Adis, a Wolters Kluwer Business, Auckland, New Zealand.
Drugs. 2010 May 28;70(8):1013-9. doi: 10.2165/11203850-000000000-00000.
Ofatumumab is a fully human anti-CD20 monoclonal antibody that induces antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity in CD20-expressing B lymphocytes. Ofatumumab is highly potent in lysing B cells, and this appears to stem from its binding site on the short extracellular loop of the target CD20 protein and its slow release from the target molecule. In a pivotal, noncomparative study in patients with fludarabine- and alemtuzumab-refractory chronic lymphocytic leukaemia (CLL), ofatumumab induced objective responses in 58% (99% CI 40, 74) of patients, which met a prespecified superiority criterion. The median duration of response was 7.1 months. The median progression-free survival was 5.7 months and the median overall survival was 13.7 months. In patients with fludarabine- and alemtuzumab-refractory CLL, infections and neutropenia were the most frequent treatment-related adverse events (all grades) that occurred during ofatumumab treatment; infections that commenced during treatment led to death in five patients (8%).
奥法妥木单抗是一种完全人源化抗 CD20 单克隆抗体,可诱导表达 CD20 的 B 淋巴细胞发生抗体依赖性细胞介导的细胞毒性和补体依赖性细胞毒性。奥法妥木单抗可高效裂解 B 细胞,这似乎源于其在靶 CD20 蛋白短细胞外环上的结合位点,以及其从靶分子上的缓慢释放。在一项关键性、非对照研究中,奥法妥木单抗治疗氟达拉滨和阿仑单抗难治性慢性淋巴细胞白血病(CLL)患者,58%(99%CI40,74)的患者获得了客观缓解,符合预先设定的优势标准。缓解的中位持续时间为 7.1 个月。中位无进展生存期为 5.7 个月,中位总生存期为 13.7 个月。在氟达拉滨和阿仑单抗难治性 CLL 患者中,感染和中性粒细胞减少是奥法妥木单抗治疗期间最常见的治疗相关不良事件(所有级别);5 名患者(8%)的治疗期间起始感染导致死亡。