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在向新治疗时代过渡期间管理高危慢性淋巴细胞白血病:干细胞移植还是新型药物?

Managing high-risk CLL during transition to a new treatment era: stem cell transplantation or novel agents?

作者信息

Dreger Peter, Schetelig Johannes, Andersen Niels, Corradini Paolo, van Gelder Michel, Gribben John, Kimby Eva, Michallet Mauricette, Moreno Carol, Stilgenbauer Stephan, Montserrat Emili

机构信息

Department Medicine V, University of Heidelberg, Heidelberg, Germany;

Department Medicine I, University of Dresden, Dresden, Germany; German Bone Marrow Donor Registry, Tübingen, Germany;

出版信息

Blood. 2014 Dec 18;124(26):3841-9. doi: 10.1182/blood-2014-07-586826. Epub 2014 Oct 9.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) has been considered as the treatment of choice for patients with high-risk chronic lymphocytic leukemia (HR-CLL; ie, refractory to purine analogs, short response [<24 months] to chemoimmunotherapy, and/or presence of del[17p]/TP53 mutations). Currently, treatment algorithms for HR-CLL are being challenged by the introduction of novel classes of drugs. Among them, BCR signal inhibitors (BCRi) and B-cell lymphoma 2 antagonists (BCL2a) appear particularly promising. As a result of the growing body of favorable outcome data reported for BCRi/BCL2a, uncertainty is emerging on how to advise patients with HR-CLL about indication for and timing of HSCT. This article provides an overview of currently available evidence and theoretical considerations to guide this difficult decision process. Until the risks and benefits of different treatment strategies are settled, all patients with HR-CLL should be considered for treatment with BCRi/BCL2a. For patients who respond to these agents, there are 2 treatment possibilities: (1) performing an HSCT or (2) continuing treatment with the novel drug. Individual disease-specific and transplant-related risk factors, along with patient's preferences, should be taken into account when recommending one of these treatments over the other.

摘要

异基因造血干细胞移植(HSCT)已被视为高危慢性淋巴细胞白血病(HR-CLL,即对嘌呤类似物耐药、对化疗免疫疗法反应短暂[<24个月]和/或存在del[17p]/TP53突变)患者的首选治疗方法。目前,HR-CLL的治疗方案正受到新型药物引入的挑战。其中,BCR信号抑制剂(BCRi)和B细胞淋巴瘤2拮抗剂(BCL2a)似乎特别有前景。由于关于BCRi/BCL2a的有利结果数据越来越多,对于如何就HSCT的适应证和时机向HR-CLL患者提供建议,不确定性正在出现。本文概述了当前可用的证据和理论考量,以指导这一艰难的决策过程。在不同治疗策略的风险和益处确定之前,所有HR-CLL患者都应考虑使用BCRi/BCL2a进行治疗。对于对这些药物有反应的患者,有两种治疗选择:(1)进行HSCT或(2)继续使用新药治疗。在推荐这两种治疗方法中的一种时,应考虑个体疾病特异性和移植相关风险因素以及患者的偏好。

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