Outcomes of salvage haploidentical transplantation using posttransplant cyclophosphamide for graft failure following allogeneic hematopoietic stem cell transplantation.
Kaito HaradaYuho NajimaMotohiro KatoShigeo FujiAkihito ShinoharaHirohisa NakamaeMasako ToyosakiMiho AshiaraiMakoto OnizukaYoshiko HashiiTatsuo IchinoheYoshiko AtsutaHideki NakasonePublished in: International journal of hematology (2022)
Haploidentical donors have emerged as an alternative donor source for salvage stem cell transplantation (SCT) after graft failure; however, data regarding salvage haploidentical SCT using posttransplant cyclophosphamide (PTCy) are limited. Using nationwide data (2011-2019), we retrospectively investigated transplant outcomes after salvage haploidentical SCT using PTCy for graft failure (n = 33, median age 34 years). The total dose of PTCy was 75-100 mg/kg (standard dose) in 26 patients (78.8%) and 40-50 mg/kg (lower dose) in 5 patients (15.2%). The neutrophil engraftment rate at 30 days was 81.8%. One-year overall survival (OS) and non-relapse mortality (NRM) rates were 47.4% and 46.0%, respectively. The standard-dose group exhibited better OS (61.1% vs. 0.0% at 1 year, P = 0.022) and NRM (35.1% vs. 80.0% at 1 year, P = 0.052) than the lower-dose group. Moreover, the standard-dose group was less prone to both grades II-IV (11.5% vs. 40.0%) and III-IV (0.0% vs. 40.0%) acute graft-versus-host disease (GVHD). Use of cyclophosphamide in previous SCT and conditioning did not affect OS or NRM. In conclusion, haploidentical salvage SCT using PTCy offers promising survival outcomes. Prospective studies are required to validate the efficacy of salvage haploidentical SCT using PTCy.
Keyphrases
- stem cell transplantation
- high dose
- bone marrow
- end stage renal disease
- allogeneic hematopoietic stem cell transplantation
- peripheral blood
- low dose
- ejection fraction
- chronic kidney disease
- prognostic factors
- cord blood
- peritoneal dialysis
- acute lymphoblastic leukemia
- intensive care unit
- big data
- patient reported outcomes
- stem cells
- mesenchymal stem cells
- liver failure
- patient reported
- drug induced
- insulin resistance
- deep learning
- data analysis
- artificial intelligence
- glycemic control