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临床试验/NCT02504190
NCT02504190已完成不适用

Non-interventional Study Evaluating Efficacy and Tolerance on TEAM Conditioning (Thiotepa/Etoposide/Aracytin/Melphalan) Followed by Autologous Haematopoietic Stem Cells Transplantation in Patients With Lymphoma

Association for Training, Education, and Research in Hematology, Immunology, and Transplantation1 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2015年7月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
95
试验地点
1
主要终点
Progression free survival (PFS)

研究概览

简要总结

Lymphoma is a malignant blood disease sensitive to chemotherapy. In case of relapse after first-line treatment, high-dose chemotherapy conditioning followed by autologous hematopoietic stem cell transplantation (auto-HSCT) improves patient survival and reduces the risk of relapse. Auto-HSCT may also be indicated in the first line in case of aggressive lymphoma at high risk of relapse. BEAM (Carmustine, Etoposide, Aracytine and Melphalan) is the more frequently used high-dose conditioning regimen. Nevertheless, Carmustine is no longer available in Europe.

The investigators have therefore chosen to replace Carmustine by Thiotepa and use the TEAM regimen as the new conditioning. Indeed, Thiotepa is approved by french national agency for the security of drugs (ANSM) for use as part of auto-HSCT conditioning regimen. The results of TEAM regimen in terms of efficacy and toxicity appear similar to those of BEAM. However, no study have been performed prospectively. Only small series and case reports have been reported.

If the study confirms the results of retrospective studies, conditioning by TEAM could become a new standard in auto-HSCT for the treatment of lymphoma.

This study is non-interventional, prospective with 3 centers.

All included patients will receive, according to standard practice and drug label in France, the following diagram:

  1. Conditioning:
  • Thiotepa 8 mg / kg to J-6
  • Etoposide 100 mg / m² / 12 h for 4 days (J-5 to D-2)
  • Aracytine 200 mg / m² / 12 h for 4 days (J-5 to D-2)
  • Melphalan 140 mg / m² on day-1
  1. Transfusion graft: the day D0 with autologous peripheral stem cell transplant
  2. Care supports: Patients will be treated according to the usual procedures of centers participating in the study at the discretion of the investigator.
  3. Follow-up of patients will not be changed by the study.

The main objective of the study is to evaluate the progression-free survival (PFS) of lymphoma patients treated with autologous stem cells after conditioning by TEAM

Secondary objectives are:

  • To evaluate overall survival;
  • To assess the response to treatment;
  • to evaluate the incidence of relapse;
  • to assess the toxic transplant related mortality;
  • to study transplant-related morbidity (infections, nutritional and gastrointestinal toxicity, immune reconstitution).

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 18 and 65 years,
  • lymphoma confirmed by biopsy
  • first autologous haematopoietic stem cells transplantation after TEAM conditioning

排除标准

  • VIH, HBV, and/or HCV seropositive
  • Contraindication to autologous stem cell transplantation

结局指标

主要结局

Progression free survival (PFS)

时间窗: 1 year after autologous haematopoietic stem cells transplantation

次要结局

  • Incidence of infections(during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation)
  • Overall Survival(100 days and at 1 year after autologous haematopoietic stem cells transplantation)
  • Incidence of relapse(100 days and 1 year after autologous haematopoietic stem cells transplantation)
  • Incidence of grade 3-4 side effects(during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation)
  • Overall and complete response rate(100 days and 1 year after autologous haematopoietic stem cells transplantation)
  • Impact of transplant-related mortality(100 days and 1 year after autologous haematopoietic stem cells transplantation)

研究者

发起方
Association for Training, Education, and Research in Hematology, Immunology, and Transplantation
申办方类型
Other
责任方
Sponsor

研究点 (1)

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