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原发性治疗联合方案及维持用利妥昔单抗治疗巨球蛋白血症的反应和生存情况。

Response and survival for primary therapy combination regimens and maintenance rituximab in Waldenström macroglobulinaemia.

机构信息

Bing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Br J Haematol. 2018 Apr;181(1):77-85. doi: 10.1111/bjh.15148. Epub 2018 Feb 22.

Abstract

Waldenström macroglobulinaemia (WM) is a rare and incurable lymphoma. Comparative studies evaluating the efficacy of primary therapy in symptomatic WM patients have not been performed. In this study, we compared response and survival outcomes in WM patients who received primary therapy with cyclophosphamide-dexamethasone-rituximab (CDR), bortezomib-dexamethasone-rituximab (BDR) and bendamustine-rituximab (Benda-R), as well as maintenance rituximab following primary therapy. Analyses were adjusted for relevant clinical factors associated with response and survival. Maintenance rituximab was analysed as a time-varying covariate. Our study included 182 patients, of which 57 (31%) received Benda-R, 87 (48%) BDR and 38 (21%) CDR; 116 (64%) received maintenance rituximab. The median time to best response was shorter for Benda-R and BDR than CDR (18, 20 and 30 months, respectively). Benda-R and BDR were associated with better median progression-free survival (PFS) than CDR (5·5, 5·8 and 4·8 years, respectively), and better 10-year overall survival rates (OS; 95%, 96% and 81%, respectively). Maintenance rituximab was associated with higher rates of major response (97% vs. 68%), and better median PFS (6·8 years vs. 2·8 years) and 10-year OS rate (84% vs. 66%) when compared to not receiving maintenance. Benda-R, BDR and maintenance rituximab associate with higher response rates and longer survival in WM patients than CDR and no maintenance, respectively.

摘要

华氏巨球蛋白血症(WM)是一种罕见且无法治愈的淋巴瘤。尚未进行比较评估有症状 WM 患者初始治疗疗效的对照研究。在这项研究中,我们比较了接受环磷酰胺-地塞米松-利妥昔单抗(CDR)、硼替佐米-地塞米松-利妥昔单抗(BDR)和苯达莫司汀-利妥昔单抗(Benda-R)初始治疗,以及初始治疗后接受利妥昔单抗维持治疗的 WM 患者的缓解和生存结局。分析中调整了与缓解和生存相关的相关临床因素。将利妥昔单抗维持治疗作为时变协变量进行分析。本研究纳入了 182 例患者,其中 57 例(31%)接受 Benda-R 治疗,87 例(48%)接受 BDR 治疗,38 例(21%)接受 CDR 治疗;116 例(64%)接受利妥昔单抗维持治疗。Benda-R 和 BDR 的最佳缓解时间短于 CDR(分别为 18、20 和 30 个月)。Benda-R 和 BDR 的无进展生存期(PFS)优于 CDR(分别为 5.5、5.8 和 4.8 年),10 年总生存率(OS)也优于 CDR(分别为 95%、96%和 81%)。与未接受维持治疗相比,接受利妥昔单抗维持治疗的患者缓解率更高(97% vs. 68%),中位 PFS 更长(6.8 年 vs. 2.8 年),10 年 OS 率更高(84% vs. 66%)。与 CDR 和无维持治疗相比,Benda-R、BDR 和利妥昔单抗维持治疗可使 WM 患者的缓解率更高,生存时间更长。

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