Affiliation:
1. The First Affiliated Hospital, Zhejiang University School of Medicine
2. The First Affiliated Hospital, School of Medicine, Zhejiang University
3. First affiliated hospital of Zhejiang university school of medicine
4. The First Affiliated Hospital,School of Medicine, Zhejiang University
Abstract
Abstract
During hematopoietic stem cell transplantation (HSCT), ATG depletes T cells in-vivo to improve engraftment and prevent graft-versus-host disease (GVHD). Here, we compared the clinical efficacy of two different types of ATGs: thymoglobulin and anti-human T-lymphocyte immunoglobulin (Grafalon). A total of 469 patients who received haploidentical transplantation were enrolled in this study. After a propensity score (PS)-matched analysis, 209 patients were assigned to each group. Primary outcome was overall survival (OS). There was no significant difference in OS between two groups. Within the first 180 days after HSCT, Grafalon was associated with lower incidences of Epstein-Barr virus (EBV) viremia (31.6 vs 54.5%, P < 0.0001) and cytomegalovirus viremia (CMV) viremia (54.5 vs 67.9%, P = 0.005) compared to thymoglobulin. Patients receiving Grafalon had a higher rate of moderate/severe chronic GVHD (26.3 vs 18.2%, P = 0.046). However, the incidences of engraftment failure, grade II-IV acute GVHD, relapse, non-relapse mortality (NRM) and GVHD-free relapse-free survival (GRFS) did not differ greatly between groups. In the subgroup analysis, Grafalon improved the OS of lymphoid malignancies with young ages (< 40 years old) (HR, 0.55; P = 0.04) or with a high/very high disease risk index (HR, 0.36; P = 0.04). In conclusion, our results suggest the two types of ATG may differentially influence transplant outcomes.
Publisher
Research Square Platform LLC