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Accepting risk in the acceleration of drug development for rare cancers

机译:接受罕见癌症加速药物开发的风险

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Rare cancers collectively contribute a disproportionate fraction of the total burden of cancer. The oncology community is increasingly facing small numbers of patients with each cancer subtype, requiring cooperation and collaboration to complete multicentre trials that advance knowledge and patient care. At the same time, new insights into the biology of rare cancers have led to an explosion in knowledge and development of targeted agents. These insights and techniques are set to revolutionise the care of patients with cancer. However, drug development strategies and the availability of new agents for rare cancers are at risk of stalling owing to the ever-increasing complexity and costs of clinical trials. Finding solutions to these problems is imperative to the future of cancer care. We propose that a greater degree of risk sharing is needed than is currently accepted to enable the use of new methods with confidence, and to keep pace with scientific advancement.
机译:罕见的癌症共同构成了癌症总负担的不成比例的部分。肿瘤学界正越来越多地面对每种癌症亚型的少数患者,需要合作与协作才能完成多中心试验,以提高知识和患者护理水平。同时,对稀有癌症生物学的新见解导致靶向药物的知识和开发激增。这些见解和技术将彻底改变癌症患者的护理。然而,由于不断增加的复杂性和临床试验费用,药物开发策略和罕见癌症新药的上市面临停滞的风险。寻找这些问题的解决方案对癌症治疗的未来至关重要。我们建议需要比当前公认的方式更大程度的风险分担,以便能够自信地使用新方法并与科学进步保持同步。

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