Department of Hematology, Medical University of Lodz, Ciolkowskiego 2, Lodz, Poland 93-510.
J Clin Oncol. 2010 Apr 1;28(10):1756-65. doi: 10.1200/JCO.2009.26.4556. Epub 2010 Mar 1.
PURPOSE: Rituximab, a monoclonal antibody that targets the CD20 cell surface antigen, has clinical activity in patients with non-Hodgkin's lymphoma and other B-lymphocyte disorders when administered alone or in combination with chemotherapy. Promising results have previously been reported in nonrandomized studies in patients with chronic lymphocytic leukemia (CLL). This trial was designed to compare chemoimmunotherapy with chemotherapy alone in patients with previously treated CLL. PATIENTS AND METHODS: This international, multicenter, randomized trial compared six cycles of rituximab plus fludarabine and cyclophosphamide (R-FC) with six cycles of fludarabine and cyclophosphamide alone (FC) in patients with previously treated CLL. A total of 552 patients with Binet stage A (1%), B (59%), or C (31%) disease entered the study and were randomly assigned to receive R-FC (n = 276) or FC (n = 276). RESULTS: After a median follow-up time of 25 months, rituximab significantly improved progression-free survival in patients with previously treated CLL (hazard ratio = 0.65; P < .001; median, 30.6 months for R-FC v 20.6 months for FC). Event-free survival, response rate, complete response rate, duration of response, and time to new CLL treatment or death were also significantly improved. Although the rates of adverse events, grade 3 or 4 events, and serious adverse events were slightly higher in the R-FC arm, R-FC was generally well tolerated, with no new safety findings and no detrimental effect on quality of life. CONCLUSION: R-FC significantly improved the outcome of patients with previously treated CLL.
目的:利妥昔单抗是一种针对 CD20 细胞表面抗原的单克隆抗体,单独使用或与化疗联合使用时,在非霍奇金淋巴瘤和其他 B 淋巴细胞疾病患者中具有临床活性。先前在慢性淋巴细胞白血病(CLL)患者的非随机研究中已经报告了有希望的结果。本试验旨在比较先前治疗过的 CLL 患者的化疗免疫治疗与单独化疗。
患者和方法:这项国际、多中心、随机试验比较了利妥昔单抗联合氟达拉滨和环磷酰胺(R-FC)与氟达拉滨和环磷酰胺单独(FC)治疗 6 个周期在先前治疗过的 CLL 患者中的疗效。共有 552 名 Binet 分期为 A(1%)、B(59%)或 C(31%)的患者进入研究,并随机分为接受 R-FC(n=276)或 FC(n=276)组。
结果:中位随访时间为 25 个月后,利妥昔单抗显著改善了先前治疗的 CLL 患者的无进展生存期(风险比=0.65;P<0.001;中位 R-FC 为 30.6 个月,FC 为 20.6 个月)。无事件生存、反应率、完全反应率、反应持续时间以及新 CLL 治疗或死亡的时间也显著改善。尽管 R-FC 组的不良事件、3 或 4 级事件和严重不良事件发生率略高,但 R-FC 总体耐受性良好,无新的安全性发现,对生活质量也没有不利影响。
结论:R-FC 显著改善了先前治疗的 CLL 患者的预后。
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