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Non-interventional Study on TEAM Conditioning in Patients With Lymphoma (TEAM)

Completed
Conditions
Lymphoma
Registration Number
NCT02504190
Lead Sponsor
Association for Training, Education, and Research in Hematology, Immunology, and Transplantation
Brief Summary

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

2. Transfusion graft: the day D0 with autologous peripheral stem cell transplant

3. Care supports: Patients will be treated according to the usual procedures of centers participating in the study at the discretion of the investigator.

4. 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).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
95
Inclusion Criteria
  • Patients aged between 18 and 65 years,
  • lymphoma confirmed by biopsy
  • first autologous haematopoietic stem cells transplantation after TEAM conditioning
Exclusion Criteria
  • VIH, HBV, and/or HCV seropositive
  • Contraindication to autologous stem cell transplantation

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression free survival (PFS)1 year after autologous haematopoietic stem cells transplantation
Secondary Outcome Measures
NameTimeMethod
Incidence of infectionsduring aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation
Overall Survival100 days and at 1 year after autologous haematopoietic stem cells transplantation
Incidence of relapse100 days and 1 year after autologous haematopoietic stem cells transplantation
Incidence of grade 3-4 side effectsduring aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation
Overall and complete response rate100 days and 1 year after autologous haematopoietic stem cells transplantation
Impact of transplant-related mortality100 days and 1 year after autologous haematopoietic stem cells transplantation

Trial Locations

Locations (1)

Mohamad Mohty

🇫🇷

Paris, France

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