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在套细胞淋巴瘤中,采用 VcR-CVAD 诱导化疗联合维持利妥昔单抗治疗:威斯康星肿瘤网络研究。

VcR-CVAD induction chemotherapy followed by maintenance rituximab in mantle cell lymphoma: a Wisconsin Oncology Network study.

机构信息

Department of Medicine, School of Medicine and Public Health, The UW Carbone Cancer Center, University of Wisconsin, Madison, WI 53705, USA.

出版信息

Br J Haematol. 2011 Oct;155(2):190-7. doi: 10.1111/j.1365-2141.2011.08820.x. Epub 2011 Aug 16.

Abstract

Intensive chemotherapy regimens are not feasible in many adults with mantle cell lymphoma (MCL). We sought to build upon our previous experience with a non-intensive regimen, modified R-hyperCVAD chemotherapy (rituximab, cyclophosphamide, vincristine, doxorubicin, dexamethasone) with maintenance rituximab (MR), by the incorporation of bortezomib (VcR-CVAD) and the extension of MR beyond 2 years. Patients with previously untreated MCL received VcR-CVAD chemotherapy every 21 d for six cycles. Patients achieving at least a partial response to induction chemotherapy received rituximab consolidation (375 mg/m(2) × 4 weekly doses) and MR (375 mg/m(2) every 12 weeks × 20 doses). The primary end points were overall and complete response (CR), and secondary endpoints were progression-free (PFS) and overall survival (OS). Thirty patients were enrolled, with a median age of 61 years. All patients had advanced stage disease, and 60% had medium/high MCL International Prognostic Index risk factors. A CR or unconfirmed CR was achieved in 77% of patients. After a median follow-up of 42 months, the 3-year PFS and OS were 63% and 86%, respectively. The observed 3-year PFS and OS with VcR-CVAD in MCL were comparable to reported outcomes with more intensive regimens. A cooperative group trial (E1405) is attempting to replicate these promising results.

摘要

在许多套细胞淋巴瘤 (MCL) 成人患者中,强化化疗方案并不可行。我们试图在以前使用非强化方案的基础上进一步探索,即改良 R-hyperCVAD 化疗(利妥昔单抗、环磷酰胺、长春新碱、多柔比星、地塞米松)联合维持治疗利妥昔单抗(MR),在此基础上加入硼替佐米(VcR-CVAD),并将 MR 延长至 2 年以上。未经治疗的 MCL 患者每 21 天接受一次 VcR-CVAD 化疗,共 6 个周期。诱导化疗至少达到部分缓解的患者接受利妥昔单抗巩固治疗(375mg/m2×4 周剂量)和 MR(375mg/m2 每 12 周×20 剂量)。主要终点是总缓解率和完全缓解率(CR),次要终点是无进展生存期(PFS)和总生存期(OS)。共纳入 30 例患者,中位年龄为 61 岁。所有患者均患有晚期疾病,60%有中/高危 MCL 国际预后指数危险因素。77%的患者达到 CR 或未确认的 CR。中位随访 42 个月后,3 年 PFS 和 OS 分别为 63%和 86%。在 MCL 中,观察到的 3 年 PFS 和 OS 与更强化的方案相当。一项合作组试验(E1405)正在试图复制这些有希望的结果。

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