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精准医学与分子癌症研究中的全球不平等现象。

Global Inequities in Precision Medicine and Molecular Cancer Research.

作者信息

Drake Thomas M, Knight Stephen R, Harrison Ewen M, Søreide Kjetil

机构信息

Department of Clinical Surgery, University of Edinburgh, Edinburgh, United Kingdom.

Department of Gastrointestinal Surgery, Stavanger University Hospital, Stavanger, Norway.

出版信息

Front Oncol. 2018 Sep 4;8:346. doi: 10.3389/fonc.2018.00346. eCollection 2018.

Abstract

Precision medicine based upon molecular testing is heralded as a revolution in how cancer is prevented, diagnosed, and treated. Large efforts across the world aim to conduct comprehensive molecular profiling of disease to inform preclinical models, translational research studies and clinical trials. However, most studies have only been performed in patients from high-income countries. As the burden on non-communicable diseases increases, cancer will become a pressing burden across the world, disproportionately affecting low-middle income settings. There is emerging evidence that the molecular landscape of disease differs geographically and by genetic ancestry, which cannot be explained by environmental factors alone. There is a lack of good quality evidence that characterises the molecular landscape of cancers found in low-middle income countries. As cancer medicine becomes increasingly driven by molecular alterations in high-income settings, low-income settings may become left behind. Further efforts on an international scale must be made by researchers, funders, and policymakers to ensure cancer research addresses disease across the world, so models are not limited to subtypes of disease found in high-income countries. In this review, we discuss differences found in the molecular profiles of tumours worldwide and the implication this has for the future of global cancer care. Finally, we identify several barriers currently limiting progress in this field and innovative solutions, which may address these shortcomings.

摘要

基于分子检测的精准医学被誉为癌症预防、诊断和治疗方式的一场革命。世界各地都在大力开展疾病的全面分子谱分析,以为临床前模型、转化研究和临床试验提供信息。然而,大多数研究仅在高收入国家的患者中进行。随着非传染性疾病负担的增加,癌症将成为全球的一项紧迫负担,对中低收入地区的影响尤为严重。越来越多的证据表明,疾病的分子格局因地理位置和遗传血统而异,这无法仅用环境因素来解释。缺乏高质量的证据来描述中低收入国家癌症的分子格局。随着癌症医学在高收入地区越来越受分子改变的驱动,低收入地区可能会被甩在后面。研究人员、资助者和政策制定者必须在国际范围内做出进一步努力,以确保癌症研究涵盖全球各地的疾病,这样模型就不会局限于高收入国家发现的疾病亚型。在这篇综述中,我们讨论了全球肿瘤分子谱中发现的差异及其对全球癌症护理未来的影响。最后,我们确定了目前限制该领域进展的几个障碍以及可能解决这些不足的创新解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8326/6131579/022d2f69a646/fonc-08-00346-g0001.jpg

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