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定量微小残留病监测可识别慢性淋巴细胞白血病异基因干细胞移植后的不同移植物抗白血病反应模式:来自GCLLSG CLL3X试验的结果。

Quantitative MRD monitoring identifies distinct GVL response patterns after allogeneic stem cell transplantation for chronic lymphocytic leukemia: results from the GCLLSG CLL3X trial.

作者信息

Ritgen M, Böttcher S, Stilgenbauer S, Bunjes D, Schubert J, Cohen S, Humpe A, Hallek M, Kneba M, Schmitz N, Döhner H, Dreger P

机构信息

Department of Medicine II, University of Schleswig-Holstein, Kiel, Germany.

出版信息

Leukemia. 2008 Jul;22(7):1377-86. doi: 10.1038/leu.2008.96. Epub 2008 Apr 17.

Abstract

The purpose of this study was to prospectively analyze minimal residual disease(MRD) kinetics after reduced-intensity allogeneic stem cell transplantation (allo-SCT) in high-risk chronic lymphocytic leukemia (CLL). Subjects were the first 30 consecutive patients from a prospective clinical trial, and seven pilot patients treated identically. Using real-time quantitative-PCR (RQ-PCR) and/or flow-based MRD monitoring (sensitivity >or=10(-4)), five distinct patterns of MRD kinetics could be identified: patients who promptly achieved durable MRD negativity without direct evidence of graft-versus-leukemia (GVL) effects (Group 1) (n=4; no clinical relapse); patients with complete and sustained MRD response after GVL induced by immunosuppression tapering (Group 2) or donor lymphocyte infusions (Group 3) (n=18; one relapse); patients without MRD response due to lack of GVL (Group 4) (n=2; two relapses); patients with incomplete and transient MRD response to GVL (Group 5) (n=4; three relapses). In summary, this study provides a comprehensive map of possible MRD courses and their prognostic implications after T-replete allo-SCT in high-risk CLL, indicating that effective GVL activity is induced virtually in all patients who develop chronic GVHD. However, in a significant proportion of cases, this does not translate into sustained disease control due to development of secondary GVL resistance.

摘要

本研究的目的是前瞻性分析高危慢性淋巴细胞白血病(CLL)患者接受减低强度异基因干细胞移植(allo-SCT)后的微小残留病(MRD)动力学。研究对象为一项前瞻性临床试验中的前30例连续患者,以及7例接受相同治疗的试点患者。使用实时定量聚合酶链反应(RQ-PCR)和/或基于流式细胞术的MRD监测(灵敏度≥10⁻⁴),可识别出5种不同的MRD动力学模式:在无移植物抗白血病(GVL)效应直接证据的情况下迅速实现持久MRD阴性的患者(第1组)(n = 4;无临床复发);在免疫抑制逐渐减量(第2组)或供体淋巴细胞输注(第3组)诱导GVL后实现完全且持续MRD缓解的患者(n = 18;1例复发);因缺乏GVL而无MRD缓解的患者(第4组)(n = 2;2例复发);对GVL有不完全且短暂MRD缓解的患者(第5组)(n = 4;3例复发)。总之,本研究提供了高危CLL患者接受T细胞充足的allo-SCT后可能的MRD病程及其预后意义的全面图谱,表明几乎所有发生慢性移植物抗宿主病(GVHD)的患者均诱导出有效的GVL活性。然而,在相当一部分病例中,由于继发性GVL耐药的发生,这并未转化为持续的疾病控制。

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