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临床试验/NCT03061656
NCT03061656Unknown2 期

High-dose 131I-MIBG Treatment Incorporated Into Tandem High-dose Chemotherapy and Autologous Stem Cell Transplantation in Patients With High-risk Neuroblastoma

Samsung Medical Center0 个研究点目标入组 40 人开始时间: 2009年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
40
主要终点
Rate of event free survival

研究概览

简要总结

The purpose of this study is to evaluate the efficacy and toxicity of tandem HDCT/ASCT including high-dose 131I-metaiodobenzylguanidine (MIBG) treatment. In the present study, a single arm trial of tandem HDCT/ASCT will be carried out.

详细描述

Although the outcome of high-risk neuroblastoma has improved after the introduction of HDCT/ASCT, the outcome was still unsatisfactory with 30-40% of survival. We previously reported the results of a single arm prospective trial (SMC NB-2004 study) using tandem HDCT/auto-SCT for high-risk neuroblastoma. In the NB-2004 trial, total body irradiation (TBI) was incorporated in second transplantation. Survival rates were very encouraging; however, short- and long-term toxicities associated with tandem HDCT/auto-SCT, particularly TBI, were also very significant. For this reason, we designed a new prospective trial (SMC NB-2009 study), in which only TBI in the second HDCT/auto-SCT of NB-2004 study was substituted with high-dose 131I-MIBG treatment in order to reduce short- and long-term toxicities without jeopardizing survival rate.

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

  • Patients with high-risk neuroblastoma

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 (high-dose 131I-MIBG, 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 (high-dose 131I-MIBG, 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 (high-dose 131I-MIBG, 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 (high-dose 131I-MIBG, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: 131I-MIBG (Radiation)

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 (high-dose 131I-MIBG, 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 (high-dose 131I-MIBG, thiotepa, melphalan)
  1. Local radiotherapy
  2. Retinoic acid, interleukin-2

干预措施: Melphalan (Drug)

结局指标

主要结局

Rate of event free survival

时间窗: Up to 5 years

Event is defined as relapse, disease progression or treatment-related mortality.

次要结局

  • Rate of treatment-related adverse events as assessed by CTCAE v4.0(Up to 5 years)

研究者

申办方类型
Other
责任方
Sponsor

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