Kern Wolfgang, Kohlmann Alexander, Schnittger Susanne, Hiddemann Wolfgang, Schoch Claudia, Haferlach Torsten
Laboratory for Leukemia Diagnostics, Department of Internal Medicine III, University Hospital Grosshadern, Munich, Germany.
Am J Pharmacogenomics. 2004;4(4):225-37. doi: 10.2165/00129785-200404040-00002.
The standard methods for establishing the diagnosis of acute leukemias are cytomorphology and cytochemistry in combination with multiparameter immunophenotyping. Cytogenetics, fluorescence in situ hybridization, and PCR-based assays add important information regarding biologically defined and prognostically relevant subgroups, and allow a comprehensive diagnosis of well-defined subentities. In the clinical setting, a better understanding of the clinical course of distinct, biologically defined disease subtypes is the basis for a selection of disease-specific therapeutic approaches. As knowledge of deregulated pathways in leukemia increases and accelerates the development of new therapeutics, a detailed and comprehensive diagnostic tool is required. Microarray technology, which quantifies gene expression intensities of thousands of genes in a single analysis, has the potential to become an essential tool for the molecular classification of leukemias. It may, therefore, be used as a routine method for diagnostic purposes in the near future. Furthermore, gene expression profiling may also lead to the detection of new biologically defined and clinically relevant subtypes in leukemia and guide therapeutic decision-making in the future.
诊断急性白血病的标准方法是细胞形态学和细胞化学结合多参数免疫表型分析。细胞遗传学、荧光原位杂交和基于聚合酶链反应的检测可提供有关生物学定义和预后相关亚组的重要信息,并有助于对明确的亚实体进行全面诊断。在临床环境中,更好地了解不同生物学定义的疾病亚型的临床病程是选择疾病特异性治疗方法的基础。随着白血病中失调通路知识的增加并加速新疗法的开发,需要一种详细而全面的诊断工具。微阵列技术可在单次分析中对数千个基因的表达强度进行定量,有潜力成为白血病分子分类的重要工具。因此,在不久的将来它可能会用作诊断目的的常规方法。此外,基因表达谱分析还可能导致在白血病中检测出新的生物学定义和临床相关亚型,并在未来指导治疗决策。