Low-dose post-transplant cyclophosphamide with low-dose antithymocyte globulin for prevention of graft-versus-host disease in first complete remission undergoing 10/10 HLA-matched unrelated donor peripheral blood stem cell transplants: a multicentre, randomized controlled trial.
Yingling ZuZhen LiRuirui GuiYanyan LiuYanli ZhangFengkuan YuHuifang ZhaoYuewen FuXinrong ZhanZhongliang WangPengtao XingXianjing WangHuili WangJian ZhouYong-Ping SongPublished in: Bone marrow transplantation (2022)
The most widely used regimens of graft-versus-host disease (GVHD) prophylaxis in HLA-matched unrelated donor peripheral blood stem cell transplantation (MUD-PBSCT) are based on anti-thymocyte globulin (ATG) or post-transplant cyclophosphamide (PTCy). To improve the efficiency of GVHD prophylaxis, a novel regimen, composed of low-dose PTCy (20 mg/kg on day +3 and +4) and low-dose ATG (6 mg/kg), was evaluted in patients with hematological malignancies ungoing 10/10 HLA MUD-PBSCT in first remission (CR1). In our prospective, multicenter study, 104 patients were randomly assigned one-to-one to low-dose PTCy-ATG (n = 53) or standard-dose ATG (10 mg/kg, n = 51). Both the cumulative incidences (CIs) of grade II-IV acute GVHD (aGVHD) and chronic GVHD (cGVHD) at 2 years in low-dose PTCy-ATG cohort were significantly reduced (24.5% vs. 47.1%; P = 0.017; 14.1% vs. 33.3%; P = 0.013). The CI of non-relapse-mortality (NRM) was much lower (13.2% vs. 34.5%; P = 0.049) and GVHD-free, relapse-free survival (GRFS) was significantly improved at 2 years in low-dose PTCy-ATG arm (67.3% vs 42.3%; P = 0.032). The low-dose PTCy-ATG based GVHD prophylaxis is a promising strategy for patients in CR1 after 10/10 HLA MUD-PBSCT.
Keyphrases
- low dose
- high dose
- stem cell transplantation
- peripheral blood
- randomized controlled trial
- free survival
- end stage renal disease
- allogeneic hematopoietic stem cell transplantation
- stem cells
- ejection fraction
- chronic kidney disease
- newly diagnosed
- prognostic factors
- clinical trial
- systematic review
- cardiovascular disease
- study protocol
- type diabetes
- hepatitis b virus
- acute myeloid leukemia
- liver failure
- mesenchymal stem cells
- bone marrow
- cross sectional
- drug induced
- patient reported outcomes
- acute respiratory distress syndrome
- meta analyses