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硼替佐米联合中剂量地塞米松及持续低剂量口服环磷酰胺治疗复发多发性骨髓瘤

Bortezomib in combination with intermediate-dose dexamethasone and continuous low-dose oral cyclophosphamide for relapsed multiple myeloma.

作者信息

Kropff Martin, Bisping Guido, Schuck Elke, Liebisch Peter, Lang Nicola, Hentrich Markus, Dechow Tobias, Kröger Nicolaus, Salwender Hans, Metzner Bernd, Sezer Orhan, Engelhardt Monika, Wolf Hans-Heinrich, Einsele Hermann, Volpert Sarah, Heinecke Achim, Berdel Wolfgang E, Kienast Joachim

机构信息

Department of Medicine/Haematology and Oncology, University of Muenster, Muenster, Germany.

出版信息

Br J Haematol. 2007 Aug;138(3):330-7. doi: 10.1111/j.1365-2141.2007.06656.x.

Abstract

A phase 2 trial was performed to study the combination of bortezomib (VELCADE) with intermediate-dose dexamethasone (DEX), and continuous low-dose oral cyclophosphamide (CY) in patients with relapsed multiple myeloma (MM). Fifty-four patients with advanced MM were enroled to receive eight 3-week treatment cycles with bortezomib 1.3 mg/m(2) on days 1, 4, 8, and 11, followed by three 5-week cycles with bortezomib 1.3 mg/m(2) on days 1, 8, 15, and 22. Within all cycles, DEX 20 mg/d was given orally on the day of bortezomib injection and the day thereafter. In addition, patients received CY continuous oral treatment at a dose of 50 mg/d p.o. once daily. Fifty patients completing at least one treatment cycle were evaluable for response. Complete, partial, and minor responses occurred in 16%, 66% and 8% of patients, respectively; overall response rate 90% (efficacy analysis). Median event-free survival was 12 months, with a median overall survival of 22 months. Adverse events (AE) of grades 3 or 4 occurring in at least 10% of patients comprised leucopenia, infection, herpes zoster, thrombocytopenia, neuropathy and fatigue. Bortezomib combined with DEX and CY is a highly effective treatment for relapsed MM at an acceptable rate of grade 3/4 AE. Antiviral prophylaxis appears to be mandatory.

摘要

开展了一项2期试验,以研究硼替佐米(万珂)与中等剂量地塞米松(DEX)以及持续低剂量口服环磷酰胺(CY)联合用于复发多发性骨髓瘤(MM)患者的疗效。54例晚期MM患者入组,接受8个为期3周的治疗周期,在第1、4、8和11天给予硼替佐米1.3mg/m²,随后接受3个为期5周的周期,在第1、8、15和22天给予硼替佐米1.3mg/m²。在所有周期中,在硼替佐米注射当天及之后一天口服给予DEX 20mg/d。此外,患者接受CY持续口服治疗,剂量为每日50mg口服。50例完成至少一个治疗周期的患者可评估疗效。完全缓解、部分缓解和微小缓解分别发生在16%、66%和8%的患者中;总缓解率为90%(疗效分析)。中位无事件生存期为12个月,中位总生存期为22个月。至少10%的患者发生的3级或4级不良事件包括白细胞减少、感染、带状疱疹、血小板减少、神经病变和疲劳。硼替佐米联合DEX和CY是复发MM的一种高效治疗方法,3/4级不良事件发生率可接受。抗病毒预防似乎是必需的。

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