Title Effects of CD34(+) cell dose on haematopoietic recovery in acute lymphoblastic leukaemia patients with positive pretransplant measurable residual disease
Authors Wang, Yuewen
Mo, Xiaodong
Cheng, Yifei
Chen, Yuhong
Lv, Meng
Wang, Fengrong
Yan, Chenhua
Han, Wei
Chen, Huan
Xu, Lanping
Wang, Yu
Zhang, Xiaohui
Liu, Kaiyan
Huang, Xiaojun
Chang, Yingjun
Affiliation Peking Univ Peoples Hosp, Beijing, Peoples R China
Peking Univ, Inst Hematol, Natl Clin Res Ctr Hematol Dis, Beijing Key Lab Hematopoiet Stem Cell Transplanta, Beijing, Peoples R China
Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
Chinese Acad Med Sci, Res Unit Key Tech Diag & Treatments Hematol Malig, Beijing, Peoples R China
Keywords UNMANIPULATED HAPLOIDENTICAL BLOOD
ACUTE MYELOID-LEUKEMIA
UMBILICAL-CORD BLOOD
BONE-MARROW
POSTTRANSPLANTATION CYCLOPHOSPHAMIDE
PLATELET ENGRAFTMENT
PEDIATRIC-PATIENTS
CLINICAL-OUTCOMES
GRAFT COMPOSITION
TRANSPLANTATION
Issue Date Oct-2022
Publisher INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
Abstract Introduction A higher CD34(+) cell dose in allografts is associated with faster haematopoietic recovery after allogeneic haematopoietic stem cell transplantation (allo-HSCT). Leukaemia stem cells impair normal bone marrow (BM) niches and induce BM failure during leukemogenesis. However, whether measurable residual disease (MRD), known as the persistence of low-level leukaemic cells, could influence the effects of CD34(+) cell dose on haematopoietic recovery after transplantation in acute lymphoblastic leukaemia (ALL) patients is unknown. Methods A total of 975 ALL patients were enrolled and classified into pre-HSCT MRD-positive and MRD-negative subgroups. Cox proportional hazard regression models were built for time-to-event outcomes. Multivariate analysis was performed to determine independent influencing factors from the univariate analysis. Results An appropriate CD34(+) cell dose was positively associated with faster haematopoietic recovery in the total ALL population. More importantly, in pre-HSCT MRD-positive ALL patients, a higher CD34(+) cell dose (>= 2.76 x 10(6)/kg) was related to faster neutrophil (HR 1.330, 95% CI 1.045-1.692, p = 0.021) and platelet engraftment (HR 1.808, 95% CI 1.412-2.316, p < 0.001) in multivariate analysis. CD34(+) cell dose was a crucial factor associated with either engraftment or transplant outcomes, although we did not demonstrate direct correlations of CD34(+) cell dose with relapse, TRM, LFS or OS after allo-HSCT. Conclusion Our results indicated that no additional CD34(+) stem and progenitor cell harvests were needed to ensure successful haematopoietic recovery in pre-HSCT MRD-positive patients compared to pre-HSCT MRD-negative patients.
URI http://hdl.handle.net/20.500.11897/655680
ISSN 1751-5521
DOI 10.1111/ijlh.13974
Indexed SCI(E)
Appears in Collections: 人民医院

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