Hagenbeek Anton, Gadeberg Ole, Johnson Peter, Pedersen Lars Møller, Walewski Jan, Hellmann Andrzej, Link Brian K, Robak Tadeusz, Wojtukiewicz Marek, Pfreundschuh Michael, Kneba Michael, Engert Andreas, Sonneveld Pieter, Flensburg Mimi, Petersen Jørgen, Losic Nedjad, Radford John
University Medical Center Utrecht, Department of Hematology, Utrecht, The Netherlands.
Blood. 2008 Jun 15;111(12):5486-95. doi: 10.1182/blood-2007-10-117671. Epub 2008 Apr 4.
Ofatumumab is a unique monoclonal antibody that targets a distinct small loop epitope on the CD20 molecule. Preclinical data show that ofatumumab is active against B-cell lymphoma/chronic lymphocytic leukemia cells with low CD20-antigen density and high expression of complement inhibitory molecules. In a phase 1/2 trial evaluating safety and efficacy of ofatumumab in relapsed or refractory follicular non-Hodgkin lymphoma (FL) grade 1 or 2, 4 dose groups of 10 patients received 4 weekly infusions of 300, 500, 700, or 1000 mg. Patients had a median of 2 prior FL therapies and 13% had elevated lactate dehydrogenase. No safety concerns or maximum tolerated dose was identified. A total of 274 adverse events were reported; 190 were judged related to ofatumumab, most occurring on the first infusion day with Common Terminology Criteria grade 1 or 2. Eight related events were grade 3. Treatment caused immediate and profound B-cell depletion, and 65% of patients reverted to negative BCL2 status. Clinical response rates ranged from 20% to 63%. Median time to progression for all patients/responders was 8.8/32.6 months, and median duration of response was 29.9 months at a median/maximum follow-up of 9.2/38.6 months. Ofatumumab is currently being evaluated in patients with rituximab-refractory FL. This trial was registered at www.clinicaltrials.gov as #NCT00092274.
奥法木单抗是一种独特的单克隆抗体,靶向CD20分子上一个独特的小环表位。临床前数据表明,奥法木单抗对CD20抗原密度低且补体抑制分子高表达的B细胞淋巴瘤/慢性淋巴细胞白血病细胞具有活性。在一项评估奥法木单抗治疗复发或难治性1或2级滤泡性非霍奇金淋巴瘤(FL)的安全性和疗效的1/2期试验中,4个剂量组各10名患者接受了4次每周一次的300、500、700或1000 mg输注。患者既往接受FL治疗的中位数为2次,13%的患者乳酸脱氢酶升高。未发现安全问题或最大耐受剂量。共报告了274例不良事件;190例被判定与奥法木单抗有关,大多数发生在首次输注当天,采用通用术语标准分级为1或2级。8例相关事件为3级。治疗导致立即且显著的B细胞耗竭,65%的患者BCL2状态恢复为阴性。临床缓解率为20%至63%。所有患者/缓解者的中位进展时间为8.8/32.6个月,中位随访时间为9.2/38.6个月时,中位缓解持续时间为29.9个月。目前正在对利妥昔单抗难治性FL患者进行奥法木单抗评估。该试验已在www.clinicaltrials.gov注册,编号为#NCT00092274。