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Bayesian pairwise meta-analysis of time-to-event outcomes in the presence of non-proportional hazards: A simulation study of flexible parametric, piecewise exponential and fractional polynomial models

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Version 2 2024-10-18, 10:49
Version 1 2024-05-21, 08:55
journal contribution
posted on 2024-10-18, 10:49 authored by Suzanne Freeman, Alex Sutton, Nicola Cooper, Alessandro Gasparini, Michael Crowther, Neil Hawkins

Background: Traditionally, meta-analysis of time-to-event outcomes reports a single pooled hazard ratio assuming proportional hazards (PH). For health technology assessment evaluations, hazard ratios are frequently extrapolated across a lifetime horizon. However, when treatment effects vary over time, an assumption of PH is not always valid. The Royston-Parmar (RP), piecewise exponential (PE), and fractional polynomial (FP) models can accommodate non-PH and provide plausible extrapolations of survival curves beyond observed data.


Methods: Simulation study to assess and compare the performance of RP, PE, and FP models in a Bayesian framework estimating restricted mean survival time difference (RMSTD) at 50 years from a pairwise meta-analysis with evidence of non-PH. Individual patient data were generated from a mixture Weibull distribution. Twelve scenarios were considered varying the amount of follow-up data, number of trials in a meta-analysis, non-PH interaction coefficient, and prior distributions. Performance was assessed through bias and mean squared error. Models were applied to a metastatic breast cancer example.


Results: FP models performed best when the non-PH interaction coefficient was 0.2. RP models performed best in scenarios with complete follow-up data. PE models performed well on average across all scenarios. In the metastatic breast cancer example, RMSTD at 50-years ranged from -14.6 to 8.48 months.


Conclusions: Synthesis of time-to-event outcomes and estimation of RMSTD in the presence of non-PH can be challenging and computationally intensive. Different approaches make different assumptions regarding extrapolation and sensitivity analyses varying key assumptions are essential to check the robustness of conclusions to different assumptions for the underlying survival function.

Funding

This is a summary of independent research funded by a National Institute for Health Research(NIHR) Post-Doctoral Fellowship (PDF-2018-11-ST2-007) and carried out at the National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC) and Applied Research Collaboration East Midlands (ARC EM).

History

Author affiliation

College of Life Sciences Population Health Sciences

Version

  • VoR (Version of Record)

Published in

Research Synthesis Methods

Volume

15

Issue

5

Pagination

701-824

Publisher

Wiley

issn

1759-2879

eissn

1759-2887

Copyright date

2024

Available date

2024-10-18

Language

en

Deposited by

Dr Suzanne Freeman

Deposit date

2024-05-20

Data Access Statement

The data generated for the simulation study and all R and OpenBUGS code for the simulationstudy are available on GitHub: https://github.com/SCFreeman/Simulation1. The full IPD for the metastatic breast cancer example is available on GitHub: https://github.com/SCFreeman/Simulation1.

Rights Retention Statement

  • No

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