Allogeneic stem cell transplantation and CAR-T in B-cell Non-Hodgkin Lymphoma: a two-center experience and review of the literature.
Santiago MercadalAlberto MussettiCatherine J LeeCarolina ArevaloSilvina M OdstrcilEsteban PeñaAnna SuredaDaniel R CourielPublished in: Annals of hematology (2024)
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is still a potentially curative option for B-cell Non-Hodgkin Lymphoma (B-NHL) in the modern immunotherapy era. The objective of this study was to analyze long-term outcomes of patients with B-NHL who received allo-HSCT. We analyzed overall survival (OS), progression-free survival (PFS) and graft versus host disease (GVHD) relapse-free survival (GRFS) in 53 patients undergoing allo-HSCT from two institutions. The median follow-up of the study was 72 months (range 29-115 months). The median number of lines of therapy before allo-HSCT was 3 (range 1-6) and twenty-eight patients (53%) had received a previous autologous transplant. The 3-year PFS, OS and GRFS were 55%, 63%, and 55%, respectively. One-year non-relapse mortality was 26%. Karnofsky Performance Scale < 90 was associated with worse OS in multivariable analysis. A non-comparative analysis of a cohort of 44 patients with similar characteristics who received chimeric antigen receptor T-cell therapy was done, showing a 1-year PFS and OS were 60% and 66%, respectively. Our data shows that allo-HSCT is still a useful option for treating selected patients with R/R B-NHL. Our retrospective analysis and review of the literature demonstrate that allo-HSCT can provide durable remissions in a subset of patients with R/R B-NHL.
Keyphrases
- free survival
- hematopoietic stem cell
- stem cell transplantation
- cell therapy
- allogeneic hematopoietic stem cell transplantation
- patients undergoing
- high dose
- end stage renal disease
- acute lymphoblastic leukemia
- stem cells
- prognostic factors
- chronic kidney disease
- ejection fraction
- bone marrow
- peritoneal dialysis
- low dose
- rectal cancer
- big data