Integrating cancer genomic data into electronic health records.

Integrating cancer genomic data into electronic health records.
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DOI:
10.1186/s13073-016-0371-3
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发表时间:
2016-10-26
期刊:
影响因子:
12.3
通讯作者:
Levy MA
Levy MA
中科院分区:
生物学1区
文献类型:
--
作者:
Warner JL;Jain SK;Levy MA

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基因组靶向治疗和免疫治疗的兴起在过去10-15年中彻底改变了肿瘤学的实践。与此同时,新技术,特别是电子健康记录(EHR)已经渗透到肿瘤诊所。EHR系统最初被设计为计费和临床文档系统,没有预料到需要每天进行审查、解释和采取行动的基因组信息的复杂性和多样性。改进癌症基因组数据与EHR系统的集成将有助于指导临床医生决策,支持二次使用,并最终改善肿瘤诊所内的患者护理。与将癌症基因组数据整合到EHR中的挑战相关的一些关键因素包括:将原始基因组数据转化为有意义的、可操作的结果的生物信息学管道;人类策展在解释变异呼叫中的作用;以及对基因组和临床数据的一致标准的需求。几个新兴的集成模式进行了讨论,在这篇评论中,包括:非标准化的努力,个别机构和基因组检测实验室之间的“中间件”产品,描绘基因组信息,虽然在临床工作流程之外,和应用程序编程接口,有可能在临床工作流程。还讨论了临床基因组知识库的关键需求,这些知识库可以是独立的或集成到上述解决方案中。本文的在线版本(doi:10.1186/s13073-016-0371-3)包含补充材料,可供授权用户使用。
The rise of genomically targeted therapies and immunotherapy has revolutionized the practice of oncology in the last 10–15 years. At the same time, new technologies and the electronic health record (EHR) in particular have permeated the oncology clinic. Initially designed as billing and clinical documentation systems, EHR systems have not anticipated the complexity and variety of genomic information that needs to be reviewed, interpreted, and acted upon on a daily basis. Improved integration of cancer genomic data with EHR systems will help guide clinician decision making, support secondary uses, and ultimately improve patient care within oncology clinics. Some of the key factors relating to the challenge of integrating cancer genomic data into EHRs include: the bioinformatics pipelines that translate raw genomic data into meaningful, actionable results; the role of human curation in the interpretation of variant calls; and the need for consistent standards with regard to genomic and clinical data. Several emerging paradigms for integration are discussed in this review, including: non-standardized efforts between individual institutions and genomic testing laboratories; “middleware” products that portray genomic information, albeit outside of the clinical workflow; and application programming interfaces that have the potential to work within clinical workflow. The critical need for clinical-genomic knowledge bases, which can be independent or integrated into the aforementioned solutions, is also discussed. The online version of this article (doi:10.1186/s13073-016-0371-3) contains supplementary material, which is available to authorized users.
全面的癌症基因面板可用于估计突变负荷,并在临床实践中预测PD-1阻滞的临床益处。
DOI: 10.18632/oncotarget.5950
发表时间: 2015-10-27
期刊: Oncotarget
影响因子: --
作者:
Campesato LF;Barroso-Sousa R;Jimenez L;Correa BR;Sabbaga J;Hoff PM;Reis LF;Galante PA;Camargo AA
通讯作者: Camargo AA
DOI: 10.1038/nature09534
发表时间: 2010-10-28
期刊: NATURE
影响因子: 64.8
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DOI: 10.14694/edbook_am.2014.34.71
发表时间: 2014-01-01
期刊: American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting
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作者:
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影响因子: 6.4
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DOI: 10.1200/jco.2016.68.4316
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期刊: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
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