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Translating cancer research into targeted therapeutics

机译:将癌症研究转化为靶向疗法

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摘要

The emphasis in cancer drug development has shifted from cytotoxic, non-specific chemotherapies to molecularly targeted, rationally designed drugs promising greater efficacy and less side effects. Nevertheless, despite some successes drug development remains painfully slow. Here, we highlight the issues involved and suggest ways in which this process can be improved and expedited. We envision an increasing shift to integrated cancer research and biomarker-driven adaptive and hypothesis testing clinical trials. The goal is the development of specific cancer medicines to treat the individual patient, with treatment selection being driven by a detailed understanding of the genetics and biology of the patient and their cancer.
机译:癌症药物开发的重点已从细胞毒性非特异性化学疗法转移到分子靶向,合理设计的药物,这些药物有望带来更高的疗效和更少的副作用。然而,尽管取得了一些成功,药物开发仍然非常缓慢。在这里,我们重点介绍了所涉及的问题,并提出了可以改进和加快该过程的方法。我们设想将越来越多地转向综合癌症研究以及生物标记物驱动的适应性和假设测试临床试验。目标是开发治疗个体患者的特定癌症药物,治疗选择的选择取决于对患者及其癌症的遗传和生物学的详细了解。

著录项

  • 来源
    《Nature》 |2010年第7315期|P.543-549iii|共8页
  • 作者

    J. S. de Bono; Alan Ashworth;

  • 作者单位

    The Institute of Cancer Research, Cotswold Road, Sutton, Surrey SM2 5NG, UK The Royal Marsden NHS Foundation Trust, Downs Road, Sutton, Surrey, SM2 5PT, UK;

    rnThe Breakthrough Breast Cancer Centre, The Institute of Cancer Research, Fulham Road, London SW3 6JB, UK;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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