依库珠单抗治疗化疗引起的血栓性微血管病。

Clinical Nephrology. Case Studies Pub Date : 2020-04-17 eCollection Date: 2020-01-01 DOI:10.5414/CNCS109836
Lena Schulte-Kemna, Barbara Reister, Lucas Bettac, Ulla Ludwig, Daniel Fürst, Joannis Mytilineos, Carsten Bergmann, Rene van Erp, Bernd Schröppel
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摘要

血栓性微血管病(TMA)是一种罕见但严重的肿瘤及其化疗并发症。我们报告了两名化疗诱发 TMA 的患者,他们接受了短程末端补体抑制剂 eculizumab 的成功治疗。两名患者的微血管病性溶血性贫血很快得到缓解,肾功能也得到恢复。停用依库珠单抗后,在分别长达 47 个月和 15 个月的观察期内,病情均稳定缓解。我们的数据表明,依库珠单抗能有效治疗化疗引起的TMA。一旦补体激活条件得到控制,诱因消除,停用依库珠单抗是可行的。其他研究需要确定补体导向疗法的最佳持续时间,并验证停用此类疗法后的有效监测策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Eculizumab in chemotherapy-induced thrombotic microangiopathy.

Thrombotic microangiopathy (TMA) is a rare but severe complication of tumors and their chemotherapeutic treatment. We report on two patients with chemotherapy-induced TMA who were successfully treated with a short course of the terminal complement inhibitor eculizumab. Both patients quickly achieved remission of microangiopathic hemolytic anemia and recovery of renal function. After withdrawal of eculizumab, remission was stable over an observation period of 47 months and 15 months, respectively. Our data show that eculizumab is effective in treating chemotherapy-induced TMA. Discontinuation of eculizumab is feasible once the complement-activating condition is controlled and the trigger is eliminated. Additional studies need to determine the optimal duration of complement-directed therapies and validate effective monitoring strategies after discontinuation of such therapy.

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