Upfront allogeneic hematopoietic stem cell transplantation for adult T-cell acute lymphoblastic leukemia/lymphoma in first complete remission: a single-center study

被引:0
|
作者
Gu, Zhenyang [1 ]
Li, Fei [1 ]
Li, Meng [1 ]
Wang, Lu [1 ]
Lu, Ning [1 ]
Jin, Xiangshu [1 ]
Wang, Lili [1 ]
Gao, Chunji [1 ]
Dou, Liping [1 ]
Liu, Daihong [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Hematol, East St 8th, Beijing 100071, Peoples R China
基金
中国国家自然科学基金;
关键词
T-cell acute lymphoblastic leukemia/lymphoma; Allogeneic stem cell transplantation; Antithymocyte globulin; Upfront; CR1; MINIMAL RESIDUAL DISEASE; LEUKEMIA; RISK; RELAPSE; BLOOD;
D O I
10.1007/s00277-024-05716-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Real-world data on outcomes of upfront allogeneic hematopoietic stem cell transplantation (allo-HCT) for adult T-cell acute lymphoblastic leukemia/lymphoma (T-ALL) patients in first complete remission (CR1) is still lacking. Methods: A single center retrospective study was conducted from 94 consecutive patients received their first allo-HCT between 2010 and 2021, which include 76 patients received upfront allo-HCT and 18 patients received allo-HCT in non-upfront settings. Results: There were no significant differences in most variables. In the upfront allo-HCT group, 52 (68%) patients achieved CR1 with one cycle of induction regimen. 24 (32%) patients achieved CR1 with more than one cycle. In the non-upfront group, there were 14 patients with active disease and 4 patients in second CR before transplant. The majority of patients received antithymocyte globulin-based graft-versus-host disease prophylaxis. Median follow-up time was 51 months for both groups. 5-year overall survival (OS) was 54% in the upfront allo-HCT group. While, in the non-upfront group, 5-year OS were 19% (P = 0.013). 5-year progression free survival in the upfront group was higher than that in the non-upfront group (50% versus 20%, P = 0.02). 5-year cumulative incidence relapse rate was significantly higher in non-upfront group (64% vs. 32%, P = 0.006). While, there was no difference in the 5-year non-relapse mortality (NRM) rate (19% versus 16%, P = 0.56). The most common cause of death was disease progression. In multivariable analysis, non-upfront allo-HCT (hazard ratios (HR) 2.14, P = 0.03) and HCT-CI (>= 2) (HR 6.07, P = 0.002) were identified to be associated with worse OS. Non-upfront allo-HCT and HCT-CI (>= 2) were also found to be independent risk factors for higher relapse rate. While, haploidentical-HCT was found to be associated with increased NRM. Conclusions: Our study indicated that allo-HCT remains an important curative treatment for adult patients with T-ALL, especially when it was performed in the upfront setting.
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收藏
页码:2445 / 2454
页数:10
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