Bao Li, Lu Xi-jing, Zhang Xiao-hui, Huang Xiao-jun
Institute of Hematology of People's Hospital, Peking University, Beijing 100044, China.
Zhonghua Yi Xue Za Zhi. 2008 Jul 8;88(26):1829-31.
To investigate the efficacy and toxicity of bortezomib of different doses in combination with dexamethasone for the treatment of relapsed or refractory multiple myeloma (MM).
23 patients with relapsed or refractory MM, 10 males and 13 females, aged 65 (42-86), were randomized to 2 groups: low dose group receiving intravenous 1.0 mg/m2 bortezomib (n=10) on days 1, 4, 6, and 11 (twice weekly) combined with dexamethasone 20 mg/d on days 1-4, with 3 weeks as a course of treatment, and (20 standard dose group: receiving intravenous 1.3 mg/m2 bortezomib (n=13) combined with dexamethasone. The patients were followed up for 9.5 (3-15) months. The effect was determined using modified European Group for Blood and Marrow Transplantation (EBMT) criteria.
The complete response (CR) + partial response (PR) rate of the 1.0 mg/m2 bortezomib group was 70.0%, not significantly different from that of the 1.3 mg/m2 bortezomib group (61.5%, P > 0.05). The relief rate (CR + near CR rate) of the 1.0 mg/m2 bortezomib group was 20.0% not significantly different from that of the 1.3 mg/m2 bortezomib group (38.5%, P > 0.05). Only 1 case of adverse event over the grade 3 of National Cancer Institute Common Terminology Criteria for Adverse Events occurred in the 1.3 mg/m2 bortezomib group. Five cases of infectious fever and 2 cases of treatment-associated death occurred in the 1.3 mg/m2 bortezomib group.
Bortezomib at the dose of 1.3 mg/m2 is more effective in treatment of relapsed or refractory MM than that at the dose of 1.3 mg/m2 and has more side effects.
探讨不同剂量硼替佐米联合地塞米松治疗复发或难治性多发性骨髓瘤(MM)的疗效及毒性。
23例复发或难治性MM患者,男10例,女13例,年龄65岁(42 - 86岁),随机分为2组:低剂量组,第1、4、6和11天静脉滴注1.0 mg/m²硼替佐米(n = 10)(每周2次),并在第1 - 4天联合地塞米松20 mg/d,3周为1个疗程;(2)标准剂量组:静脉滴注1.3 mg/m²硼替佐米(n = 13)联合地塞米松。患者随访9.5个月(3 - 15个月)。采用改良的欧洲血液和骨髓移植组(EBMT)标准评估疗效。
1.0 mg/m²硼替佐米组的完全缓解(CR)+部分缓解(PR)率为70.0%,与1.3 mg/m²硼替佐米组(61.5%)差异无统计学意义(P > 0.05)。1.0 mg/m²硼替佐米组的缓解率(CR +接近CR率)为20.0%,与1.3 mg/m²硼替佐米组(38.5%)差异无统计学意义(P > 0.05)。1.3 mg/m²硼替佐米组仅发生1例美国国立癌症研究所不良事件通用术语标准3级以上不良事件。1.3 mg/m²硼替佐米组发生5例感染性发热和2例治疗相关死亡。
1.3 mg/m²剂量的硼替佐米治疗复发或难治性MM比1.0 mg/m²剂量更有效,但副作用更多。