Title Comparison of central nervous system relapse outcomes following haploidentical vs identical-sibling transplant for acute lymphoblastic leukemia
Authors Chen, Qi
Zhao, Xin
Fu, Hai-xia
Chen, Vu-hong
Zhang, Yuan-yuan
Wang, Jing-zhi
Wang, Yu
Yan, Chen-hua
Wang, Feng-rong
Mo, Xiao-dong
Han, Wei
Chen, Huan
Chang, Ying-jun
Xu, Lan-ping
Liu, Kai-yan
Huang, Xiao-jun
Zhang, Xiao-hui
Affiliation Peking Univ, Peoples Hosp, 11 Xizhimen South St, Beijing, Peoples R China
Peking Univ, Inst Hematol, Beijing, Peoples R China
Natl Clin Res Ctr Hematol Dis, Beijing, Peoples R China
Beijing Key Lab Hematopoiet Stem Cell Transplanta, Beijing, Peoples R China
Keywords STEM-CELL TRANSPLANTATION
BONE-MARROW-TRANSPLANTATION
ACUTE MYELOID-LEUKEMIA
UNRELATED CORD BLOOD
HIGH-RISK
EXTRAMEDULLARY RELAPSE
MISMATCHED HLA
ADULTS
CHEMOTHERAPY
MULTICENTER
Issue Date Jul-2020
Publisher ANNALS OF HEMATOLOGY
Abstract To explore the incidence, risk factors, and outcomes of central nervous system (CNS) relapse after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for acute lymphoblastic leukemia (ALL) and to compare the differences in CNS relapse between haploidentical donor HSCT (HID-HSCT) and HLA-identical sibling donor HSCT (ISD-HSCT). We performed a retrospective nested case-control study on patients with CNS relapse after allo-HSCT. The cumulative incidence of CNS relapse was 4.06% after allo-HSCT in ALL, with a significantly poor prognosis. The incidence was 3.91% and 5.36% in HID-HSCT and ISD-HSCT, respectively (p = .227). Among the patients with CNS relapse, the overall survival (OS) at 3 years was 56.2 +/- 6.8% in the HID-HSCT subgroup and 76.9 +/- 10.2% in the ISD-HSCT subgroup (p = .176). The 3-year cumulative incidence of systemic relapse was also comparable between the two subgroups (HID-HSCT, 40.6 +/- 7.4%; ISD-HSCT, 13.3 +/- 8.7%, respectively,p = .085). Younger age (p = .045), T-ALL (p = .035), hyperleukocytosis at diagnosis (p < .001), advanced disease stage at transplant (p < .001), pre-HSCT CNS involvement (p < .001), and absence of chronic graft vs host disease (cGVHD) (p < .001) were independent risk factors for CNS relapse after allo-HSCT. In conclusion, CNS relapse was a significant complication after allo-HSCT in ALL and was associated with poor prognosis. The incidences and outcomes were comparable between HID-HSCT and ISD-HSCT.
URI http://hdl.handle.net/20.500.11897/590102
ISSN 0939-5555
DOI 10.1007/s00277-020-04080-9
Indexed SCI(E)
Appears in Collections: 人民医院

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