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Analytical Validation of Protein-Based Multiplex Assays: A Workshop Report by the NCI-FDA Interagency Oncology Task Force on Molecular Diagnostics

机译:基于蛋白质的多重分析的分析验证:NCI-FDA机构间肿瘤学工作组分子诊断研讨会报告

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摘要

Clinical proteomics has the potential to enable the early detection of cancer through the development of multiplex assays that can inform clinical decisions. However, there has been some uncertainty among translational researchers and developers as to the specific analytical measurement criteria needed to validate protein-based multiplex assays. To begin to address the causes of this uncertainty, a day-long workshop titled "Interagency Oncology Task Force Molecular Diagnostics Workshop" was held in which members of the proteomics and regulatory communities discussed many of the analytical evaluation issues that the field should address in development of protein-based multiplex assays for clinical use. This meeting report explores the issues raised at the workshop and details the recommendations that came out of the day's discussions, such as a workshop summary discussing the analytical evaluation issues that specific proteomic technologies should address when seeking US Food and Drug Administration approval. [PUBLICATION ABSTRACT]
机译:临床蛋白质组学具有潜力,可以通过开发可以为临床决策提供依据的多重测定法来早期检测癌症。但是,在转换研究人员和开发人员之间,对于验证基于蛋白质的多重分析所需的特定分析测量标准存在不确定性。为了解决这种不确定性的原因,举行了​​为期一天的研讨会,名为“跨部门肿瘤学工作队分子诊断研讨会”,蛋白质组学和法规界成员讨论了该领域在开发中应解决的许多分析评估问题。基于蛋白质的多重测定用于临床。该会议报告探讨了研讨会上提出的问题,并详细介绍了当天讨论中提出的建议,例如研讨会摘要,讨论了蛋白质组学技术在寻求美国食品和药物管理局批准时应解决的分析评估问题。 [出版物摘要]

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    《Clinical Chemistry》 |2010年第2期|p.237-243|共7页
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    Henry Rodriguez,1* ivana Teak,1 Mehdi Mesri,1 Steven A. Carr,1 Daniel C. Liebler,1 Susan J. Fisher,1 Paul Tempst,1 Tara Hiltke,1 Larry G. Kessler,1 Christopher R. Kinsinger,1 Reena Philip,1 David F. Ransohoff,1 Steven J. Skates,1 Fred E. Regnier,1 N. Leigh Anderson,1 and Elizabeth Mansfield,1 on behalf of the Workshop Participants[dagger]1 National Cancer Institute-Food and Drug Administration Interagency Oncology Task Force on Molecular Diagnostics.* Address correspondence to this author at: Center for Strategic Scientific Initiatives, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892. E-mail: rodriguezh@mail.nih.gov.[dagger] See Appendix for complete list of workshop participants.Received September 17, 2009, accepted November 22, 2009.Previously published online at DOI: 10.1373/clinchem.2009.136416Author Contributions: All authors confirmed they have contributed to the intellectual content of this paper and have met the following 3 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data, (b) drafting or revising the article for intellectual content, and (c) final approval of the published article.Authors' Disclosures of Potential Conflicts of Interest: Upon manuscript submission, all authors completed the Disclosures of Potential Conflict of Interest form. Potential conflicts of interest:Employment or Leadership: P. Tempst, Memorial Sloan-Kettering Cancer Center, F.E. Regnier, Purdue University and Quadraspec.Consultant or Advisory Role: P. Tempst, Yale University Medical School, F.E. Regnier, Quadraspec.Stock Ownership: F.E. Regnier, BG Medicine, Quadraspec, and Predictive Physiology and Medicine.Honoraria: None declared.Research Funding: D.C. Liebler, NCI, P. Tempst, NCI/NIH, F.E. Regnier, NCI.Expert Testimony: F.E. Regnier, Pharmacia versus Genentech.Other Remuneration: S. Skates, Teva Inc. (for travel to a scientific conference in Tel Aviv), F.E. Regnier, Gesellschaft Deutscher Chemiker (GDCh) (for travel to, and other expenses related to attending, HPLC 2009 in Dresden).Role of Sponsor: The funding organizations played a direct role in the review and interpretation of data and the preparation or approval of manuscript.,;

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