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Theory and Methods

Adaptive Multivariate Global Testing

Pages 613-623 | Received 01 Apr 2013, Published online: 13 Jun 2014

REFERENCES

  • Bauer, P., Köhne, K. (1994), Evaluation of Experiments With Adaptive Interim Analyses, Biometrics, 50, 1029–1041.
  • Brannath, W., Gutjahr, G., Bauer, P. (2012), Probabilistic Foundation of Confirmatory Adaptive Designs, Journal of the American Statistical Association, 107, 824–832.
  • Brannath, W., Posch, M., Bauer, P. (2002), Recursive Combination Tests, Journal of the American Statistical Association, 97, 236–244.
  • Bretz, F., Koenig, F., Brannath, W., Glimm, E., Posch, M. (2009), Adaptive Designs for Confirmatory Clinical Trials, Statistics in Medicine, 28, 1181–1217.
  • D’Agostino, R. B., and Russell, H. K. (2005), Multiple Endpoints, Multivariate Global Tests, New York: Wiley.
  • Davidson, R.J., Pizzagalli, D., Nitschke, J.B., Putnam, K. (2002), Depression: Perspectives From Affective Neuroscience, Annual Review of Psychology, 53, 545–574.
  • Denne, J.S., Jennison, C. (2000), A Group Sequential T-test With Updating of Sample Size, Biometrika, 87, 125–134.
  • Follmann, D. (1996), A Simple Multivariate Test for One-Sided Alternatives, Journal of the American Statistical Association, 91, 854–861.
  • Gelman, A., Carlin, J. B., Stern, H. S., and Rubin, D. B. (2004), Bayesian Data Analysis, Boca Raton, FL: Chapman & Hall.
  • Hotelling, H. (1931), The Generalization of Student’s Ratio, The Annals of Mathematical Statistics, 2, 360–378.
  • Kieser, M., Schneider, B., Friede, T. (2002), A Bootstrap Procedure for Adaptive Selection of the Test Statistic in Flexible Two-Stage Designs, Biometrical Journal, 44, 641–652.
  • Kimani, P.K., Stallard, N., Hutton, J.L. (2009), Dose Selection in Seamless Phase II/III Clinical Trials Based on Efficacy and Safety, Statistics in Medicine, 28, 917–936.
  • Lang, T., Auterith, A., Bauer, P. (2000), Trendtests With Adaptive Scoring, Biometrical Journal, 42, 1007–1020.
  • Läuter, J., Glimm, E., Kropf, S. (1996), New Multivariate Tests for Data With an Inherent Structure, Biometrical Journal, 38, 1–23.
  • Läuter, J., Glimm, E., Kropf, S. (1998), “Multivariate Tests Based on Left-Spherically Distributed Linear Scores, The Annals of Statistics, 26, 1972–1988.
  • Lehmacher, W., Wassmer, G. (1999), Adaptive Sample Size Calculations in Group Sequential Trials, Biometrics, 55, 1286–1290.
  • Liu, Q., Proschan, M.A., Pledger, G.W. (2002), A Unified Theory of Two-Stage Adaptive Designs, Journal of the American Statistical Association, 97, 1034–1041.
  • Logan, B.R., Tamhane, A.C. (2004), On O’Brien’s OLS and GLS Tests for Multiple Endpoints, Lecture Notes-Monograph Series, 47, 76–88.
  • Mehta, C.R., Pocock, S.J. (2011), Adaptive Increase in Sample Size When Interim Results are Promising: A Practical Guide With Examples, Statistics in Medicine, 30, 3267–3284.
  • Minas, G., Rigat, F., Nichols, T.E., Aston, J.A. D., Stallard, N. (2012), A Hybrid Procedure for Detecting Global Treatment Effects in Multivariate Clinical Trials: Theory and Applications to fMRI Studies, Statistics in Medicine, 31, 253–268.
  • Müller, H.-H., Schäfer, H. (2001), Adaptive Group Sequential Designs for Clinical Trials: Combining the Advantages of Adaptive and of Classical Group Sequential Approaches, Biometrics, 57, 886–891.
  • O’Brien, P.C. (1984), Procedures for Comparing Samples With Multiple Endpoints, Biometrics, 40, 1079–1087.
  • O’Hagan, A., Stevens, J. W. (2001), Bayesian Assessment of Sample Size for Clinical Trials of Cost-Effectiveness, Medical Decision Making, 21, 219–230.
  • Pocock, S.J., Geller, N.L., Tsiatis, A.A. (1987), The Analysis of Multiple End-Points in Clinical-Trials, Biometrics, 43, 487–498.
  • Proschan, M.A., Hunsberger, S.A. (1995), Designed Extension of Studies Based on Conditional Power, Biometrics, 51, 1315–1324.
  • Spiegelhalter, D., Abrams, K. R., and Myles, J. (2002), Bayesian Approaches to Clinical Trials and Health-Care Evaluation, Chichester: Wiley.
  • Tang, D.-I., Geller, N.L., Pocock, S.J. (1993), On the Design and Analysis of Randomized Clinical Trials With Multiple Endpoints, Biometrics, 49, 23–30.
  • Tang, D.-I., Gnecco, C., Geller, N.L. (1989a), An Approximate Likelihood Ratio Test for a Normal Mean Vector With Nonnegative Components With Application to Clinical Trials, Biometrika, 76, 577–583.
  • Tang, D.-I., Gnecco, C., Geller, N.L. (1989b), Design of Group Sequential Clinical Trials With Multiple Endpoints, Journal of the American Statistical Association, 84, 776–779.
  • Westfall, P.H., Krishen, A., Young, S.S. (1998), Using Prior Information to Allocate Significance Levels for Multiple Endpoints, Statistics in Medicine, 17, 2107–2119.
  • Zhu, H.J., Hu, F.F. (2010), Sequential Monitoring of Response-Adaptive Randomized Clinical Trials, The Annals of Statistics, 38, 2218–2241.