| Literature DB >> 34981143 |
Yibo Wu1,2,3,4, Yi Chen5, Panpan Zhu1,2,3,4, Baodong Ye6, Ying Lu7, Jimin Shi1,2,3,4, Yamin Tan8, Yanmin Zhao1,2,3,4, Jian Yu1,2,3,4, Xiaoyu Lai1,2,3,4, Jianping Lan9, Ting Si7, Lihong Ni10, He Huang1,2,3,4, Yi Luo11,12,13,14.
Abstract
Hepatitis B virus reactivation (HBVr) is not uncommon in allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients. Hepatitis B surface antigen (HBsAg)-positive patients receiving allo-HSCT have a very high risk of HBVr. However, the validity of prophylactic antiviral treatment in HBsAg-positive allo-HSCT recipients has not been well studied. We aimed to add experience in dealing with HBsAg-positive patients following allo-HSCT. We conducted a cohort study that included 11 years of data of HBsAg-positive allo-HSCT patients in multiple centers. The cumulative incidence of HBVr with antiviral prophylaxis at 60 months following transplantation was 8.9%. Both lamivudine (LAM) and entecavir (ETV) effectively reduced the incidence of HBVr. Patients with absent-mild cGVHD had a lower HBVr rate than that of patients with moderate-severe cGVHD (HR = 0.201, P = 0.020). The incidence of HBsAg seroclearance at 60 months following transplantation was 34.3%. Recipients accepting from anti-HBs-negative donors were associated with a lower HBsAg seroclearance rate than that of those accepting from anti-HBs-positive donors (HR=0.255, P < 0.001). The peripheral blood stem cell (PBSC) donor source had a higher HBsAg seroclearance rates than that of the PBSC plus bone marrow stem cell source (HR = 4.700, P = 0.047). The prophylactic antiviral treatment effectively reduced HBVr in HBsAg-positive recipients receiving allo-HSCT. HBsAg-positive recipients accept anti-HBs-positive PBSC donor sources may facilitate the acquisition of HBsAg seroclearance after transplantation.Entities:
Keywords: HBV reactivation; HBsAg-positive; Hematopoietic stem transplantation; Hepatitis B virus; Prophylactic antiviral treatment
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Year: 2022 PMID: 34981143 DOI: 10.1007/s00277-021-04730-6
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673