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硼替佐米对复发的高危及老年多发性骨髓瘤患者的安全性与疗效

Safety and efficacy of bortezomib in high-risk and elderly patients with relapsed multiple myeloma.

作者信息

Richardson Paul G, Sonneveld Pieter, Schuster Michael W, Irwin David, Stadtmauer Edward A, Facon Thierry, Harousseau Jean-Luc, Ben-Yehuda Dina, Lonial Sagar, San Miguel Jesús-F, Cavenagh Jamie D, Anderson Kenneth C

机构信息

Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.

出版信息

Br J Haematol. 2007 Jun;137(5):429-35. doi: 10.1111/j.1365-2141.2007.06585.x. Epub 2007 Apr 19.

Abstract

Adverse prognostic factors in multiple myeloma include advanced age, number of prior therapies, and higher International Staging System (ISS) disease stage. In the international, randomised, phase-3 Assessment of Proteasome Inhibition for Extending Remissions (APEX) study, bortezomib demonstrated significantly longer time to progression (TTP), higher response rates and improved survival compared with high-dose dexamethasone in patients with relapsed multiple myeloma following one to three prior therapies. In this APEX subgroup analysis, efficacy of bortezomib and dexamethasone was compared in elderly (age > or =65 years) and high-risk (>1 prior line of therapy; ISS stage II/III; refractory to prior therapy) patients. Bortezomib demonstrated substantial clinical activity in these patients. Response rate (34-40% vs. 13-19%), including complete response rate (5-8% vs. 0-1%), was significantly higher with bortezomib versus dexamethasone in all four subgroups. Similarly, median TTP was significantly longer with bortezomib versus dexamethasone, and 1-year survival probability was significantly higher in all subgroups. As in the total APEX population, rates of grade 3/4 adverse events were higher in bortezomib- versus dexamethasone-treated patients aged > or =65 years and with >1 prior line, while rates of serious adverse events were similar; toxicities generally proved manageable. Bortezomib should be considered an appropriate treatment for elderly and high-risk patients with relapsed multiple myeloma.

摘要

多发性骨髓瘤的不良预后因素包括高龄、既往治疗次数以及较高的国际分期系统(ISS)疾病分期。在国际随机3期蛋白酶体抑制延长缓解期评估(APEX)研究中,与接受高剂量地塞米松治疗的1 - 3线既往治疗后复发的多发性骨髓瘤患者相比,硼替佐米显示出显著更长的疾病进展时间(TTP)、更高的缓解率以及更好的生存率。在这项APEX亚组分析中,对老年(年龄≥65岁)和高危(>1线既往治疗;ISS II/III期;对既往治疗耐药)患者中硼替佐米和地塞米松的疗效进行了比较。硼替佐米在这些患者中显示出显著的临床活性。在所有四个亚组中,硼替佐米组的缓解率(34 - 40%对13 - 19%),包括完全缓解率(5 - 8%对0 - 1%)均显著高于地塞米松组。同样,硼替佐米组的中位TTP显著长于地塞米松组,且所有亚组的1年生存概率均显著更高。与整个APEX研究人群一样,在年龄≥65岁且既往治疗线数>1的患者中,接受硼替佐米治疗的患者3/4级不良事件发生率高于接受地塞米松治疗的患者,而严重不良事件发生率相似;毒性通常可控。硼替佐米应被视为老年和高危复发多发性骨髓瘤患者的合适治疗药物。

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