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Bayesian Approach For Clinical Trials Mark Chang, Ph.D. Executive Director Biostatistics and Data management AMAG Pharmaceuticals Inc. Mark.Chang@Statisticians.org MBC August 28, 2008, Boston, USA. Outlines. Basics of Bayesian Approach Frequentist Power versus Bayesian Power
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Bayesian Approach For Clinical Trials Mark Chang, Ph.D. Executive Director Biostatistics and Data management AMAG Pharmaceuticals Inc. Mark.Chang@Statisticians.org MBC August 28, 2008, Boston, USA
Outlines • Basics of Bayesian Approach • Frequentist Power versus Bayesian Power • Bayesianism for Different Phases of Trials • Bayesian Decision Approach – Classic and Adaptive • Bayesian Trial Simulations • Summary
Frequentist & Bayesian Paradigms • Many believe that the probability concepts from Frequentist and Bayesian are different. However, from decision-making point of view, we do not differentiate them. • Frequentist: type I and type II error for trial design and p-values, point estimate, and confidence intervals for analysis. • Bayesianism: prior distribution about model parameter (e.g., population mean treatment effect), combined with evidence from a clinical trial (likelihood function) to form the posterior distribution - the updated knowledge about the parameter.
Frequentist Fixed versus Bayesian Distributional Parameters • Our action taken is not upon the truth because the truth is always a mystery. We make decision is upon what we know about the truth, or more precisely based on what we think the truth is. • Semantic: Parameter => Fixed & Unknown • Knowledge about => distribution
Illustration of Bayesian Approach Prior knowledge => Prior probability Weighting average Probability of outcome => posterior probability Current data => Likelihood function
Effects of Priors on Posterior – A Simple Example of Weighting Average
The Key Components for A Bayesian Approach • Parametric Statistical Model • Modeling the underline mechanics • Prior distribution • Probability distribution of model parameters using evidences before the experiment. • Likelihood function • Probability distribution of model parameters using evidences from the experiment. • Posterior distribution • Probability distribution of model parameters derived from the products of prior and likelihood function. • Predictive probability • Probability distribution of future patient’s outcomes based on posterior distribution. • Utility function • A single index measuring overall gains of the treatment, which could include efficacy, safety and etc.
Power with Uncertainty of Treatment Effect (Prior) • Treatment difference is a fixed but unknown value • Prior response rate = 10%, 20%, or 30% with 1/3 probability each. • Power = 80% based on n = 784, average effect size =20%, or • Power = (0.29+0.80+0.99)/3 = 0.69?
Power, Power? Power! • Probability of showing p-value < alpha • Conditional or unconditional probability? • Only 5% Phase I trials are eventually get approved. • About 40% Phase III trials get approved, but 80%-95% power when the trials are designed.
Some Common Misconcepts • Alpha = 2.5% => control false positive drug in the market no more than 2.5%. • If all test drugs in phase-III are effective, then type-I error rate = 0%. If all test drugs in phase-III are ineffective, then type-I error rate = 100% • Confidence interval = Bayesian Credible Interval • Coverage probability concerns a set of CIs with various lengths and locations. • Maturity of data is a requirement of rejecting the null hypothesis of no treatment difference
When Should Bayesian Approach be used • Phase – I • Safety response models with various doses or regiments • Phase –II • Efficacy and safety response models; Dose selection • Phase – III • Determine sample size based on utility • Phase IV • Better and more informative trial design
Bayesian Approach for Multiple-Endpoint Problems • All stepwise or sequential procedures in Frequentist use a sort of “composite endpoint”: Rejection Criterion for the k-th null hypothesis: pk< F(alpha, p1, p2,…,pk-1) Q(p1, p2,…,pk) < alpha
Bayesian Decision Approach for Pivotal Trials (cont.) Time and Financial Constraints: Nmax.
Bayesian Adaptive Design • Adaptive versus static • Conditional versus unconditional • Decision difference under repeated experiments vs. one time event in life • Expected utility of life insurance is negative, we buy it because we have one life and a death will great impact on family member. • Flip a coin, if head, gain $1.5m; if tail, lose $1m. Do you play? (Think about playing one time versus many times)
Basic Steps for A Bayesian Trial Design • Identify trial objectives • Select statistical model . • Determine the priors for the model parameters. • Calculate likelihood function (joint probability) based on simulated data. • Calculate the posterior probability. • Define utility function. • Specify constraints • Perform optimization to maximize the utility
Advanced Techniques • Hierarchical model • Non-conjugate distributions and MCMC
Summary • Drug development involves a sequence of decision process where Bayesian adaptive approach provides powerful solutions that traditional frequentist can not provide. • Computer simulations for Bayesian adaptive design could provide predictions on trial outcomes under various scenarios and therefore allows us to select optimal design • It is likely that a hybrid Frequenstist-Bayesian approach would be used before adoption of full Bayesian in larger scale for clinical trials.
References • Mark Chang, Classical and Adaptive Clinical Trial Designs Using ExpDesign Studio (Includes ExpDesign 5.0 software CD). John-Wiley, 2008. • Mark Chang, Adaptive Design Theory and Implementations Using SAS and R, Chapman & Hall/CRC, 2007.