Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA 02115, USA.
Blood. 2012 Mar 1;119(9):2093-9. doi: 10.1182/blood-2011-07-369629. Epub 2012 Jan 10.
Few randomized trials have compared therapies in mantle cell lymphoma (MCL), and the role of aggressive induction is unclear. The National Comprehensive Cancer Network (NCCN) Non-Hodgkin Lymphoma (NHL) Database, a prospective cohort study collecting clinical, treatment, and outcome data at 7 NCCN centers, provides a unique opportunity to compare the effectiveness of initial therapies in MCL. Patients younger than 65 diagnosed between 2000 and 2008 were included if they received RHCVAD (rituximab fractionated cyclophosphamide, vincristine, adriamycin, and dexamethasone), RCHOP+HDT/ASCR (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone + high-dose therapy/autologous stem cell rescue), RHCVAD+HDT/ASCR, or RCHOP. Clinical parameters were similar for patients treated with RHCVAD (n = 83, 50%), RCHOP+HDT/ASCR (n = 34, 20%), RCHOP (n = 29, 17%), or RHCVAD+HDT/ASCR (n = 21, 13%). Overall, 70 (42%) of the 167 patients progressed and 25 (15%) expired with a median follow-up of 33 months. There was no difference in progression-free survival (PFS) between aggressive regimens (P > .57), which all demonstrated superior PFS compared with RCHOP (P < .004). There was no difference in overall survival (OS) between the RHCVAD and RCHOP+HDT/ASCR (P = .98). RCHOP was inferior to RHCVAD and RCHOP+HDT/ASCR, which had similar PFS and OS. Despite aggressive regimens, the median PFS was 3 to 4 years. Future trials should focus on novel agents rather than comparing current approaches.
在套细胞淋巴瘤(MCL)中,很少有随机试验比较治疗方法,强化诱导的作用也不清楚。国家综合癌症网络(NCCN)非霍奇金淋巴瘤(NHL)数据库是一项前瞻性队列研究,在 NCCN 的 7 个中心收集临床、治疗和结局数据,为比较 MCL 初始治疗方法的有效性提供了独特的机会。纳入标准为 2000 年至 2008 年间诊断为年龄小于 65 岁的患者,接受过 RHCVAD(利妥昔单抗联合环磷酰胺、长春新碱、阿霉素和地塞米松)、RCHOP+HDT/ASCR(利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松+大剂量化疗/自体干细胞挽救)、RHCVAD+HDT/ASCR 或 RCHOP 治疗。接受 RHCVAD(n = 83,50%)、RCHOP+HDT/ASCR(n = 34,20%)、RCHOP(n = 29,17%)或 RHCVAD+HDT/ASCR(n = 21,13%)治疗的患者的临床参数相似。总的来说,167 例患者中 70 例(42%)进展,25 例(15%)死亡,中位随访 33 个月。强化方案之间的无进展生存(PFS)无差异(P >.57),与 RCHOP 相比,所有强化方案均显示出更好的 PFS(P <.004)。RHCVAD 和 RCHOP+HDT/ASCR 之间的总生存(OS)无差异(P =.98)。RCHOP 劣于 RHCVAD 和 RCHOP+HDT/ASCR,后两者的 PFS 和 OS 相似。尽管采用了强化方案,但中位 PFS 仍为 3 至 4 年。未来的试验应关注新型药物,而不是比较现有方法。