跳至主要内容
临床试验/NCT01362972
NCT01362972已完成不适用

Analysis of Data Collected in the European Group for Blood and Marrow Transplantation (EBMT) Registry on a Cohort of Patients Receiving Plerixafor

Genzyme, a Sanofi Company0 个研究点目标入组 7,801 人开始时间: 2011年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
7,801
主要终点
Compare PFS, OS, and Relapse in EBMT-registered autoHSC transplant patients between 2008 and 2012, with HSCs mobilized with Plerixafor + G-CSF vs other regimens.

研究概览

简要总结

In the European Union (EU), plerixafor is indicated in combination with granulocyte colony stimulating factor (G-CSF) to enhance mobilisation of haematopoietic stem cells (HSCs) to the peripheral blood (PB) for collection and subsequent autologous transplantation in patients with lymphoma and multiple myeloma (MM) whose cells mobilise poorly.

This is a clinical outcome analysis of a prospectively defined cohort of patients with data reported retrospectively to the European Group for Blood and Marrow Transplantation (EBMT) who have lymphoma or multiple myeloma (MM), whose cells mobilize poorly, and who have undergone autologous haematopoietic stem cell (HSC) transplantation during the years 2008 up to and including 2012.

The EBMT is a non-profit, scientific society representing more than 600 transplant centers mainly in Europe. The EBMT promotes all activity aiming to improve stem cell transplantation or cellular therapy, which includes registering all the activity relating to stem cell transplants. Data are entered, managed, and maintained in a central database with internet access; each EBMT center is represented in this database.

The analysis of data from a well established registry like the EBMT registry allows for follow up of a large number of patients who are representative of the patient population receiving plerixafor.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For inclusion in the cohort analysis, patients must have data in the EBMT registry that meet the following criteria:
  • Adults diagnosed with lymphoma or multiple myeloma (MM)
  • Received first autologous transplants of peripheral blood (PB) non ex-vivo manipulated stem cells in the time period listed above using cells mobilised with one of the following regimens:
  • plerixafor plus granulocyte colony stimulating factor (G-CSF)
  • plerixafor plus G-CSF plus chemotherapy
  • G-CSF alone or
  • G-CSF plus chemotherapy
  • Note: Patients included in the plerixafor groups will be those treated according to the label
  • Provision of informed consent (i.e., all patients with data in the EBMT registry will have signed consent at the time of transplantation for the potential use of their data for analysis)

排除标准

  • Patients treated with plerixafor NOT according to the European Union (EU) label.
  • Patients whose graft product underwent ex vivo manipulation will be excluded from analysis

结局指标

主要结局

Compare PFS, OS, and Relapse in EBMT-registered autoHSC transplant patients between 2008 and 2012, with HSCs mobilized with Plerixafor + G-CSF vs other regimens.

时间窗: 5 Years

次要结局

未报告次要终点

研究者

发起方
Genzyme, a Sanofi Company
申办方类型
Industry
责任方
Sponsor

相似试验

Analysis of Data Collected in the European Group for... | 临床试验