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Targeting the Optimal Design in Randomized Clinical Trials with Binary Outcomes and No Covariate: Theoretical Study

Author

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  • Chambaz Antoine

    (Laboratoire MAP5, Université Paris Descartes and CNRS)

  • van der Laan Mark J.

    (University of California, Berkeley)

Abstract

This article is devoted to the asymptotic study of adaptive group sequential designs in the case of randomized clinical trials (RCTs) with binary treatment, binary outcome and no covariate. By adaptive design, we mean in this setting a RCT design that allows the investigator to dynamically modify its course through data-driven adjustment of the randomization probability based on data accrued so far, without negatively impacting on the statistical integrity of the trial. By adaptive group sequential design, we refer to the fact that group sequential testing methods can be equally well applied on top of adaptive designs. We obtain that, theoretically, the adaptive design converges almost surely to the targeted unknown randomization scheme. In the estimation framework, we obtain that our maximum likelihood estimator of the parameter of interest is a strongly consistent estimator, and it satisfies a central limit theorem. We can estimate its asymptotic variance, which is the same as that it would feature had we known in advance the targeted randomization scheme and independently sampled from it. Consequently, inference can be carried out as if we had resorted to independent and identically distributed (iid) sampling. In the testing framework, we obtain that the multidimensional t-statistic that we would use under iid sampling still converges to the same canonical distribution under adaptive sampling. Consequently, the same group sequential testing can be carried out as if we had resorted to iid sampling.

Suggested Citation

  • Chambaz Antoine & van der Laan Mark J., 2011. "Targeting the Optimal Design in Randomized Clinical Trials with Binary Outcomes and No Covariate: Theoretical Study," The International Journal of Biostatistics, De Gruyter, vol. 7(1), pages 1-32, January.
  • Handle: RePEc:bpj:ijbist:v:7:y:2011:i:1:n:10
    DOI: 10.2202/1557-4679.1247
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    References listed on IDEAS

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    1. Hu, Feifang & Rosenberger, William F., 2003. "Optimality, Variability, Power: Evaluating Response-Adaptive Randomization Procedures for Treatment Comparisons," Journal of the American Statistical Association, American Statistical Association, vol. 98, pages 671-678, January.
    2. Tymofyeyev, Yevgen & Rosenberger, William F. & Hu, Feifang, 2007. "Implementing Optimal Allocation in Sequential Binary Response Experiments," Journal of the American Statistical Association, American Statistical Association, vol. 102, pages 224-234, March.
    3. William F. Rosenberger & Nigel Stallard & Anastasia Ivanova & Cherice N. Harper & Michelle L. Ricks, 2001. "Optimal Adaptive Designs for Binary Response Trials," Biometrics, The International Biometric Society, vol. 57(3), pages 909-913, September.
    4. Chambaz Antoine & van der Laan Mark J., 2011. "Targeting the Optimal Design in Randomized Clinical Trials with Binary Outcomes and No Covariate: Simulation Study," The International Journal of Biostatistics, De Gruyter, vol. 7(1), pages 1-30, January.
    5. van der Laan Mark J. & Rubin Daniel, 2006. "Targeted Maximum Likelihood Learning," The International Journal of Biostatistics, De Gruyter, vol. 2(1), pages 1-40, December.
    6. Anastasios A. Tsiatis, 2003. "On the inefficiency of the adaptive design for monitoring clinical trials," Biometrika, Biometrika Trust, vol. 90(2), pages 367-378, June.
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    Cited by:

    1. Antoine Chambaz & Mark J. Laan, 2014. "Inference in Targeted Group-Sequential Covariate-Adjusted Randomized Clinical Trials," Scandinavian Journal of Statistics, Danish Society for Theoretical Statistics;Finnish Statistical Society;Norwegian Statistical Association;Swedish Statistical Association, vol. 41(1), pages 104-140, March.
    2. Chambaz Antoine & van der Laan Mark J., 2011. "Targeting the Optimal Design in Randomized Clinical Trials with Binary Outcomes and No Covariate: Simulation Study," The International Journal of Biostatistics, De Gruyter, vol. 7(1), pages 1-30, January.

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