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Alemtuzumab is safe and effective as immunosuppressive treatment for aplastic anaemia and single-lineage marrow failure: a pilot study and a survey from the EBMT WPSAA

机译:Alemtuzumab作为再生障碍性贫血和单系骨髓衰竭的免疫抑制剂治疗是安全有效的:EBMT WPSAA的一项试点研究和一项调查

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摘要

An alemtuzumab-based experimental immunosuppressive treatment (IST) regimen was investigated in 35 patients with severe aplastic anaemia (SAA), pure red cell (PRCA) or pure white cell aplasia (PWCA). Alemtuzumab total dose was 73-103 mg s.c., followed by cyclosporine. No serious toxicity due to the regimen was observed. Adverse events were clinically irrelevant; infectious events were rare. The total response rate was 58%, 84% and 100% in SAA, PRCA and PWCA, respectively, with corresponding 6 months cumulative response probabilities of 84%, 84% and 100%. Subcutaneous alemtuzumab is a feasible and sufficiently safe IST regimen for patients suffering from immune-mediated marrow failures.
机译:在35名重度再生障碍性贫血(SAA),纯红细胞(PRCA)或纯白细胞发育不全(PWCA)的患者中研究了基于阿仑单抗的实验性免疫抑制治疗(IST)方案。 Alemtuzumab的总剂量为73-103 mg s.c.,然后是环孢霉素。由于该方案未观察到严重的毒性。不良事件在临床上无关紧要;传染事件很少见。 SAA,PRCA和PWCA的总缓解率分别为58%,84%和100%,相应的6个月累积缓解率分别为84%,84%和100%。对于患有免疫介导的骨髓衰竭的患者,皮下阿仑单抗是一种可行且足够安全的IST方案。

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