Department of Medicine, Division of Hematology and Oncology, Long Island Jewish Medical Center, CLL Research and Treatment Center, New Hyde Park, NY, USA,
Med Oncol. 2011 Jun;28(2):532-8. doi: 10.1007/s12032-010-9478-3. Epub 2010 Mar 17.
This prospective, single-arm study utilized alemtuzumab as a single agent in a novel maintenance schedule in previously treated chronic lymphocytic leukemia patients with the goal of delaying progression of disease and requirement for chemotherapy. In previously treated CLL patients who had achieved stable disease or better, the following schedule of subcutaneous alemtuzumab was administered: a dose escalation in the first week (3, 10 and 30 mg), followed by 7 weeks of 30 mg alemtuzumab once weekly, 16 weeks of 30 mg once every 2 weeks, followed by once every 3 weeks for 24 weeks. Thus, the entire duration of the planned treatment was 48 weeks. A total of 12 patients were enrolled 11 of which had at least one marker of poor prognosis (unmutated, Zap 70+, CD38+, del11q and del17p). The median chemotherapy-free interval was 13 months, and the median time to disease progression was 10 months. Three patients achieved a CR, one achieved nPR, one had a PR, five failed and two had shown a beneficial response but because of recurrent ITP had to stop alemtuzumab. In six of the 10 patients with previously relapsed disease, the chemotherapy-free interval was longer than their prior chemotherapy-free period. One patient had a reactivation of CMV antigenemia, and another had a bacterial pneumonia. There were no grade 3 or 4 toxicities. Alemtuzumab used in a maintenance schedule is a potentially safe and useful tool in delaying disease progression and chemotherapy-free intervals in previously treated CLL patients.
这项前瞻性、单臂研究在先前接受治疗的慢性淋巴细胞白血病患者中使用阿仑单抗作为单一药物,并采用新的维持方案,目的是延缓疾病进展和化疗的需求。在先前接受治疗的 CLL 患者中,疾病达到稳定或更好的患者,接受以下皮下阿仑单抗的治疗方案:第 1 周进行剂量递增(3、10 和 30mg),然后每周给予 7 周 30mg 阿仑单抗,每 2 周给予 16 周 30mg 阿仑单抗,然后每 3 周给予 24 周 30mg 阿仑单抗。因此,计划治疗的总持续时间为 48 周。共招募了 12 名患者,其中 11 名患者至少有一个不良预后标志物(未突变、Zap 70+、CD38+、del11q 和 del17p)。无化疗间隔的中位数为 13 个月,疾病进展的中位数时间为 10 个月。3 名患者达到完全缓解,1 名患者达到接近完全缓解,1 名患者达到部分缓解,5 名患者失败,2 名患者出现获益反应,但由于 ITP 复发,不得不停止阿仑单抗治疗。在先前复发疾病的 10 名患者中,有 6 名患者的无化疗间隔时间长于其先前的无化疗期。1 名患者出现 CMV 抗原血症再激活,另 1 名患者发生细菌性肺炎。没有 3 级或 4 级毒性。在先前接受治疗的 CLL 患者中,采用维持方案使用阿仑单抗是一种潜在安全且有用的工具,可以延缓疾病进展和无化疗间隔。