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J Kyle Wathen

Publications and source records attributed to J Kyle Wathen.

3 recordsLinked to original sources

Continuous Bayesian adaptive randomization based on event times with covariates.

In comparative clinical trials, the randomization probabilities may be unbalanced adaptively by utilizing the interim data available at each patient's entry time to favour the treatment or treatments having comparatively superior outcomes. This is ethically appealing because, on average, more patients are assigned to the more successful treatments. Consequently, physicians are more likely to enroll patients onto trials where the randomization is outcome-adaptive rather than balanced in the conventional manner. Outcome-adaptive methods based on a binary variable may be applied by reducing an event time to the indicator of the event's occurrence within a predetermined time interval. This results in a loss of information, however, since it ignores the censoring times of patients who have not experienced the event but whose evaluation interval is not complete. This paper proposes and compares exact and approximate Bayesian outcome-adaptive randomization procedures based on time-to-event outcomes. The procedures account for baseline prognostic covariates, and they may be applied continuously over the course of the trial. We illustrate these methods by application to a phase II selection trial in acute leukaemia. A simulation study in the context of this trial is presented.

Antineoplastic Agents↗

Covariate-adjusted adaptive randomization in a sarcoma trial with multi-stage treatments.

We present a Bayesian design for a multi-centre, randomized clinical trial of two chemotherapy regimens for advanced or metastatic unresectable soft tissue sarcoma. After randomization, each patient receives up to four stages of chemotherapy, with the patient's disease evaluated after each stage and categorized on a trinary scale of severity. Therapy is continued to the next stage if the patient's disease is stable, and is discontinued if either tumour response or treatment failure is observed. We assume a probability model that accounts for baseline covariates and the multi-stage treatment and disease evaluation structure. The design uses covariate-adjusted adaptive randomization based on a score that combines the patient's probabilities of overall treatment success or failure. The adaptive randomization procedure generalizes the method proposed by Thompson (1933) for two binomial distributions with beta priors. A simulation study of the design in the context of the sarcoma trial is presented.

Antineoplastic Agents↗

Hierarchical Bayesian approaches to phase II trials in diseases with multiple subtypes.

We propose a methodology for conducting phase II clinical trials in settings where the disease is categorized into multiple subtypes. A hierarchical Bayesian model is assumed for treatment effects within the subtypes. The hierarchical model, which is tailored to each particular application, allows treatment effects to differ across subtypes while assuming a priori that the effects are exchangeable and correlated. Two applications are described. The first is a trial of imatinib for sarcoma in which treatment activity is characterized by a binary indicator of tumour response. The second is a phase II trial of a new preparative regimen for allogeneic bone marrow transplantation in patients with haematologic malignancies, with treatment effect characterized by the mean time from transplant to disease progression or death. The applications illustrate how the hierarchical Bayesian model borrows strength across subtypes.

Antineoplastic Agents↗