Rituximab added to conditioning regimen significantly improves erythroid engraftment in major incompatible ABO-group hematopoietic stem cell transplantation.
Maria Chiara FinazziAlessandra WeberChiara PavoniAnna GrassiMaria Caterina MicòAlessandra AlgarottiFederico LussanaAlessandro RambaldiPublished in: Bone marrow transplantation (2024)
ABO-group major incompatibility hematopoietic stem cell transplantation (HSCT) increases the risk of delayed red cell engraftment and other immunological complications. In this study, we evaluated the efficacy of pre-transplant infusion of rituximab in patients with ABO-incompatibility in improving red blood cell engraftment after HSCT, measured by time to reach transfusion independence. We performed a retrospective, single-center study including 131 consecutive patients transplanted with major or bidirectional ABO-incompatible grafts between 1st January 2013 and 31st December 2019. Fifty-one patients received an infusion of rituximab during the conditioning regimen, while 80 patients did not receive any additional preventive treatment. Time to transfusion independence was significantly reduced for patients treated with rituximab (1 month, 95% CI, 0.5-2) compared with the control group (3.2 months, 95% CI 1.5-3.2, p = 0.02). By multivariable analysis, rituximab use was associated with a faster red blood cell (RBC) engraftment (RR 1.88, 95% CI 1.17-3.03, p = 0.009), while a pre-transplant anti-donor isohemagglutinins titer >1:128 was associated with delayed transfusion independence (RR 0.61, 95% CI 0.37-0.99, p = 0.05). Although limited by the retrospective nature of the study, the results of this analysis suggest that rituximab added to conditioning regimens is feasible, safe, and able to improve post-transplant red blood cell engraftment.
Keyphrases
- red blood cell
- end stage renal disease
- diffuse large b cell lymphoma
- ejection fraction
- chronic kidney disease
- newly diagnosed
- prognostic factors
- cardiac surgery
- hematopoietic stem cell
- hodgkin lymphoma
- low dose
- acute myeloid leukemia
- patient reported outcomes
- cross sectional
- risk factors
- smoking cessation
- sickle cell disease