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首页> 外文期刊>The Lancet >Bortezomib with thalidomide plus dexamethasone compared with thalidomide plus dexamethasone as induction therapy before, and consolidation therapy after, double autologous stem-cell transplantation in newly diagnosed multiple myeloma: a randomised phase 3 study
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Bortezomib with thalidomide plus dexamethasone compared with thalidomide plus dexamethasone as induction therapy before, and consolidation therapy after, double autologous stem-cell transplantation in newly diagnosed multiple myeloma: a randomised phase 3 study

机译:与沙利度胺加上地塞米松的Bortezomib与沙利度胺加上地塞米松作为诱导治疗,并在新诊断出的多发性骨髓瘤中双重自体茎细胞移植:随机相3研究

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Background Thalidomide plus dexamethasone (TD) is a standard induction therapy for myeloma. We aimed to assess the efficacy and safety of addition of bortezomib to TD (VTD) versus TD alone as induction therapy before, and consolidation therapy after, double autologous stem-cell transplantation in newly diagnosed multiple myeloma.Methods Patients (aged 18-65 years) with previously untreated symptomatic myeloma were enrolled from 73 sites in Italy between May, 2006, and April, 2008, and data collection continued until June 30, 2010. Patients were randomly allocated (1:1 ratio) by a web-based system to receive three 21-day cycles of thalidomide (100 mg daily for the first 14 days and 200 mg daily thereafter) plus dexamethasone (40 mg daily on 8 of the first 12 days, but not consecutively; total of 320 mg per cycle), either alone or with bortezomib (1-3 mg/m on days 1, 4, 8, and 11). The randomisation sequence was computer generated by the study coordinating team and was stratified by disease stage. After double autologous stem-cell transplantation, patients received two 35-day cycles of their assigned drug regimen, VTD or TD, as consolidation therapy. The primary endpoint was the rate of complete or near complete response to induction therapy. Analysis was by intention to treat. Patients and treating physicians were not masked to treatment allocation. This study is still underway but is not recruiting participants, and is registered with ClinicalTrials.gov, number NCT01134484, and with EudraCX number 2005-003723-39.
机译:背景,沙利度胺加上地塞米松(TD)是骨髓瘤的标准诱导疗法。我们的旨在评估Bortezomib向TD(VTD)的疗效和安全性与TD以前的感应治疗,并在新诊断出的多发性骨髓瘤中双重自体干细胞移植治疗。方法(18-65岁)以前未经治疗的症状骨髓瘤在2006年5月至2008年5月至4月30日之间从意大利的73个遗址注册了73个地点,并通过基于网络的系统随机分配(1:1比例),患者进行数据收集接受三个21天的沙利度胺(每日100毫克,每天每天200毫克)加上地塞米松(每天40毫克,在前12天的8天,但不连续;每周期总数为320毫克)单独或用硼替佐米(1-3 mg / m,在第1,4,8和11天)。随机化序列是由研究协调团队产生的计算机,并通过疾病阶段分层。在双重自体干细胞移植后,患者接受其分配的药物方案,VTD或TD的35天循环,作为合并治疗。主要终点是对感应治疗的完全或接近完全反应的速度。分析是意图治疗。患者和治疗医生没有掩盖治疗分配。这项研究仍然正在进行中,但不是招聘参与者,并在Clincoicaltrial.gov,nct0113484和Eudracx号码2005-003723-39注册。

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