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癌症个体化医学中药物基因组学引入的挑战和误区。

Challenges and pitfalls in the introduction of pharmacogenetics for cancer.

机构信息

Cancer Science Institute of Singapore, National University of Singapore, Singapore.

出版信息

Ann Acad Med Singap. 2011 Aug;40(8):369-74.

Abstract

There have been several success stories in the field of pharmacogenetics in recent years, including the analysis of HER2 amplification for trastuzumab selection in breast cancer and VKORC1 genotyping for warfarin dosing in thrombosis. Encouraging results from these studies suggest that genetic factors may indeed be important determinants of drug response and toxicity for at least some drugs. However, to apply pharmacogenetics appropriately, a thorough understanding of the scope and limitations of this field is required. The challenges include an appreciation of biological variability, logistical issues pertaining to the proper management of information, the need for robust methods and adequate sample quality with well-designed workflows. At the same time, the economics of pharmacogenetic testing from the perspective of clinicians, patients, governments, insurance companies and pharmaceutical companies will play an important role in determining its future use. Ethical considerations such as informed consent and patient privacy, as well as the role of regulatory bodies in addressing these issues, must be fully understood. Only once these issues are properly dealt with can the full benefits of pharmacogenetics begin to be realised.

摘要

近年来,在药物遗传学领域已经有了一些成功的案例,包括对曲妥珠单抗治疗乳腺癌的 HER2 扩增的分析,以及对血栓形成的华法林剂量的 VKORC1 基因分型。这些研究的令人鼓舞的结果表明,遗传因素确实可能是至少一些药物反应和毒性的重要决定因素。然而,要恰当地应用药物遗传学,需要充分了解该领域的范围和局限性。挑战包括对生物变异性的认识、与正确管理信息相关的后勤问题、对稳健方法的需求以及具有良好设计的工作流程的充足样本质量。与此同时,从临床医生、患者、政府、保险公司和制药公司的角度来看,药物遗传学检测的经济学在决定其未来用途方面将发挥重要作用。必须充分理解知情同意和患者隐私等伦理问题,以及监管机构在解决这些问题方面的作用。只有妥善处理这些问题,才能充分实现药物遗传学的全部益处。

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