Abstract

G-CSF-mobilized peripheral blood (G-PB) harvest is the predominant graft for identical sibling donor and unrelated donor allogeneic hematopoietic stem cell transplantation (HSCT) recipients, but it was controversial in haploidentical related donor (HID) HSCT. In this registry study, we aimed to identify the efficacy of HID G-PB HSCT (HID-PBSCT) for acute leukemia (AL) patients in first complete remission (CR1). Also, we reported the outcomes for the use of G-PB grafts in comparison with the combination of G-BM and G-PB grafts in HID HSCT recipients. Sixty-seven AL patients in CR1 who received HID-PBSCT were recruited at Institute of Hematology, Peking University. Patients who received haploidentical HSCT using the combination of G-BM and G-PB harvests in the same period were enrolled as controls (n=392). The median time from HSCT to neutrophil and platelet engraftment was 12 days (range, 9–19 days) and 12 days (range, 8–171 days), respectively. The 28-day cumulative incidence of neutrophil and platelet engraftment after HSCT was 98.5% and 95.5%, respectively. The cumulative incidences of grade II–IV and grade III–IV acute graft-versus-host disease (GVHD) were 29.9% (95%CI 18.8–40.9%) and 7.5% (95%CI 1.1–13.8%), respectively. The cumulative incidences of total and moderate-severe chronic GVHD were 54.9% (95%CI 40.9–68.8%) and 17.4% (95%CI 6.7–28.0%), respectively. The cumulative incidences of relapse and non-relapse mortality were 13.9% (95%CI 5.4–22.5%) and 3.4% (95%CI 0–8.1%), respectively. The probabilities of overall survival (OS) and leukemia-free survival (LFS) were 84.7% (95%CI 74.7–94.7%) and 82.7% (95%CI 73.3–92.1%) respectively. Compared with the HID HSCT recipients using the combination of G-BM and G-PB grafts, the engraftments of neutrophil and platelet were both significantly faster for the G-PB group, and the other clinical outcomes were all comparable between the groups. In multivariate analysis, graft types did not influence the clinical outcomes. Overall, for the patients with AL CR1, G-PB graft could be considered an acceptable graft for HID HSCT recipients. This study was registered at https://clinicaltrials.gov as NCT03756675.

Highlights

  • Allogeneic hematopoietic stem cell transplantation is the most important curative option for patients with acute leukemia (AL)

  • This study indicated that hematopoietic recovery for those using GPB grafts was faster compared with those using G-bone marrow (BM) plus G-peripheral blood (PB) grafts, and GVHD, relapse, non-relapse mortality (NRM), and survivals were similar between groups

  • This study provided an opportunity for exploring the up-to-date undefined role of Haploidentical related donors (HIDs) PBSC transplantation (PBSCT) in AL CR1 patients with the antithymocyte globulin (ATG)-based regimen

Read more

Summary

Introduction

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the most important curative option for patients with acute leukemia (AL). The graft was one of the critical factors for allo-HSCT. Many studies had compared the clinical outcomes between patients using PB and BM grafts. In patients with human leukocyte antigen identical sibling donors (ISDs), engraftment was faster [1,2,3], the relapse rate was lower [4], and the leukemia-free survival (LFS) rate was better in the PB group compared with the BM group, for the patients with advanced stage disease [1, 4]. In the HID HSCT regimen using post-transplant cyclophosphamide (PTCY), several prospective studies compared the clinical outcomes between PB grafts and BM grafts. Engraftment was significantly faster in the PB group; but the difference of the GVHD rates between PB and BM groups was not as significant as those of ISD and URD HSCT recipients. Some studies observed that the LFS rates were significantly poorer in the PB group compared with BM group [8,9,10]; the other studies observed that LFS rates of PB group were better than those of BM group [11,12,13]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call