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兔抗胸腺细胞球蛋白治疗重型再生障碍性贫血的疗效。

Efficacy of rabbit anti-thymocyte globulin in severe aplastic anemia.

机构信息

Department of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Haematologica. 2011 Sep;96(9):1269-75. doi: 10.3324/haematol.2011.042622. Epub 2011 May 23.

Abstract

BACKGROUND

A combination of horse anti-thymocyte globulin and cyclosporine produces responses in 60-70% of patients with severe aplastic anemia. We performed a phase II study of rabbit anti-thymocyte globulin and cyclosporine as first-line therapy for severe aplastic anemia.

DESIGN AND METHODS

Twenty patients with severe aplastic anemia treated with rabbit anti-thymocyte globulin were compared to 67 historical control cases with matched clinical characteristics treated with horse anti-thymocyte globulin.

RESULTS

Response rates at 3, 6 and 12 months were similar for patients treated with rabbit anti-thymocyte globulin or horse anti-thymocyte globulin: 40% versus 55% (P=0.43), 45% versus 58% (P=0.44) and 50% versus 58% (P=0.61), respectively. No differences in early mortality rates or overall survival were observed. We then performed multivariable analyses of response at 6 months and overall survival and identified the presence of a paroxysmal nocturnal hemoglobinuria clone (P=0.01) and a pretreatment absolute reticulocyte count greater than 30×10(9)/L (P=0.007) as independent predictors of response and younger age (P=0.003), higher pretreatment absolute neutrophil (P=0.02) and absolute lymphocyte counts (P=0.03) as independent predictors of overall survival. None of the immunogenetic polymorphisms studied was predictive of response to immunosupressive therapy.

CONCLUSIONS

Despite reports suggesting differences in biological activity of different anti-thymocyte globulin preparations, rabbit and horse anti-thymocyte globulin appear to have a similar efficacy for up-front treatment of severe aplastic anemia. Clinicaltrial.gov: NCT01231841).

摘要

背景

马抗胸腺细胞球蛋白和环孢素的联合治疗可使 60-70%的重型再生障碍性贫血患者产生反应。我们进行了一项兔抗胸腺细胞球蛋白和环孢素作为重型再生障碍性贫血一线治疗的 II 期研究。

设计和方法

将 20 例接受兔抗胸腺细胞球蛋白治疗的重型再生障碍性贫血患者与 67 例具有匹配临床特征的接受马抗胸腺细胞球蛋白治疗的历史对照病例进行比较。

结果

接受兔抗胸腺细胞球蛋白或马抗胸腺细胞球蛋白治疗的患者在 3、6 和 12 个月时的反应率相似:40%对 55%(P=0.43)、45%对 58%(P=0.44)和 50%对 58%(P=0.61)。未观察到早期死亡率或总生存率的差异。然后,我们对 6 个月时的反应和总生存率进行了多变量分析,并确定阵发性睡眠性血红蛋白尿克隆的存在(P=0.01)和治疗前绝对网织红细胞计数大于 30×10(9)/L(P=0.007)是反应和年龄较小(P=0.003)、治疗前绝对中性粒细胞(P=0.02)和绝对淋巴细胞计数较高(P=0.03)的独立预测因子。研究中没有任何免疫遗传多态性被预测为免疫抑制治疗的反应。

结论

尽管有报道称不同抗胸腺细胞球蛋白制剂的生物学活性存在差异,但兔抗胸腺细胞球蛋白和马抗胸腺细胞球蛋白在重型再生障碍性贫血的一线治疗中似乎具有相似的疗效。Clinicaltrial.gov:NCT01231841)。

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