Pivotal evaluation of the accuracy of a biomarker used for classification or prediction: standards for study design

Research methods for biomarker evaluation lag behind those for evaluating therapeutic treatments. Although a phased approach to development of biomarkers exists and guidelines are available for reporting study results, a coherent and comprehensive set of guidelines for study design has not been deli...

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Vydané v:	JNCI : Journal of the National Cancer Institute Ročník 100; číslo 20; s. 1432
Hlavní autori:	Pepe, Margaret S, Feng, Ziding, Janes, Holly, Bossuyt, Patrick M, Potter, John D
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States 15.10.2008
Predmet:	Biomarkers, Tumor - analysis Case-Control Studies Humans Neoplasms - classification Neoplasms - diagnosis Predictive Value of Tests Research Design
ISSN:	1460-2105, 1460-2105
On-line prístup:	Zistit podrobnosti o prístupe
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Abstract	Research methods for biomarker evaluation lag behind those for evaluating therapeutic treatments. Although a phased approach to development of biomarkers exists and guidelines are available for reporting study results, a coherent and comprehensive set of guidelines for study design has not been delineated. We describe a nested case-control study design that involves prospective collection of specimens before outcome ascertainment from a study cohort that is relevant to the clinical application. The biomarker is assayed in a blinded fashion on specimens from randomly selected case patients and control subjects in the study cohort. We separately describe aspects of the design that relate to the clinical context, biomarker performance criteria, the biomarker test, and study size. The design can be applied to studies of biomarkers intended for use in disease diagnosis, screening, or prognosis. Common biases that pervade the biomarker research literature would be eliminated if these rigorous standards were followed.
AbstractList	Research methods for biomarker evaluation lag behind those for evaluating therapeutic treatments. Although a phased approach to development of biomarkers exists and guidelines are available for reporting study results, a coherent and comprehensive set of guidelines for study design has not been delineated. We describe a nested case-control study design that involves prospective collection of specimens before outcome ascertainment from a study cohort that is relevant to the clinical application. The biomarker is assayed in a blinded fashion on specimens from randomly selected case patients and control subjects in the study cohort. We separately describe aspects of the design that relate to the clinical context, biomarker performance criteria, the biomarker test, and study size. The design can be applied to studies of biomarkers intended for use in disease diagnosis, screening, or prognosis. Common biases that pervade the biomarker research literature would be eliminated if these rigorous standards were followed. Research methods for biomarker evaluation lag behind those for evaluating therapeutic treatments. Although a phased approach to development of biomarkers exists and guidelines are available for reporting study results, a coherent and comprehensive set of guidelines for study design has not been delineated. We describe a nested case-control study design that involves prospective collection of specimens before outcome ascertainment from a study cohort that is relevant to the clinical application. The biomarker is assayed in a blinded fashion on specimens from randomly selected case patients and control subjects in the study cohort. We separately describe aspects of the design that relate to the clinical context, biomarker performance criteria, the biomarker test, and study size. The design can be applied to studies of biomarkers intended for use in disease diagnosis, screening, or prognosis. Common biases that pervade the biomarker research literature would be eliminated if these rigorous standards were followed.Research methods for biomarker evaluation lag behind those for evaluating therapeutic treatments. Although a phased approach to development of biomarkers exists and guidelines are available for reporting study results, a coherent and comprehensive set of guidelines for study design has not been delineated. We describe a nested case-control study design that involves prospective collection of specimens before outcome ascertainment from a study cohort that is relevant to the clinical application. The biomarker is assayed in a blinded fashion on specimens from randomly selected case patients and control subjects in the study cohort. We separately describe aspects of the design that relate to the clinical context, biomarker performance criteria, the biomarker test, and study size. The design can be applied to studies of biomarkers intended for use in disease diagnosis, screening, or prognosis. Common biases that pervade the biomarker research literature would be eliminated if these rigorous standards were followed.
Author	Bossuyt, Patrick M Feng, Ziding Pepe, Margaret S Janes, Holly Potter, John D
Author_xml	– sequence: 1 givenname: Margaret S surname: Pepe fullname: Pepe, Margaret S email: mspepe@u.washington.edu organization: Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA. mspepe@u.washington.edu – sequence: 2 givenname: Ziding surname: Feng fullname: Feng, Ziding – sequence: 3 givenname: Holly surname: Janes fullname: Janes, Holly – sequence: 4 givenname: Patrick M surname: Bossuyt fullname: Bossuyt, Patrick M – sequence: 5 givenname: John D surname: Potter fullname: Potter, John D
BackLink	https://www.ncbi.nlm.nih.gov/pubmed/18840817$$D View this record in MEDLINE/PubMed
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SubjectTerms	Biomarkers, Tumor - analysis Case-Control Studies Humans Neoplasms - classification Neoplasms - diagnosis Predictive Value of Tests Research Design
Title	Pivotal evaluation of the accuracy of a biomarker used for classification or prediction: standards for study design
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