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dc.contributor.authorRabie, Huwaida
dc.contributor.authorFlournoy, Nancy
dc.date.accessioned2018-09-22T06:32:59Z
dc.date.available2018-09-22T06:32:59Z
dc.date.issued2011-12
dc.identifier.urihttp://dspace.bethlehem.edu:8080/xmlui/handle/123456789/74
dc.description.abstractWe generalize results in the literature to obtain a general family contingent response models. These models have ternary outcomes constructed from two Bernouli 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. D and c optimal designs found numerically for a contingent response model with expected response probabilities taken from a bivariate extreme value distribution illustrate the model and motivate limiting results. Optimal designs for even modestly complex nonlinear response models cannot be expressed in closed form; and this includes the contingent response model. Limiting D optimal designs obtained in closed form can be used to approximate exact D and c optimal designs, as they are shown to be efficient over a wide range of parameter values, or they can be used to provide starting values in numerical searches for exact optimal designs. To provide a motivating context, we describe the two binary outcomes that compose the contingent responses as toxicity and no 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. The results provided in this paper are useful for the construction of efficient designs under a broad class of such modelsen_US
dc.language.isoenen_US
dc.publisherIssac Newton Institute for Mathematical Sciencesen_US
dc.subjectDose-finding, experimental design, continuation ratio model, nonlinear response functions, phase II clinical trials, bivariate responsesen_US
dc.titleOptimal designs for contingent response models with application to toxicity and efficacyen_US
dc.typeTechnical Reporten_US


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