Department of Biochemistry and Medical Biotechnologies, Federico II University of Naples, Italy.
Br J Haematol. 2010 Mar;148(5):791-6. doi: 10.1111/j.1365-2141.2009.08027.x. Epub 2009 Dec 7.
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.
一项以阿仑单抗为基础的实验性免疫抑制治疗(IST)方案在 35 例严重再生障碍性贫血(SAA)、纯红细胞再生障碍(PRCA)或纯白细胞减少性再生障碍(PWCA)患者中进行了研究。阿仑单抗总剂量为 73-103mg 皮下注射,随后给予环孢素。该方案未观察到与治疗相关的严重毒性。不良事件无临床相关性;感染事件罕见。SAA、PRCA 和 PWCA 的总反应率分别为 58%、84%和 100%,相应的 6 个月累积反应概率分别为 84%、84%和 100%。皮下注射阿仑单抗是一种可行且足够安全的 IST 方案,适用于患有免疫介导骨髓衰竭的患者。