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Meeting highlights from: The 50th annual meeting of the American society of hematology; San Francisco, CA; December 6-9, 2008

机译:会议摘要来自:美国血液学会第50届年会;加利福尼亚州旧金山; 2008年12月6日至9日

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摘要

The addition of bortezomib to melpha-lan plus prednisone (VMP) has yielded substantial clinical benefit in patients with multiple myeloma (MM) not proceeding to transplantation, and first-line VMP is now approved by the Food and Drug Administration for transplantation-ineligible patients with MM. In a phase I/II trial, VMP yielded a 32% complete response (CR) rate, and the overall survival (OS) rate was 85% at 38 months compared with 38% with MP.2 The phase III VISTA (Velcade as Initial Standard Therapy) trial randomized patients to VMP versus melphalan/predni-sone alone (MP) with a primary endpoint of time to progression (TTP).
机译:在未进行移植的多发性骨髓瘤(MM)患者中,将硼替佐米添加到美法仑加泼尼松(VMP)中已产生了可观的临床益处,并且食品和药物管理局现已批准一线VMP用于不适合移植的患者与MM。在I / II期试验中,VMP产生了32%的完全缓解(CR)率,38个月时的总生存率(OS)为85%,而MP为38%。2III期VISTA(Velcade为初始(标准疗法)试验将患者随机分为VMP与单独使用美法仑/泼尼松(MP),主要终点为进展时间(TTP)。

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