Posttransplant cyclophosphamide in unrelated and related peripheral blood stem cell transplantation from HLA-matched and 1 allele mismatched donor.
Junichi SugitaTakashi KurohaJun IshikawaTetsuya EtoKentaro FukushimaIsao YokotaKoichi AkashiShuichi TaniguchiMine HaradaTakanori TeshimaPublished in: Bone marrow transplantation (2023)
Posttransplant cyclophosphamide (PTCy)-based graft-versus-host disease (GVHD) prophylaxis has been increasingly used in HLA-haploidentical transplantation and recent studies also demonstrated the efficacy of PTCy in HLA-matched transplantation. We conducted a prospective multicenter phase II study to evaluate the safety and efficacy of PTCy with tacrolimus and mycophenolate mofetil in 43 patients who underwent HLA-matched (n = 21), 1 allele mismatched (n = 20), or 2 allele mismatched (n = 2) peripheral blood stem cell transplantation (PBSCT) following myeloablative (n = 28) or reduced-intensity (n = 15) conditioning. The incidence of grade III-IV acute GVHD at 100 days was 2.3%. The incidences of grades II-IV acute GVHD, all grade chronic GVHD, and moderate to severe chronic GVHD at 2 years were 16.3%, 14.0%, and 4.7%, respectively. Overall survival, disease-free survival, and non-relapse mortality at 2 years were 75.3%, 74.0%, and 7.0%, respectively. GVHD-free, relapse-free survival at 2 years was 67.0%. The rate of off-immunosuppressants in patients who survived without relapse at 2 years was 85.4%. These results indicate that PTCy is a valid option for GVHD prophylaxis in both HLA-matched and HLA 1-2 allele mismatched PBSCT.
Keyphrases
- free survival
- stem cell transplantation
- high dose
- allogeneic hematopoietic stem cell transplantation
- peripheral blood
- phase ii study
- low dose
- drug induced
- liver failure
- end stage renal disease
- acute lymphoblastic leukemia
- respiratory failure
- chronic kidney disease
- risk factors
- high intensity
- stem cells
- ejection fraction
- newly diagnosed
- randomized controlled trial
- cardiovascular disease
- cell therapy
- type diabetes
- bone marrow
- clinical trial
- coronary artery disease
- open label
- peritoneal dialysis
- cross sectional
- hepatitis b virus
- cardiovascular events
- cord blood