Nonparametric and Semiparametric Group Sequential Methods for Comparing Accuracy of Diagnostic Tests

DOI10.1111/J.1541-0420.2008.01000.XMaRDI QIDQ3549406zbMATH OpenOpenAlexWikidataFDO

Authors Liansheng Larry Tang, Scott S. Emerson, Xiao-Hua Zhou

Publication date 22 December 2008

Published in Biometrics (Search for Journal in Brave)

Full work available at URL https://biostats.bepress.com/cgi/viewcontent.cgi?article=1153&context=uwbiostat

zbMATH Keywords

diagnostic accuracyproportional hazard modelweighted AUC

Mathematics Subject Classification ID

Nonparametric hypothesis testing (62G10) Sequential statistical design (62L05) Sequential statistical analysis (62L10) Applications of statistics to biology and medical sciences; meta analysis (62P10)

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Cites work

• A family of nonparametric statistics for comparing diagnostic markers with paired or unpaired data
• Bivariate Exponential Distributions
• Discrete Sequential Boundaries for Clinical Trials
• scientific article; zbMATH DE number 1348603 (Why is no real title available?)
• Semiparametric Receiver Operating Characteristic Analysis to Evaluate Biomarkers for Disease
• Weak convergence and empirical processes. With applications to statistics

Cited in

(12)

• Sample size recalculation in sequential diagnostic trials
• Asymptotic properties of the sequential empirical ROC, PPV and NPV curves under case-control sampling
• scientific article; zbMATH DE number 854950 (Why is no real title available?)
• Assessing the diagnostic accuracy of a sequence of tests
• A framework for covariate-specific ROC curve estimation, with application to biometric recognition
• Group sequential comparison of positive predictive value curves for correlated biomarker data
• Adaptive trial designs in diagnostic accuracy research
• Order-Constrained ROC Regression With Application to Facial Recognition
• Efficient statistical tests to compare Youden index: accounting for contingency correlation
• Repeated significance tests of linear combinations of sensitivity and specificity of a diagnostic biomarker
• Group sequential testing of the predictive accuracy of a continuous biomarker with unknown prevalence
• Early termination of a two-stage study to develop and validate a panel of biomarkers

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