乳腺癌的药物诊断试验:关注HER2和曲妥珠单抗治疗

John M S Bartlett
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引用次数: 21

摘要

药物基因组学被定义为对遗传基因变异的研究,遗传变异决定了个体对治疗药物的反应。在肿瘤学领域,基于后续癌细胞世代遗传的体细胞分子改变的药物基因组学形成了新治疗剂分子靶向的基础。从这些药物的临床经验来看,需要适当的药物诊断方法来确保药物正确靶向。鉴于目前正在评估的用于癌症治疗的药物基因组学药物范围广泛,似乎在未来5-10年(如果不是更早的话)将需要快速扩展药物诊断分析。如果成功实现这一目标,过去的经验教训,特别是在开发HER2 (ERBB2)检测以指导曲妥珠单抗治疗乳腺癌的过程中,可能为未来药物诊断检测系统的开发提供一个有价值的框架。本文回顾了曲妥珠单抗靶向乳腺癌的生物学和临床基础,以及验证和改进检测肿瘤HER2蛋白表达和HER2基因扩增的药物诊断程序所采取的步骤。关注的是测试方法的质量保证和可重复性,以及曲妥珠单抗应答患者的最佳选择。这种方法为肿瘤学药物诊断试验的未来发展提供了范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacodiagnostic testing in breast cancer: focus on HER2 and trastuzumab therapy.

Pharmacogenomics is defined as research into inherited genetic variations that determine an individual's response to therapeutic agents. In oncology, pharmacogenomics based on somatic molecular alterations inherited by subsequent cancer cell generations forms the basis of molecular targeting of novel therapeutic agents. What has emerged from clinical experience with such agents is the need for appropriate pharmacodiagnostic approaches to ensure the drugs are correctly targeted. Given the broad range of pharmacogenomic agents currently under evaluation for cancer therapy, it appears that a rapid extension of pharmacodiagnostic profiling will be required in the next 5-10 years, if not sooner. If this is to be successfully achieved, lessons learned in the past, particularly during the development of HER2 (ERBB2) testing for directing trastuzumab therapy in breast cancer, may provide a valuable framework for the development of future pharmacodiagnostic assays system. This article reviews the biological and clinical rationale for targeting breast cancer with trastuzumab and the steps taken to validate and improve pharmacodiagnostic procedures for testing tumor HER2 protein expression and HER2 gene amplification. Attention is given to quality assurance and reproducibility of testing approaches and the optimal selection of patients for response to trastuzumab. This approach serves as a paradigm for the future development of pharmacodiagnostic tests in oncology.

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