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首页> 外文期刊>Annals of hematology >Comparison between horse and rabbit antithymocyte globulin as first-line treatment for patients with severe aplastic anemia: a single-center retrospective study.
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Comparison between horse and rabbit antithymocyte globulin as first-line treatment for patients with severe aplastic anemia: a single-center retrospective study.

机译:严重再生障碍性贫血一线治疗中马和兔抗胸腺细胞球蛋白的比较:单中心回顾性研究。

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摘要

The best antithymocyte globulin preparation for first-line immune suppression in patients with severe aplastic anemia is still not clear. The aim of this study was to compare hematological response and overall survival in patients submitted to horse or rabbit antithymocyte globulin as first-line treatment for severe aplastic anemia. We retrospectively compared 71 consecutive patients with severe aplastic anemia, classified according to the antithymocyte globulin preparation. Analyses included variables related to patients and to immune suppression. Forty two patients (59.1%) received horse and 29 (40.9%) rabbit antithymocyte globulin. Response rates were higher at 6 months in patients submitted to horse in comparison to rabbit antithymocyte globulin (59.5% versus 34.5% respectively, p = 0.05). Median time to response was similar between the two groups (99 versus 88.5 days, respectively, for horse and rabbit antithymocyte globulin; p = 0.98). Overall survival at 2 years was significantly higher in patients submitted to horse in comparison to rabbit antithymocyte globulin (78.4% versus 55.4%, p = 0.03). Post-treatment response was strongly associated with survival at 2 years (97% in responders versus 41.2% in non-responders, p < 0.001). Use of rabbit antithymocyte globulin was an independent predictor of death (odds ratio 2.5; 95% confidence interval 1.03-6.04; p = 0.04). Rabbit antithymocyte globulin was associated with a significant and prolonged lymphopenia in comparison with horse antithymocyte globulin. Our data suggest the superiority of horse over rabbit antithymocyte globulin as first-line treatment for severe aplastic anemia, both regarding hematological response and survival.
机译:对于重生再生障碍性贫血的患者,一线免疫抑制的最佳抗胸腺细胞球蛋白制剂尚​​不清楚。本研究的目的是比较作为严重再生障碍性贫血一线治疗药物的马或兔抗胸腺细胞球蛋白患者的血液学反应和总体生存率。我们回顾性比较了71例重度再生障碍性贫血患者,根据抗胸腺细胞球蛋白制剂分类。分析包括与患者和免疫抑制有关的变量。四十二名患者(59.1%)接受了马匹治疗,而二十九名患者(40.9%)接受了兔抗胸腺细胞球蛋白治疗。与兔抗胸腺细胞球蛋白相比,接受马治疗的患者在6个月时的缓解率更高(分别为59.5%和34.5%,p = 0.05)。两组之间的中位反应时间相似(马和兔抗胸腺细胞球蛋白分别为99天和88.5天; p = 0.98)。与兔抗胸腺细胞球蛋白相比,接受马治疗的患者2年总生存率明显更高(78.4%对55.4%,p = 0.03)。治疗后反应与2年生存率密切相关(有反应者为97%,无反应者为41.2%,p <0.001)。兔抗胸腺细胞球蛋白的使用是死亡的独立预测因子(赔率2.5; 95%置信区间1.03-6.04; p = 0.04)。与马抗胸腺细胞球蛋白相比,兔抗胸腺细胞球蛋白与显着且延长的淋巴细胞减少有关。我们的数据表明,在血液学反应和生存方面,马均优于兔抗胸腺细胞球蛋白作为严重再生障碍性贫血的一线治疗。

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