Transcript Slide 1

Bayesian Approach For
Clinical Trials
Mark Chang, Ph.D.
Executive Director
Biostatistics and Data management
AMAG Pharmaceuticals Inc.
[email protected]
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
Current data =>
Weighting
average
Probability of outcome =>
posterior probability
Likelihood function
P(data| H)P(H)
P(H| data) 
P(data)
Effects of Priors on Posterior
– A Simple Example of Weighting Average
Mean difference
Sample
size
Standard
variance
Normal Prior
µ0
(5)
n
(40)
2/n
(0.1)
Trial data
(Frequentist)
Xm
(7)
m
(200)
2/m
(0.02)
(nµ0 + mxm) /(m+n)
m+n
(240)
2/(m+n)
(0.017)
Normal
Posterior
(Bayesian)
(6.67)
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.
Bayesian Approach Basics (1)
Bayesian Approach Basics (2)
Bayesian Approach Basics (3)
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?
Effect size 10%
20%
30%
Power
0.80
0.99
0.29
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
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
1.
2.
3.
4.
5.
6.
7.
8.
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
Bayecian Dose Response Trials
Using ExpDesign Studio 5.0
Bayecian Dose Response Trials
Using ExpDesign Studio (Cont)
Bayecian Dose Response Trials
Using ExpDesign Studio (Cont)
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.
