1 / 26

Treatment Switching in the VenUS IV trial

Treatment Switching in the VenUS IV trial. Methods to manage treatment non-compliance in RCTs with time-to-event outcomes. Caroline Fairhurst York Trials Unit. Context. Two arm RCT Clinical setting Continuous treatment Time-to-event outcome (e.g., death, healing). Dream or reality?.

clyde
Download Presentation

Treatment Switching in the VenUS IV trial

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Treatment Switching in the VenUS IV trial Methods to manage treatment non-compliance in RCTs with time-to-event outcomes Caroline Fairhurst York Trials Unit

  2. Context • Two arm RCT • Clinical setting • Continuous treatment • Time-to-event outcome (e.g., death, healing)

  3. Dream or reality? Reality • Participants withdraw from the trial and are lost to follow-up • Withdraw from treatment • Deviate from their allocated trial treatment Ideal • All participants will remain in the trial throughout follow-up • Will be concordant with their allocated treatment • Will provide outcome data

  4. Treatment switching

  5. Problem? • Switching to the alternative trial treatment makes randomised groups more similar • Dilutes the treatment effect observed from a comparison of treatment groups as randomised ignoring deviations from allocated treatment (ITT) • If you want to estimate the effect had fewer switches occurred, ITT analysis biased towards the null of no difference

  6. VenUS IV trial Venous leg ulcers are wounds that form on gaiter region of the leg They are painful, malodorous and prone to infection Difficult to heal and 12 month recurrence rates are 18-28% VenUS I, II, III Four layer bandaging is current gold standard

  7. VenUS IV trial • Population: Patients aged over 18 with at least one venous leg ulcer and able to tolerate high compression to the leg • Intervention: Two layer high compression hosiery • Control: Four layer high compression bandaging • Outcome: Time to healing of the largest ulcer

  8. Treatment switching Randomised n=457 Bandage n=224 Hosiery n=230 Non-trial treatment n=46 Non-trial treatment n=42 n=16 n=46 Bandage Hosiery

  9. Treatment switching Compression uncomfortable Increase in ulcer area Ulcer deterioration

  10. Simple methods - ITT Intention-to-treat • ITT recommended (ICH E9) • Compares individuals in the treatment groups to which they were randomised • Estimates the effect of offering the two treatment policies to patients with whatever subsequent changes may occur • “pragmatic effectiveness not biological efficacy” • But what about effect of receiving experimental treatment?

  11. Simple methods - PP Per-protocol • 1. Excludes patients who switch Assumptions: Switchers have same prognosis as non-switchers so selection bias not introduced • 2. Censor patients at time of switch Assumptions: Decision to switch not related to prognosis so censoring non-informative

  12. Simple methods - TTV Treatment as a time-varying covariate Time-to-event model adjusted for time-dependent treatment covariate: 0, whilst receiving control treatment 1, whilst receiving experimental treatment Breaks randomisation balance and so subject to selection bias if switching related to prognosis trt=

  13. Complex methods Rank Preserving Structural Failure Time Model • Attempt to estimate survival time lost/gained by exposure to experimental treatment • Relate the observed survival time, Ti, to the counterfactual survival time, Uiby Time on control treatment Time on experimental treatment Acceleration factor

  14. RPSFTM • For patients (always) treated with control treatment: Ti1=0 Þ Ti=Ui • For patients (always) treated with experimental treatment Ti0=0 Þ Ti=Ui • Experimental treatment ‘multiplies’ survival time by relative to control treatment

  15. RPSFTM Randomisation Death Control patient Observed Counterfactual Death Treatment patient Observed Counterfactual Expected survival time without active treatment – `shrunk’ by a factor of Control patient who switches Death Observed Counterfactual Time

  16. RPSFTM Grid search for : • Vary values of by a small amount between two plausible minimum and maximum values • Transform observed survival times using • Compare the counterfactual survival times between the two randomised groups (e.g., logrank test or Cox model) • Let be value of which maximises the p-value from the test, then acceleration factor is

  17. Assumptions • Randomisation based treatment effect estimator • Rank preserving: if patient i fails before patient j on treatment A, then i would fail before j on treatment B • Assumes the treatment effect is the same regardless of when patient starts to receive experimental treatment

  18. Complex methods Iterative parameter estimation algorithm • Extension of RPSFTM methods • Assume the same causal model relating actual and counterfactual survival times • Different estimation process for

  19. IPE • A parametric accelerated failure time model is fit to the observed survival times (e.g., Exponential, Weibull) • Initial estimate of acceleration factor is obtained • This is used to create first counterfactual dataset, U1, using

  20. IPE • Same parametric accelerated failure time model is fit to the counterfactual survival time • New estimate of obtained • New counterfactual dataset created Until estimate of converges (is within, say, 10-5 of the previous estimate)

  21. AF or HR? Note • strbee Stata program (Ian White) • ipe option • hr option • Final estimate of , used to ‘correct’ observed survival times • Proportional hazards model used to estimate ‘corrected’ HR

  22. Application to VenUS IV

  23. Simulation • A simulation study suggested that the simple methods can significantly overestimate the true treatment effect, whilst the more complex methods of RPSFTM and IPE produce less biased results

  24. Conclusion • ITT analysis recommended as primary analysis • Consider a method to estimate the true effect of efficacy as secondary analysis, but not PP • Different methods can be used for continuous or categorical variables, e.g. CACE analysis

  25. Acknowledgements • York Trials Unit • VenUS IV trial team • Supervisor, Professor Mike Campbell (ScHARR, Sheffield)

  26. References • Ashby, R. L., et al. (2014). "Clinical and cost-effectiveness of compression hosiery versus compression bandages in treatment of venous leg ulcers (Venous leg Ulcer Study IV, VenUS IV): a randomised controlled trial." The Lancet383(9920): 871-879. • Robins, J. and A. Tsiatis (1991). "Correcting for non-compliance in randomized trials using rank preserving structural failure time models." Communications in Statistics-Theory and Methods20(8): 2609 - 2631. • White, I., et al. (1999). "Randomization-based methods for correcting for treatment changes: Examples from the Concorde trial." Statistics in Medicine18(19): 2617 - 2634. • White, I., et al. (2002). "strbee: Randomization-based efficacy estimator." The Stata Journal2(Number 2): 140 - 150. • Branson, M. and J. Whitehead (2002). "Estimating a treatment effect in survival studies in which patients switch treatment." Statistics in Medicine21: 2449 - 2463.

More Related