High-dose cytarabine chemotherapy (≥4 g/m2/day) before allogeneic hematopoietic stem cell transplantation for non-core-binding-factor AML in the first complete remission.
Yosuke NagahataTadakazu KondoYuichiro OnoNobuhiro HiramotoToshiyuki KitanoMasakatsu HishizawaKouhei YamashitaHisako HashimotoTakayuki IshikawaAkifumi Takaori-KondoPublished in: Leukemia & lymphoma (2020)
Benefit of high-dose cytarabine (HD-AraC) for acute myeloid leukemia (AML) prior to allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains unknown. We retrospectively analyzed data from 79 non-core-binding-factor AML patients who underwent allo-HSCT in their first complete remission (CR1). In univariate analysis, HD-AraC (≥4 g/m2/day) before allo-HSCT improved disease-free survival (DFS) (p = .018), overall survival (OS) (p = .029), and cumulative incidence of relapse (CIR) (p = .033). Four-year DFS, OS, and CIR of patients receiving and not receiving HD-AraC were 79% vs. 49%, 82% vs. 56%, and 18% vs. 42%, respectively. In multivariate analysis, HD-AraC was a positive prognostic factor for DFS (hazard ratio (HR) = 0.36, 95% confidence interval (CI): 0.14-0.88), OS (HR = 0.37, 95% CI: 0.14-0.99), and CIR (HR = 0.38, 95% CI; 0.14-1.0). Our study demonstrates that HD-AraC before allo-HSCT at a dose ≥4 g/m2/day is effective for treating AML patients in CR1.
Keyphrases
- acute myeloid leukemia
- allogeneic hematopoietic stem cell transplantation
- high dose
- prognostic factors
- free survival
- acute lymphoblastic leukemia
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- low dose
- hematopoietic stem cell
- stem cell transplantation
- patient reported outcomes
- risk factors
- squamous cell carcinoma
- systemic lupus erythematosus
- rheumatoid arthritis
- ulcerative colitis
- dna binding
- transcription factor