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Modified Bortezomib-based Combination Therapy for Multiple Myeloma

An Open-Label Phase IV Study of the Efficacy of Bortezomib-based Combination Therapy the Treatment of Subjects With Multiple Myeloma

To investigate the efficacy of a modified bortezomib based combination therapy for patients with multiple myeloma.

研究概览

详细说明

Multiple myeloma (MM) is a common hematological malignancy in Chinese elderly population. The application of novel drugs improved the clinical outcome and survival of MM patients,even though MM remains an incurable hematological malignancy. Bortezomib is a typical one among these novel agents, its application resulted in great success, but its adverse events and high expense restricted its widely usage. Investigators modified the dose and frequency of bortezomib administration in combination therapy: Patients in the modified group received regimen with bortezomib (1.6mg/㎡) as an intravenous bolus once weekly on day 1, 8 in a 3 weeks cycle, in combination with dexamethasone,with or without doxorubicin/ cyclophosphamide/mitoxsnteone/thalidomide,while patients in the control group received similar combination therapy except with conventional bortezomib (1.3mg/㎡) administration twice weekly on day 1,4, 8,11.

The aim of this study is to investigate whether the modified bortezomib-based therapy may attain a similar efficacy as the conventional ones.

研究类型

介入性

注册 (实际的)

80

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Shanghai、中国、200080
        • Shanghai General Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 80年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Diagnosis of multiple myeloma based on standard diagnosis criteria:

    • plasmacytomas on tissue biopsy
    • bone marrow plasmacytosis
    • monoclonal immunoglobulin spike on serum electrophoresis
    • lytic bone lesions.
  • Must have relapsed or relapsed/refractory disease
  • 18 years of age or older
  • All baseline studies must be performed within 21 days of enrollment.
  • ECOG performance status of 0 to 2

Exclusion Criteria:

  • Renal insufficiency (serum creatinine levels > 2mg/dL)
  • Concomitant therapy medications that include corticosteroids
  • Peripheral neuropathy of Grade 3 or greater or painful Grade 2
  • Evidence of mucosal or internal bleeding and/or platelet refractory
  • ANC < 1000 cells/mm3
  • Hemoglobin < 8.0 g/dL
  • AST (SGOT and ALT) > 2 x ULN
  • Intolerance to bortezomib or CC-5013 in the past or significant allergy to either compound, boron or mannitol
  • Known hypersensitivity to thalidomide or the development of erythema nodosum
  • Active infection or serious co-morbid medical condition
  • Pregnant or breast-feeding women
  • Prior malignancy with the last three years except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, in situ breast cancer, on in-situ prostate cancer

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:modified BZ group
Patients with newly diagnosed or pre-treated MM(prior therapy not including bortezomib) received regimen with bortezomib (1.6mg/㎡) as an intravenous bolus once weekly on day 1, 8 in a 3 weeks cycle, in combination with dexamethasone,with or without doxorubicin/ cyclophosphamide/mitoxsnteone/thalidomide
其他名称:
  • 万珂
有源比较器:conventional BZ group
Patients with newly diagnosed or pre-treated MM(prior therapy not including bortezomib) received bortezomib (1.3mg/㎡) administration twice weekly on day 1,4, 8,11 in a 3 weeks cycle, in combination with dexamethasone,with or without doxorubicin/ cyclophosphamide/mitoxsnteone/thalidomide
其他名称:
  • 万珂

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
disease responses to treatment
大体时间:one year

Response evaluated by changes of serum M-component(g/L) through Serum quantitative immunoglobulins and Serum immunofixation electrophoresis.

(g/L)

one year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Guohua Liu, MD、Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2010年7月1日

初级完成 (预期的)

2018年10月1日

研究完成 (预期的)

2018年12月1日

研究注册日期

首次提交

2015年9月21日

首先提交符合 QC 标准的

2015年9月23日

首次发布 (估计)

2015年9月24日

研究记录更新

最后更新发布 (实际的)

2018年5月4日

上次提交的符合 QC 标准的更新

2018年5月3日

最后验证

2018年5月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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