Panuzzo Cristina, Jovanovski Aleksandar, Ali Muhammad Shahzad, Cilloni Daniela, Pergolizzi Barbara
Department of Clinical and Biological Sciences, University of Turin, 10124 Turin, Italy.
J Clin Med. 2022 Jan 18;11(3):483. doi: 10.3390/jcm11030483.
The efforts made in the last decade regarding the molecular landscape of acute myeloid leukemia (AML) have created the possibility of obtaining patients' personalized treatment. Indeed, the improvement of accurate diagnosis and precise assessment of minimal residual disease (MRD) increased the number of new markers suitable for novel and targeted therapies. This progress was obtained thanks to the development of molecular techniques starting with real-time quantitative PCR (Rt-qPCR) passing through digital droplet PCR (ddPCR) and next-generation sequencing (NGS) up to the new attractive metabolomic approach. The objective of this surge in technological advances is a better delineation of AML clonal heterogeneity, monitoring patients without disease-specific mutation and designing customized post-remission strategies based on MRD assessment. In this context, metabolomics, which pertains to overall small molecules profiling, emerged as relevant access for risk stratification and targeted therapies improvement. In this review, we performed a detailed overview of the most popular modern methods used in hematological laboratories, pointing out their vital importance for MRD monitoring in order to improve overall survival, early detection of possible relapses and treatment efficacy.
过去十年间,在急性髓系白血病(AML)分子格局方面所做的努力为实现患者的个性化治疗创造了可能。事实上,准确诊断的改进以及微小残留病(MRD)的精确评估增加了适用于新型靶向治疗的新标志物数量。这一进展得益于分子技术的发展,从实时定量聚合酶链反应(Rt-qPCR)开始,历经数字液滴聚合酶链反应(ddPCR)和下一代测序(NGS),直至新兴的有吸引力的代谢组学方法。技术进步激增的目标是更好地描绘AML的克隆异质性,监测无疾病特异性突变的患者,并基于MRD评估设计定制的缓解后策略。在此背景下,代谢组学涉及整体小分子谱分析,成为风险分层和改善靶向治疗的相关途径。在本综述中,我们对血液学实验室中使用的最流行的现代方法进行了详细概述,指出它们对MRD监测的至关重要性,以提高总生存率、早期发现可能的复发以及治疗效果。