跳至主要内容
临床试验/NCT01813344
NCT01813344Unknown不适用

The Clinical Outcomes of Hyper-CVAD Treatment in Lymphoblastic Lymphoma

Ajou University School of Medicine1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
50
试验地点
1
主要终点
Overall survival

研究概览

简要总结

Treatment outcomes of lymphoblastic lymphoma (LBL) have improved by the use of the regimens for acute lymphoblastic leukemia. Hyper-CVAD is one of the most effective treatments with high remission rate in acute lymphoblastic leukemia (ALL) and LBL. However, the treatment outcome of hyper-CVAD in LBL has reported only in small number of patients from single institution. The investigators conducted this study to evaluate the hyper-CVAD regimen based treatment in LBL.

详细描述

We will analyze treatment outcome of lymphoblastic lymphoma patients treated with hyper-CVAD regimen from 13 institutions in Korea. In all patients, hyper-CVAD was initial treatment. After achievement of response, patients either underwent hematopoietic stem cell transplantation (HSCT) or consolidation with hyper-CVAD.

研究设计

研究类型
Observational
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

  • age over 18 at diagnosis
  • Pathologically proven lymphoblastic lymphoma

排除标准

  • proven HIV infection
  • pretreatment with other regimens

结局指标

主要结局

Overall survival

时间窗: 3-year

Progression free survival

时间窗: 3-year

次要结局

  • Response Rate(24 weeks)

研究者

发起方
Ajou University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Seong Hyun Jeong

Assistant professor

Ajou University School of Medicine

研究点 (1)

Loading locations...

相似试验