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乳腺癌精准医学时代的优化生物标志物评估与分子检测

Optimized biomarker evaluation and molecular testing in the era of breast cancer precision medicine.

作者信息

Hicks David G, Turner Bradley M

机构信息

Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York, USA.

出版信息

Biotech Histochem. 2024 Oct;99(7):357-369. doi: 10.1080/10520295.2024.2390179. Epub 2024 Sep 11.

Abstract

Ground breaking advances in medicine, driven in part by major technologic developments in molecular biology have led us to a new model for cancer care that has been termed personalized, or precision medicine. Precision medicine is a model for making medical decisions that employs an innovative clinical approach and advanced tumor testing methods that are tailored to understanding an individual patient's tumor biology and the molecular drivers of their disease. This medical model includes a combination of diagnostic testing and specific treatment options that can be offered to patients at presentation and in theory throughout the course of their disease as new mutations arise with the development of disease recurrence. Although the precision medicine model offers incredible potential to transform cancer care, these advances are only meaningful when they reach the correct patients. The evolving paradigm of precision medicine is changing the practice of pathology, and the pathology community needs to be mindful of these changes because every tissue specimen represents a patient's life, and those patients are depending on the pathology community to handle their tissue correctly. The diagnostic tests performed in the pathology laboratory for precision medicine are increasingly complex, and pathologists along with the entire laboratory and clinical communities need to take steps to ensure that the right diagnosis is given to the right patient to inform the right treatment options, at the right time, along every step of the continuum of care for cancer patients. While hormone receptors and human epidermal growth factor receptor 2 (HER2) overexpression and/or amplification have been the mainstay for risk-stratification, and treatment decision making in breast cancer since the early 2000's, the seminal work on gene expression by Perou and colleagues in the early 2000's opened the door for molecular testing in the prognostic and predictive assessment of breast cancer. Molecular testing is now part of the standard of care in the precision medicine model for breast cancer care. In this article, the reader will gain a better understanding of how the lack of standardization of pre-analytic factors has the potential to negatively impact the quality of the tissue specimen for downstream biomarker and molecular testing, which ultimately can negatively affect patient care. The reader will also gain insight into the current climate surrounding molecular testing in breast cancer.

摘要

医学领域的突破性进展,部分是由分子生物学的重大技术发展推动的,这使我们走向了一种新的癌症治疗模式,即所谓的个性化或精准医学。精准医学是一种做出医疗决策的模式,它采用创新的临床方法和先进的肿瘤检测方法,旨在了解个体患者的肿瘤生物学特性及其疾病的分子驱动因素。这种医学模式包括诊断检测和特定的治疗方案,在患者就诊时以及理论上在其疾病的整个过程中,随着疾病复发出现新的突变时,都可以为患者提供这些方案。尽管精准医学模式为改变癌症治疗带来了巨大潜力,但这些进展只有应用于合适的患者时才有意义。精准医学不断演变的范式正在改变病理学的实践,病理学领域需要关注这些变化,因为每一个组织标本都代表着患者的生命,而这些患者依赖病理学领域正确处理他们的组织。病理实验室为精准医学进行的诊断检测越来越复杂,病理学家以及整个实验室和临床团队需要采取措施,确保在癌症患者连续护理的每一步,都能在正确的时间为正确的患者做出正确的诊断,以提供正确的治疗选择。自21世纪初以来,激素受体和人表皮生长因子受体2(HER2)的过表达和/或扩增一直是乳腺癌风险分层和治疗决策的主要依据,而21世纪初Perou及其同事关于基因表达的开创性工作为乳腺癌的预后和预测评估中的分子检测打开了大门。分子检测现在是乳腺癌精准医学治疗模式标准护理的一部分。在本文中,读者将更好地理解分析前因素缺乏标准化如何可能对下游生物标志物和分子检测的组织标本质量产生负面影响,最终可能对患者护理产生负面影响。读者还将深入了解当前乳腺癌分子检测的现状。

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