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Evidence synthesis of competing interventions when there is inconsistency in how effectiveness outcomes are measured across studies Nicola Cooper Centre for Biostatistics and Genetic Epidemiology, Department of Health Sciences, University of Leicester, UK. http://www.hs.le.ac.uk/group/bge/ Acknowledgements: Tony Ades, Guobing Lu, Alex Sutton & Nicky Welton

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MULTIPLE EVENT OUTCOMES Often the main clinical outcome differs across trials Inconsistent reporting (e.g. mean, median) Change in outcomes used over time Possible to use the available data to inform the estimation of others

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EXAMPLE: Anti-viral for influenza Three antiviral treatments for influenza Amantadine Oseltamivir Zanamivir No direct comparisons of the different antiviral treatments All trials compare antiviral to standard care Different outcome measures Time to alleviation of fever Time to alleviation of ALL symptoms Different summary statistics reported Median time to event Mean time to event

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Oseltamivir and Zanamivir trials report median time to event of interest Amantadine trials report mean time to event of interest No direct comparison trials of all antivirals & standard care. Important to preserve within-trial randomised treatment comparison of each trial whilst combining all available comparisons between treatments (i.e. maintain randomisation). DATA AVAILABLE

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In clinical studies with time to event data as the principal outcome, median time to event usually reported. However, for economic evaluations the statistic of interest is the mean => Area under survival curve (i.e. provides best estimate of expected time to an event ) Often mean time to an event can NOT be determined from observed data alone due to right- censoring (i.e. actual time to an event for some individuals unknown either due to loss of follow-up or event not incurred by end of study) BACKGROUND

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PROBLEM: Mean undefined Last observation censored => mean undefined Trt 1 Trt 2

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CALCULATING MEAN FROM MEDIAN TIME Simplest approach is to assume an Exponential distribution for time with influenza, thus assuming a constant hazard function over time, Probability of still having influenza at time t, At median time, Mean time to event = 1/ & its corresponding variance = 1/ 2 r, where r = number of events incurred during the study period

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THREE STATE MARKOV MODEL 1 = transition rate (hazard) from influenza onset to alleviation of fever 2 = transition rate from alleviation of fever to alleviation of symptoms 1/ 1 = expected time from influenza onset to alleviation of fever 1/ 2 = expected time from alleviation of fever to alleviation of symptoms (1/ 1 + 1/ 2 ) = expected time from influenza onset to alleviation of symptoms 1 2

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Assumptions: Equal treatment effects in each period, jk Baseline hazard during second period same as in first period plus an additional random effect term, j EVIDENCE SYNTHESIS MODEL ln( i1 ) = j + jk = -ln( 1 ) # i1, flu to fev alleviated ln( i2 ) = j + j + jk = -ln( 2 ) # i2, fev to sym alleviated i3 = i1 + i2 = 1/ 1 + 1/ 2 # i3, flu to sym alleviated jk ~ Normal(d k, 2 ) # log hazard ratio j ~ Normal(g, V g ) # random effect where i = trial arms, j = trials, k = treatments. Prior distributions specified for d k, g, 2, V g

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Exp(d k ) is the ratio of hazards of recovery at any time for an individual on treatment k relative to an individual on the standard treatment If exp(d k ) < 1 then treatment k is superior If exp(d k ) > 1 then standard treatment is superior Model fitted in WinBUGS and evaluated using MCMC simulation HAZARD RATIO / RELATIVE HAZARD

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CATERPILLAR PLOT OF HAZARD RATIOS Hazard Ratio Improvement in rate of recovery Oseltamivir Amantadine Zanamivir

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RANKING TREATMENTS Best 0% Best 33% Best 67% Best 1%

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PROPORTION OF INDIVIDUALS IN EACH STATE Influenza All symptoms alleviated Fever alleviated Oseltamivir trials 21 days (8-22%) Zanamivir trials 28 days (7-25%)

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WEIBULL MODEL Relaxes assumption of constant hazard ( = shape) = 1 0 < < 1 = 2 Exponential

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WEIBULL MODEL (cont.) Probability of still having influenza at time t, S(t)=e -(t/ ) >0 (shape) >0 (scale) At median time, 0.5=e -(t med / ) t med = (ln(2)) 1/ If r out of n individuals still had symptoms at X days (i.e. end of trial), the proportion of censored individuals can be expressed as: S(t(X)) =r/n=e -(t/ )

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AVAILABLE TRIAL DATA Trt 1 Trt 2 0.5 t med X r/n

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WEIBULL MODEL (cont.) Important to calculate E(S(t(X))|t med ) to take account of the correlation between median time (t med ) to alleviation of illness and proportion of participants (r/n) still ill at X days as they are from the same trial dataset. Mean time to event (i.e. statistic of interest) (1+1/ )

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EVIDENCE SYNTHESIS MODEL Assumptions: Equal treatment effects in each period, jk Baseline hazard during second period same as in first period plus an additional random effect term, j ln( i1 ) = j + jk = ln( i1 ) + ln( (1+1/ 1 )) # i1, flu to fev alleviated ln( i2 ) = j + j + jk # i2, fev to sym alleviated i3 = i1 + i2 = i3 (1+1/ 3 ) # i3, flu to sym alleviated jk ~ Normal(d k, 2 ) # log hazard ratio j ~ Normal(g, V g ) # random effect where i = trial arms, j = trials, k = treatments. Prior distributions specified for d k, g, 2, V g

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EVIDENCE SYNTHESIS MODEL (cont.) and are the shape and scale parameters of a Weibull distribution respectively Model assumes the shape parameters are the same for time to alleviation of fever, 1, regardless of antiviral treatment & similarly for time to alleviation of symptoms, 3 Due to lack of data, to estimate 1 set equal to 1 (i.e. exponential distribution). Could set constraint to ensure proportion still with fever at X days (i.e. end of trial) proportion still with symptoms

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CATERPILLAR PLOT OF HAZARD RATIOS Improvement in rate of recovery Zanamivir Oseltamivir Amantadine

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RANKING TREATMENTS Best 0% Best 1% Best 20% Best 79%

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CONCLUSIONS Although amantadine is ranked “best” it does have serious side effects (e.g. gastrointestinal symptoms, central nervous system) which are not taken into account in this analysis This type of model could inform the effectiveness parameters of a cost effectiveness decision model Allows multiple outcomes & indirect comparisons to be modelled within a single framework Appropriate model for nested outcomes (e.g. progression- free survival & overall survival) If non-nested outcomes, then a multivariate meta-analysis model, as developed for surrogate outcomes, more appropriate

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