An observational study in Lymphoma, sponsored by Association for Training, Education, and Research in Hematology, Immunology, and Transplantation. Completed at 1 site in France. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2020-05-20.
Sponsored by Association for Training, Education, and Research in Hematology, Immunology, and Transplantation · Observational
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:
Conditioning:
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:
5,624 studies on the registry are indexed under Lymphoma; 824 are open to participants now.
This study's enrollment of 95 is below the median of 138 across 633 observational studies indexed under Lymphoma.
Browse Lymphoma studies →Association for Training, Education, and Research in Hematology, Immunology, and Transplantation is the lead sponsor of 4 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Lymphoma patients will be recruited in on the French site
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Lymphoma Patients who are eligible will be included. Patients will undergo TEAM conditioning regimen followed by autologous haematopoietic stem cells transplantation according to standard practice of the centre and drugs label in France.
Progression free survival (PFS)
Time frame: 1 year after autologous haematopoietic stem cells transplantation
Overall Survival
Time frame: 100 days and at 1 year after autologous haematopoietic stem cells transplantation
Overall and complete response rate
Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation
Incidence of relapse
Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation
Impact of transplant-related mortality
Time frame: 100 days and 1 year after autologous haematopoietic stem cells transplantation
Incidence of infections
Time frame: during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation
Incidence of grade 3-4 side effects
Time frame: during aplasia, 100 days and 1 year after autologous haematopoietic stem cells transplantation
This study is completed, as verified in May 2020. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Association for Training, Education, and Research in Hematology, Immunology, and Transplantation