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临床试验/NCT00793845
NCT00793845已完成2 期

Tandem High-dose Chemotherapy and Autologous Stem Cell Rescue in Patients With High-risk Neuroblastoma

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2008年8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
40
试验地点
1
主要终点
Overall survival and event-free survival, short-term and long-term toxicity of tandem high-dose chemotherapy and autologous stem cell transplantation

研究概览

简要总结

The purpose of this study is to evaluate the efficacy and toxicity of tandem HDCT/ASCR in children with high-risk neuroblastoma. In the present study, a single arm trial of tandem HDCT/ASCR will be carried out. In the present study, the investigators will investigate whether tandem HDCT/ASCR might improve the survival of patients with high-risk neuroblastoma with acceptable toxicity.

详细描述

The prognosis of high-risk neuroblastoma after conventional chemoradiotherapy is generally poor. Therefore, a strategy using high-dose chemotherapy and autologous stem cell rescue (HDCT/ASCR) has been explored to improve the prognosis of patients with high-risk neuroblastoma. This strategy is based on the hypothesis that dose escalation might improve the survival of children with high-risk neuroblastoma. The results of randomized trials comparing HDCT/ASCR with chemotherapy alone showed a better event-free survival (EFS) in the HDCT/ASCR arm than in the continuous chemotherapy arm. However, the overall EFS was unsatisfactory.

In this context, investigators have examined the efficacy of double or triple tandem HDCT/ASCR to further improve the outcome of high-risk neuroblastoma patients. George et al. carried out a single arm trial of tandem transplantation as consolidation therapy, and reported improved long-term survival (5-year progression-free survival 47%) with acceptable toxicity. Kletzel et al. also conducted a single arm trial of triple tandem transplantation and reported improved survival (3-year EFS 57%). They demonstrated that further dose escalation using sequential HDCT/ASCR might result in further improvements in the survival of patients with high-risk neuroblastoma.

Investigators in the present study also carried out tandem transplantation as consolidation therapy, and reported improved long-term survival (5-year progression-free survival 62%) with acceptable toxicity. However, throughout our previous study, multiple modifications were made in the treatment plan, which resulted in significant variability over time between patients. This variability may create doubt as to whether tandem HDCT/ASCR itself resulted in the improved outcome. In addition, toxic death rate was relatively high (15.4%), although final survival rate was very high (best survival rate ever reported). Therefore, prospective study is needed to evaluate the efficacy and toxicity of tandem HDCT/ASCR.

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

性别
All
接受健康志愿者

入选标准

  • Patients with high-risk neuroblastoma
  • Patients with intermediate-risk neuroblastoma if gross tumor remained after surgery

排除标准

  • Patients with progressive disease before high-dose chemotherapy
  • Patients whose parents want to stop or change the planned treatment
  • Patients with organ toxicities of NCI grade >2 before high-dose chemotherapy

研究组 & 干预措施

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Cyclophosphamide (Drug)

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Etoposide (Drug)

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Carboplatin (Drug)

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Thiotepa (Drug)

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Melphalan (Drug)

High risk neuroblastoma

Experimental
  1. Conventional chemotherapy (9 cycles)
  2. Surgery conventional chemotherapy (after 6 cycles of chemotherapy)
  3. Tandem HDCT/autoSCT
  • First HDCT (cyclophosphamide, etoposide, carboplatin)
  • Second HDCT (total body irradiation, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Total body irradiation (Radiation)

结局指标

主要结局

Overall survival and event-free survival, short-term and long-term toxicity of tandem high-dose chemotherapy and autologous stem cell transplantation

时间窗: from 1 year after second high-dose chemotherapy

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)

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