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

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 af