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General Purpose Methods for Simulating Survival Data for Expected Value of Sample Information Calculations

  • Mathyn Vervaart*
  • , Eline Aas
  • , Karl P Claxton
  • , Mark Strong
  • , Nicky J Welton
  • , Torbjørn Wisløff
  • , Anna Heath
  • *Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

5 Citations (Scopus)
1 Downloads (Pure)

Abstract

BACKGROUND: Expected value of sample information (EVSI) quantifies the expected value to a decision maker of reducing uncertainty by collecting additional data. EVSI calculations require simulating plausible data sets, typically achieved by evaluating quantile functions at random uniform numbers using standard inverse transform sampling (ITS). This is straightforward when closed-form expressions for the quantile function are available, such as for standard parametric survival models, but these are often unavailable when assuming treatment effect waning and for flexible survival models. In these circumstances, the standard ITS method could be implemented by numerically evaluating the quantile functions at each iteration in a probabilistic analysis, but this greatly increases the computational burden. Thus, our study aims to develop general purpose methods that standardize and reduce the computational burden of the EVSI data-simulation step for survival data.

METHODS: We developed a discrete sampling method and an interpolated ITS method for simulating survival data from a probabilistic sample of survival probabilities over discrete time units. We compared the general purpose and standard ITS methods using an illustrative partitioned survival model with and without adjustment for treatment effect waning.

RESULTS: The discrete sampling and interpolated ITS methods agree closely with the standard ITS method, with the added benefit of a greatly reduced computational cost in the scenario with adjustment for treatment effect waning.

CONCLUSIONS: We present general purpose methods for simulating survival data from a probabilistic sample of survival probabilities that greatly reduce the computational burden of the EVSI data-simulation step when we assume treatment effect waning or use flexible survival models. The implementation of our data-simulation methods is identical across all possible survival models and can easily be automated from standard probabilistic decision analyses.

HIGHLIGHTS: Expected value of sample information (EVSI) quantifies the expected value to a decision maker of reducing uncertainty through a given data collection exercise, such as a randomized clinical trial. In this article, we address the problem of computing EVSI when we assume treatment effect waning or use flexible survival models, by developing general purpose methods that standardize and reduce the computational burden of the EVSI data-generation step for survival data.We developed 2 methods for simulating survival data from a probabilistic sample of survival probabilities over discrete time units, a discrete sampling method and an interpolated inverse transform sampling method, which can be combined with a recently proposed nonparametric EVSI method to accurately estimate EVSI for collecting survival data.Our general purpose data-simulation methods greatly reduce the computational burden of the EVSI data-simulation step when we assume treatment effect waning or use flexible survival models. The implementation of our data-simulation methods is identical across all possible survival models and can therefore easily be automated from standard probabilistic decision analyses.

Original languageEnglish
Pages (from-to)595-609
Number of pages15
JournalMedical Decision Making
Volume43
Issue number5
Early online date27 Mar 2023
DOIs
Publication statusPublished - 1 Jul 2023

Bibliographical note

Funding Information:
The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: MV, EA, KC, MS, NJW, and TW were funded by a grant from the Norwegian Research Council through NordForsk (grant 298854). AH was supported by a Canada Research Chair in Statistical Trial Design and the Natural Sciences and Engineering Research Council of Canada (grant RGPIN-2021-03366) The funding agreement ensured the authors’ independence in designing the study, interpreting the data, writing, and publishing the report.

Publisher Copyright:
© The Author(s) 2023.

Research Groups and Themes

  • HEHP@Bristol

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