| Literature DB >> 33389025 |
Qi Chen1,2,3,4, Xiao-Lu Zhu1,2,3,4, Xin Zhao1,2,3,4, Xiao Liu1,2,3,4, Hai-Xia Fu1,2,3,4, Yuan-Yuan Zhang1,2,3,4, Yu-Hong Chen1,2,3,4, Xiao-Dong Mo1,2,3,4, Wei Han1,2,3,4, Huan Chen1,2,3,4, Chen-Hua Yan1,2,3,4, Yu Wang1,2,3,4, Ying-Jun Chang1,2,3,4, Lan-Ping Xu1,2,3,4, Xiao-Jun Huang1,2,3,4, Xiao-Hui Zhang1,2,3,4.
Abstract
We performed a nested case-control study to investigate the incidence, treatment, and prognosis of central nervous system (CNS) relapse after allogenic hematopoietic stem cell transplantation (allo-HSCT) for acute myeloid leukemia (AML) and compared the outcomes of patients with CNS relapse following haploidentical donor (HID) HSCT versus identical sibling donor (ISD) HSCT. A total of 37 patients (HID-HSCT, 24; ISD-HSCT, 13) developed CNS relapse after transplantation between January 2009 and January 2019, with an incidence of 1.81%. The median time from transplantation to CNS relapse was 239 days. Pre-HSCT CNS involvement (HR 6.940, 95% CI 3.146-15.306, p < .001) was an independent risk factor for CNS relapse after allo-HSCT for AML. The 3-year overall survival (OS) for patients with CNS relapse was 60.3 ± 8.8%, which was significantly lower than that in the controls (81.5 ± 4.5%, p = .003). The incidence of CNS relapse was 1.64% for patients who received HID-HSCT and 2.55% for those who received ISD-HSCT (p = .193). There was no significant difference in OS between the HID-HSCT and ISD-HSCT subgroups among the patients with CNS relapse. In conclusion, CNS relapse is a rare but serious complication after allo-HSCT for AML, and the incidence and outcomes of patients with CNS relapse are comparable following HID-HSCT and ISD-HSCT.Entities:
Keywords: Acute myeloid leukemia; Allogenic hematopoietic stem cell transplantation; Central nervous system; Prognosis; Relapse
Year: 2021 PMID: 33389025 DOI: 10.1007/s00277-020-04380-0
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673