University of California Medical Center, The Helen Diller Comprehensive Cancer Center, 400 Parnassus Ave, San Francisco, CA 94143-0324, USA.
J Clin Oncol. 2009 Dec 20;27(36):6101-8. doi: 10.1200/JCO.2009.22.2554. Epub 2009 Nov 16.
PURPOSE Mantle-cell lymphoma (MCL) is an aggressive B-cell non-Hodgkin's lymphoma with a poor prognosis. We explored the feasibility, safety, and effectiveness of an aggressive immunochemotherapy treatment program that included autologous stem-cell transplantation (ASCT) for patients up to age 69 years with newly diagnosed MCL. PATIENTS AND METHODS The primary end point was 2-year progression-free survival (PFS). A successful trial would yield a 2-year PFS of at least 50% and an event rate (early progression plus nonrelapse mortality) less than 20% at day +100 following ASCT. Seventy-eight patients were treated with two or three cycles of rituximab combined with methotrexate and augmented CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone). This treatment was followed by intensification with high doses of cytarabine and etoposide combined with rituximab and filgrastim to mobilize autologous peripheral-blood stem cells. Patients then received high doses of carmustine, etoposide, and cyclophosphamide followed by ASCT and two doses of rituximab. Results There were two nonrelapse mortalities, neither during ASCT. With a median follow-up of 4.7 years, the 2-year PFS was 76% (95% CI, 64% to 85%), and the 5-year PFS was 56% (95% CI, 43% to 68%). The 5-year overall survival was 64% (95% CI, 50% to 75%). The event rate by day +100 of ASCT was 5.1%. CONCLUSION The Cancer and Leukemia Group B 59909 regimen is feasible, safe, and effective in patients with newly diagnosed MCL. The incorporation of rituximab with aggressive chemotherapy and ASCT may be responsible for the encouraging outcomes demonstrated in this study, which produced results comparable to similar treatment regimens.
套细胞淋巴瘤(MCL)是一种侵袭性 B 细胞非霍奇金淋巴瘤,预后较差。我们探索了一种强化免疫化疗治疗方案的可行性、安全性和有效性,该方案包括自体干细胞移植(ASCT),适用于年龄不超过 69 岁的新诊断 MCL 患者。
主要终点是 2 年无进展生存率(PFS)。如果在 ASCT 后第 100 天,2 年 PFS 至少为 50%,事件率(早期进展加上非复发死亡率)小于 20%,则试验成功。78 例患者接受了两到三个周期的利妥昔单抗联合甲氨蝶呤和改良 CHOP(环磷酰胺、多柔比星、长春新碱和泼尼松)治疗。随后,采用高剂量阿糖胞苷和依托泊苷联合利妥昔单抗和非格司亭强化治疗,动员自体外周血干细胞。然后,患者接受卡莫司汀、依托泊苷和环磷酰胺高剂量治疗,继之以 ASCT 和两剂利妥昔单抗。
有 2 例非复发死亡,但均不在 ASCT 期间。中位随访 4.7 年后,2 年 PFS 为 76%(95%CI,64%至 85%),5 年 PFS 为 56%(95%CI,43%至 68%)。5 年总生存率为 64%(95%CI,50%至 75%)。ASCT 后第 100 天的事件发生率为 5.1%。
癌症和白血病组 B59909 方案在新诊断的 MCL 患者中是可行的、安全的、有效的。利妥昔单抗联合强化化疗和 ASCT 的应用可能是该研究中令人鼓舞结果的原因,该结果与类似的治疗方案相当。