首页> 外文期刊>The annals of pharmacotherapy >Ofatumumab: a novel anti-CD20 monoclonal antibody for treatment of refractory chronic lymphocytic leukemia.
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Ofatumumab: a novel anti-CD20 monoclonal antibody for treatment of refractory chronic lymphocytic leukemia.

机译:Ofatumumab:一种新型的抗CD20单克隆抗体,用于治疗难治性慢性淋巴细胞性白血病。

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摘要

OBJECTIVE: To present the current clinical evidence on ofatumumab for use in refractory chronic lymphocytic leukemia (CLL). DATA SOURCES: A literature search was performed using MEDLINE and PubMed (both 1966-May 2011), as well as the American Society of Hematology abstracts (2000-May 2011), using the primary search terms ofatumumab and HuMax-CD20. STUDY SELECTION AND DATA EXTRACTION: Clinical studies and abstracts available in the English language, describing the pharmacology, pharmacokinetics, clinical activity, and safety of ofatumumab in CLL were included in this review. DATA SYNTHESIS: Ofatumumab is a human immunoglobulin monoclonal antibody that binds to B-lymphocytes expressing CD-20 cell surface antigens. Ofatumumab was granted accelerated approval by the Food and Drug Administration in October 2009 for the treatment of CLL refractory to fludarabine and alemtuzumab. A Phase 1/2 trial has established the safety and tolerability of single-agent ofatumumab at an initial dose of 300 mg intravenously on week 1, followed by 2000 mg once weekly for 7 doses (weeks 2-8), followed by 2000 mg once every 4 weeks for 4 doses (weeks 9-12), for a total of 12 doses. The final analysis of a pivotal international multicenter trial has shown promising activity in patients with CLL refractory to fludarabine and alemtuzumab, demonstrating overall response rates of 44-51%, with prolonged progression-free and overall survival. Ofatumumab activity has also been shown in a variety of other malignant and nonmalignant conditions, including non-Hodgkin lymphoma, rheumatoid arthritis, and multiple sclerosis. The most common adverse effect is grade 1 and 2 infusion reactions. Other adverse effects include infection, neutropenia, anemia, rash, fever, and diarrhea. CONCLUSIONS: Clinical evidence suggests that ofatumumab is an effective agent in patients with CLL refractory to fludarabine and alemtuzumab. Data are awaited comparing ofatumumab to other salvage regimens. Until results of head-to-head trials are conducted comparing ofatumumab to existing regimens, it cannot be said whether ofatumumab is more efficacious or tolerable than currently available therapies.
机译:目的:介绍ofatumumab用于难治性慢性淋巴细胞白血病(CLL)的当前临床证据。数据来源:文献检索使用MEDLINE和PubMed(1966年-2011年5月),以及美国血液学摘要(2000年5月-2011年5月),使用atumumab和HuMax-CD20作为主要检索词。研究的选择和数据提取:本临床评价包括英文版的临床研究和摘要,描述了CLL中ofatumumab的药理学,药代动力学,临床活性和安全性。数据合成:Ofatumumab是一种人免疫球蛋白单克隆抗体,可与表达CD-20细胞表面抗原的B淋巴细胞结合。 Ofatumumab在2009年10月获得美国食品药品管理局的加速批准,用于治疗氟达拉滨和alemtuzumab难治性CLL。 1/2期临床试验建立了单剂量ofatumumab的安全性和耐受性,第1周静脉内初始剂量为300 mg,随后每周7次(2000-8周)每周一次2000 mg,随后为2000 mg一次每4周服用4剂(9-12周),共12剂。一项关键的国际多中心试验的最终分析显示,氟达拉滨和阿仑单抗对难治性CLL患者具有良好的活性,表明总缓解率为44-51%,无进展生存期和总生存期均延长。在许多其他恶性和非恶性疾病中,包括非霍奇金淋巴瘤,类风湿性关节炎和多发性硬化症,也显示了Ofatumumab的活性。最常见的不良反应是1级和2级输注反应。其他不良影响包括感染,中性粒细胞减少,贫血,皮疹,发烧和腹泻。结论:临床证据表明ofatumumab是氟达拉滨和阿仑单抗难治性CLL患者的有效药物。等待数据将ofatumumab与其他挽救方案进行比较。直到进行了ofatumumab与现有方案的比较的头对头试验结果之前,尚不能说ofatumumab是否比目前可用的疗法更有效或更可耐受。

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