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硼替佐米联合持续低剂量环磷酰胺和地塞米松治疗后,给予一年维持治疗复发多发性骨髓瘤患者。

Combination therapy with bortezomib, continuous low-dose cyclophosphamide and dexamethasone followed by one year of maintenance treatment for relapsed multiple myeloma patients.

机构信息

Department of Haematology, University Medical Centre Groningen, Groningen, The Netherlands.

Department of Research, Netherlands Comprehensive Cancer Organisation, Utrecht, The Netherlands.

出版信息

Br J Haematol. 2015 Dec;171(5):720-5. doi: 10.1111/bjh.13653. Epub 2015 Sep 11.

Abstract

Combination therapy for longer periods but at low dose might be an effective and tolerable manner to treat patients with relapsed multiple myeloma (MM). We used bortezomib, dexamethasone and low-dose oral cyclophosphamide as an induction regimen, followed by 1 year of maintenance consisting of bortezomib and cyclophosphamide. Relapsed MM patients were treated with six cycles of bortezomib twice weekly, cyclophosphamide 50 mg daily and dexamethasone. Maintenance therapy was given for 1 year. Primary endpoints were toxicity during re-induction and maintenance therapy. Secondary endpoints were response to treatment and progression-free (PFS) and overall survival (OS). This study included 59 patients. Myelosuppression and neuropathy were the most common side effects. Median follow-up was 27·1 (0·46-54·4) months with an overall response of 71%, and a very good partial response or more of 33%. During maintenance, improved responsiveness was observed in 19% of the patients. The median PFS was 18·4 months (range 0·13-43·5) and the median OS was 28·1 months (range 0·13-54·4). In conclusion, our study demonstrates that treatment with bortezomib, dexamethasone and low-dose cyclophosphamide is an effective and manageable regimen. Adding 1 year of maintenance was feasible, with limited side effects and an increased response rate.

摘要

联合治疗延长时间但剂量较低可能是治疗复发性多发性骨髓瘤(MM)患者的有效且耐受良好的方法。我们使用硼替佐米、地塞米松和低剂量口服环磷酰胺作为诱导方案,随后进行为期 1 年的维持治疗,包括硼替佐米和环磷酰胺。复发性 MM 患者接受 6 个周期的硼替佐米每周 2 次、环磷酰胺 50mg 每日和地塞米松治疗。维持治疗持续 1 年。主要终点是再诱导和维持治疗期间的毒性。次要终点是治疗反应、无进展生存期(PFS)和总生存期(OS)。本研究纳入了 59 例患者。骨髓抑制和周围神经病变是最常见的副作用。中位随访时间为 27.1 个月(0.46-54.4),总体缓解率为 71%,非常好的部分缓解或更好的缓解率为 33%。在维持治疗期间,19%的患者观察到反应改善。中位 PFS 为 18.4 个月(0.13-43.5),中位 OS 为 28.1 个月(0.13-54.4)。总之,我们的研究表明,硼替佐米、地塞米松和低剂量环磷酰胺的治疗是一种有效且易于管理的方案。添加 1 年的维持治疗是可行的,副作用有限,且反应率增加。

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