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维持利妥昔单抗治疗套细胞淋巴瘤诱导化疗免疫治疗后:威斯康星肿瘤网络的一项先导研究的长期随访结果。

Maintenance rituximab following induction chemo-immunotherapy for mantle cell lymphoma: long-term follow-up of a pilot study from the Wisconsin Oncology Network.

机构信息

Department of Medicine, University of Wisconsin, Madison, WI, USA.

出版信息

Leuk Lymphoma. 2011 Sep;52(9):1675-80. doi: 10.3109/10428194.2011.580404.

Abstract

Mantle cell lymphoma (MCL) is challenging to manage, with a median survival of 3-5 years. While intensive strategies are often appropriate for younger patients, these approaches are often not appropriate for older patients. In 2006, we reported our initial results using modified R-hyperCVAD (rituximab with hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone) with maintenance rituximab. The complete response rate was 64%, and median progression-free survival (PFS) 37 months. Herein, we update our results, now with a median follow-up of 62 months. The median PFS is unchanged and the median overall survival (OS) is 70 months. The proportion of patients surviving at 5 years is 62%, comparable to studies using intensive strategies in similar patient populations. No late toxicities were noted in our cohort. These long-term results suggest that the modified R-hyperCVAD regimen with maintenance rituximab is an excellent option for older patients with newly diagnosed mantle cell lymphoma.

摘要

套细胞淋巴瘤(MCL)的治疗具有挑战性,中位生存期为 3-5 年。虽然强化策略通常适用于年轻患者,但这些方法通常不适用于老年患者。2006 年,我们报告了使用改良的 R-hyperCVAD(利妥昔单抗联合超分割环磷酰胺、长春新碱、多柔比星和地塞米松)联合维持利妥昔单抗治疗的初步结果。完全缓解率为 64%,中位无进展生存期(PFS)为 37 个月。在此,我们更新了我们的结果,现在的中位随访时间为 62 个月。中位 PFS 未改变,中位总生存期(OS)为 70 个月。5 年生存率为 62%,与在类似患者人群中使用强化策略的研究相当。我们的队列中未观察到迟发性毒性。这些长期结果表明,改良的 R-hyperCVAD 方案联合维持利妥昔单抗是新诊断的套细胞淋巴瘤老年患者的绝佳选择。

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