Title of article :
Optimal designs for contingent response models with application to toxicity–efficacy studies
Author/Authors :
Rabie، نويسنده , , Huwaida and Flournoy، نويسنده , , Nancy، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
9
From page :
1371
To page :
1379
Abstract :
We describe a general family of contingent response models. These models have ternary outcomes constructed from two Bernoulli outcomes, where one outcome is only observed if the other outcome is positive. This family is represented in a canonical form which yields general results for its Fisher information. A bivariate extreme value distribution illustrates the model and optimal design results. To provide a motivating context, we call the two binary events that compose the contingent responses toxicity and efficacy. Efficacy or lack thereof is assumed only to be observable in the absence of toxicity, resulting in the ternary response (toxicity, efficacy without toxicity, neither efficacy nor toxicity). The rate of toxicity, and the rate of efficacy conditional on no toxicity, are assumed to increase with dose. While optimal designs for contingent response models are numerically found, limiting optimal designs can be expressed in closed forms. In particular, in the family of four parameter bivariate location-scale models we study, as the marginal probability functions of toxicity and no efficacy diverge, limiting D optimal designs are shown to consist of a mixture of the D optimal designs for each failure (toxicity and no efficacy) univariately. Limiting designs are also obtained for the case of equal scale parameters.
Keywords :
Experimental design , Continuation ratio model , Phase II clinical trials , Bivariate responses , dose-finding , Nonlinear response functions
Journal title :
Journal of Statistical Planning and Inference
Serial Year :
2013
Journal title :
Journal of Statistical Planning and Inference
Record number :
2222375
Link To Document :
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