跳至主要内容
临床试验/NCT00610883
NCT00610883已完成2 期

LSA4 Protocol for the Treatment of Advanced Pediatric and Adolescent Non-Hodgkins Lymphoma

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 1990年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
17
试验地点
1
主要终点
Complete Remission

研究概览

简要总结

Non-Hodgin's lymphoma is curable in 76% of patients. In nonlymphoblastic lymphmas, cancer may return on average 3 months from beginning treatment and for lymphoblastic lymphomas, 6 months. To aggressively treat this cancer this study uses effective drugs in three parts:

  • Induction ends on day 19
  • Consolidation ends on day 38 or 42
  • Maintenance may include up to 6 cycles

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Non-Hodgkin's Lymphoma stages III, IV, IVA with
  • T cell lymphomas, any primary site irrespective of LDH level
  • large cell lymphomas, any primary site irrespective of LDH level
  • B cell lymphomas, any primary site with initial LDH of less than 500

排除标准

  • B cell lymphomas, any primary site with initial LDH of less than 500 and initial CNS or bone involvement

研究组 & 干预措施

1 - LSA4

Experimental

干预措施: LSA4, Cyclophosphamide, Methotrexate, Daunomycin, L-asparaginase, BCNU (Drug)

结局指标

主要结局

Complete Remission

时间窗: 330 Days

The number of patients who achieved a complete remission as a result of treatment

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验