (3.6% vs 1.5%, P=0.447), and 3-year overall survival rates (89.5% vs 90.1%, P=0.932) of both groups showed no significant differences. The r-ATG/CSA therapy was safe and effective towards SAA. The final efficacies and safety of the two r-ATG dosages were equal. However, the follow-up period in this study was relatively short, so the intergroup comparison of the long-term complications and survival rates needed to be further followed up.