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风险分层指导下的供者淋巴细胞输注可降低异基因造血干细胞移植后标准风险急性白血病患者的复发率。

Risk stratification-directed donor lymphocyte infusion could reduce relapse of standard-risk acute leukemia patients after allogeneic hematopoietic stem cell transplantation.

机构信息

Peking University People's Hospital, Peking University Institute of Hematology, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, Peoples Republic of China.

出版信息

Blood. 2012 Apr 5;119(14):3256-62. doi: 10.1182/blood-2011-09-380386. Epub 2012 Feb 14.

DOI:10.1182/blood-2011-09-380386
PMID:22337715
Abstract

We studied the impact of risk stratification-directed interventions for minimal residual disease (MRD) on relapse and disease-free survival (DFS) prospectively in 814 subjects with standard-risk acute leukemia receiving allotransplantation in first or second complete remission. A total of 709 subjects were MRD(-) after transplantation (Group A); 105 subjects were MRD(+), 49 received low-dose IL-2 (Group B), and 56 received modified donor lymphocyte infusion (DLI) with or without low-dose IL-2 (Group C). Posttransplantation immune suppression for GVHD was also modified based on MRD state. The cumulative risk of relapse was significantly less and DFS was significantly better in subjects in Group C than in subjects in Group B (P = .001 and P = .002, respectively), but was not different from subjects in Group A (P = .269 and P = .688, respectively). Multivariate analyses confirmed that MRD state and modified DLI were significantly correlated with relapse (P = .000, odds ratio [OR] = 0.255 and P = .000, OR = 0.269) and DFS (P = .001, OR = 0.511 and P = .006, OR = 0.436, respectively). These data suggest that risk stratification-directed interventions with modified DLI in patients with standard-risk acute leukemia who are MRD(+) after transplantation may improve transplantation outcomes.

摘要

我们前瞻性地研究了在 814 例处于缓解期接受同种异体移植的标准风险急性白血病患者中,基于微小残留病(MRD)的危险分层指导干预对复发和无病生存(DFS)的影响。移植后共有 709 例患者 MRD(-)(A 组);105 例患者 MRD(+),49 例接受低剂量白细胞介素-2(IL-2)治疗(B 组),56 例接受改良供者淋巴细胞输注(DLI)联合或不联合低剂量 IL-2(C 组)。基于 MRD 状态,也对移植后移植物抗宿主病(GVHD)的免疫抑制进行了调整。与 B 组相比,C 组患者的复发风险明显降低,DFS 明显更好(P =.001 和 P =.002),但与 A 组无差异(P =.269 和 P =.688)。多变量分析证实,MRD 状态和改良 DLI 与复发(P =.000,优势比 [OR] = 0.255 和 P =.000,OR = 0.269)和 DFS(P =.001,OR = 0.511 和 P =.006,OR = 0.436)显著相关。这些数据表明,对于移植后 MRD(+)的标准风险急性白血病患者,基于危险分层的指导干预联合改良 DLI 可能改善移植结果。

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