BeEAM Versus CEM in Lymphoma Patients as a Conditioning Regimen Before Autologous Hematopoietic Cell Transplantation
Lymphoma

About this trial
This is an interventional treatment trial for Lymphoma
Eligibility Criteria
Inclusion Criteria 1. Patients with lymphoma relapsed/refractory (RR) Hodgkin's lymphoma (HL) and non-Hodgkin lymphoma (NHL) with all subtypes. 2. Treat with conventional dose salvage regimens 3. Remission status before HSCT is complete remission (CR) or partial remission (PR). 4. Age>18 years. 5. Gender male and female. 6. CD34+ count cells <2 ×106 CD34+ cells/kg BW. Exclusion Criteria Remission status before HSCT is non remission (NR) or progressive disease (PD). CD34+ count cells <2 ×106 CD34+ cells/kg BW CNS lymphoma or solid tumor not included in population. Pregnancy or breast-feeding. Any Psychological, familial, sociological, or geographical factor that interfere with patient adherence to medications. History of allergy to any medications in both protocol
Sites / Locations
- International Medical Center (IMC) Hospital, Cairo, Egypt.
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
BeEAM Regimen
CEM Regimen
BeEAM (Bendamustine, Etoposide, Cytarabine, Melphalan)
CEM (Carboplatin, Etoposide, Melphalan)