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Successful therapy of chronic graft-versus-host disease manifesting as pure red cell aplasia with single-agent rituximab.

机译:单药利妥昔单抗可成功治疗表现为纯红细胞发育不良的慢性移植物抗宿主病。

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Recently, Zaja et al,described the G1TMO experience with rituximab as therapy for chronic graft-versus-host disease (cGVHD). In their series, an encouraging overall response rate of 65% was observed, particularly among patients with cutaneous cGVHD. One patient with cGVHD manifesting as a pure red cell aplasia (PRCA) failed to demonstrate response. Only one other report regarding the efficacy of rituximab for cGVHD manifesting as PRCA has been published to date; here, we report a patient with PRCA as a manifestation of cGVHD who was successfully treated with single-agent rituximab.
机译:最近,Zaja等人将利妥昔单抗的G1TMO经验描述为慢性移植物抗宿主病(cGVHD)的治疗方法。在他们的系列研究中,观察到令人鼓舞的总体缓解率为65%,尤其是在皮肤cGVHD患者中。一名表现为纯红细胞发育不良(PRCA)的cGVHD患者未能表现出应答。迄今为止,仅发表了另一篇有关利妥昔单抗治疗cGVHD表现为PRCA的功效的报告;在这里,我们报告了一位成功使用单药利妥昔单抗治疗的PRCA患者,其为cGVHD的表现。

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