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

Author:

Vervaart Mathyn1ORCID,Aas Eline12,Claxton Karl P.34,Strong Mark5ORCID,Welton Nicky J.6,Wisløff Torbjørn7ORCID,Heath Anna8910ORCID

Affiliation:

1. Department of Health Management and Health Economics, University of Oslo, Oslo, Norway

2. Division of Health Services, Norwegian Institute of Public Health, Oslo, Norway

3. Centre for Health Economics, University of York, York, UK

4. Department of Economics and Related Studies, University of York, York, UK

5. School of Health and Related Research (ScHARR), University of Sheffield, Sheffield, UK

6. School of Social and Community Medicine, University of Bristol, Bristol, UK

7. Health Services Research Unit, Akershus University Hospital, Oslo, Norway

8. Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Canada

9. Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada

10. Department of Statistical Science, University College London, London, UK

Abstract

BackgroundExpected 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.MethodsWe 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.ResultsThe 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.ConclusionsWe 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.HighlightsExpected 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.

Funder

Canada Research Chair in Statistical Trial Design

NordForsk

Natural Sciences and Engineering Research Council of Canada

Publisher

SAGE Publications

Subject

Health Policy

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