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蛋白酶体抑制用于治疗多发性骨髓瘤:临床进展

Proteasome inhibition for treatment of multiple myeloma: clinical update.

作者信息

Stadtmauer Edward A

机构信息

Myeloma Program, University of Pennsylvania Cancer Center, Philadelphia, Pennsylvania 19104, USA.

出版信息

J Natl Compr Canc Netw. 2004 Nov;2 Suppl 4:S10-5.

Abstract

Multiple myeloma is an incurable hematologic cancer affecting over 50,000 Americans. Current treatment approaches employ various chemotherapeutic regimens; however, relapse is inevitable. A novel treatment for multiple myeloma is bortezomib, a proteasome inhibitor that has shown significant in vitro and in vivo activity. Bortezomib, recently approved by the FDA, has activity in patients with relapsed and refractory multiple myeloma. A clinical update from the SUMMIT and CREST phase II trials is presented; overall response rates were 35% and 38%, respectively, for the 1.3 mg/m2 dose of bortezomib. Side effects, including thrombocytopenia and peripheral neuropathy, are generally manageable APEX, a phase III trial of bortezomib compared to high-dose dexamethasone in multiple myeloma patients who had received 1-3 prior therapies, was stopped early due to superior efficacy on the bortezomib arm.

摘要

多发性骨髓瘤是一种无法治愈的血液系统癌症,影响着超过5万名美国人。目前的治疗方法采用各种化疗方案;然而,复发是不可避免的。一种针对多发性骨髓瘤的新型治疗药物是硼替佐米,它是一种蛋白酶体抑制剂,已在体外和体内显示出显著活性。硼替佐米最近已获美国食品药品监督管理局(FDA)批准,对复发和难治性多发性骨髓瘤患者有治疗活性。本文介绍了SUMMIT和CREST二期试验的临床最新情况;对于1.3mg/m²剂量的硼替佐米,总体缓解率分别为35%和38%。包括血小板减少症和周围神经病变在内的副作用通常是可控的。APEX是一项三期试验,在接受过1 - 3次前期治疗的多发性骨髓瘤患者中,将硼替佐米与高剂量地塞米松进行比较,由于硼替佐米组疗效更佳,该试验提前终止。

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