a Department of Hematology , Ion Chiricuta Clinical Cancer Center , Cluj Napoca , Romania.
b Research Center for Functional Genomics and Translational Medicine/Hematology , Iuliu Hatieganu University of Medicine and Pharmacy , Cluj Napoca , Romania.
Crit Rev Clin Lab Sci. 2018 Aug;55(5):329-345. doi: 10.1080/10408363.2018.1463508. Epub 2018 May 25.
Chronic lymphocytic leukemia (CLL) is a malignancy defined by the accumulation of mature lymphocytes in the lymphoid tissues, bone marrow, and blood. Therapy for CLL is guided according to the Rai and Binet staging systems. Nevertheless, state-of-the-art protocols in disease monitoring, diagnostics, and prognostics for CLL are based on the assessment of minimal residual disease (MRD). MRD is internationally considered to be the level of disease that can be detected by sensitive techniques and represents incomplete treatment and a probability of disease relapse. MRD detection has been continuously improved by the quick development of both flow cytometry and molecular biology technology, as well as by next-generation sequencing. Considering that MRD detection is moving more and more from research to clinical practice, where it can be an independent prognostic marker, in this paper, we present the methodologies by which MRD is evaluated, from translational research to clinical practice.
慢性淋巴细胞白血病(CLL)是一种以淋巴组织、骨髓和血液中成熟淋巴细胞积累为特征的恶性肿瘤。CLL 的治疗是根据 Rai 和 Binet 分期系统进行指导的。然而,CLL 的疾病监测、诊断和预后的最新方案是基于微小残留病(MRD)的评估。MRD 被国际上认为是可以通过敏感技术检测到的疾病水平,代表治疗不完全和疾病复发的概率。随着流式细胞术和分子生物学技术的快速发展以及下一代测序技术的发展,MRD 的检测不断得到改进。鉴于 MRD 检测越来越从研究转移到临床实践,并且可以作为独立的预后标志物,在本文中,我们介绍了从转化研究到临床实践中评估 MRD 的方法。