Böttcher Sebastian
Division of Internal Medicine, Medical Clinic III-Hematology, Oncology and Palliative Medicine, Rostock University Medical Center, Rostock, Germany.
Methods Mol Biol. 2019;1956:157-197. doi: 10.1007/978-1-4939-9151-8_8.
The quantification of submicroscopic minimal residual disease (MRD) after therapy proved to have independent prognostic significance in many mature B-cell malignancies. With the advent of routine benchtop cytometers capable of simultaneously analyzing ≥4 colors and with improved standardization, flow cytometry has become the method of choice for MRD assessments in some lymphoma entities. Herein we describe general aspects of flow cytometric standardization. Chronic lymphocytic leukemia and multiple myeloma (MM) are used as examples to explain the technical standardization of flow cytometry for MRD detection according to EuroFlow strategies. MRD data acquisition and detailed analysis using a newly developed approach (so-called next generation flow, NGF) in MM is a particular focus of this chapter.
治疗后亚微观微小残留病(MRD)的定量在许多成熟B细胞恶性肿瘤中被证明具有独立的预后意义。随着能够同时分析≥4种颜色的常规台式细胞仪的出现以及标准化的改进,流式细胞术已成为某些淋巴瘤实体中MRD评估的首选方法。在此,我们描述流式细胞术标准化的一般方面。以慢性淋巴细胞白血病和多发性骨髓瘤(MM)为例,根据欧洲流式细胞术策略解释用于MRD检测的流式细胞术技术标准化。本章特别关注MM中使用新开发方法(所谓的新一代流式细胞术,NGF)进行的MRD数据采集和详细分析。