Matching the model with the evidence: comparing discrete event simulation and state-transition modeling for time-to-event predictions in a cost-effectiveness analysis of treatment in metastatic colorectal cancer patients

被引:19
|
作者
Degeling, Koen [1 ]
Franken, Mira D. [2 ]
May, Anne M. [3 ]
van Oijen, Martijn G. H. [4 ]
Koopman, Miriam [2 ]
Punt, Cornelis J. A. [4 ]
Ijzerman, Maarten J. [1 ]
Koffijberg, Hendrik [1 ,3 ]
机构
[1] Univ Twente, Hlth Technol & Serv Res Dept, Tech Med Ctr, POB 217, NL-7500 AE Enschede, Netherlands
[2] Univ Utrecht, Univ Med Ctr, Dept Med Oncol, Huispost B02-225,POB 85500, NL-3508 GA Utrecht, Netherlands
[3] Univ Utrecht, Univ Med Ctr, Julius Ctr Hlth Sci & Primary Care, Huispost STR 6-131,POB 85500, NL-3508 GA Utrecht, Netherlands
[4] Univ Amsterdam, Dept Med Oncol, Amsterdam UMC, POB 22660, NL-1100 DD Amsterdam, Netherlands
关键词
Markov modeling; State-transition modeling; Discrete event simulation; Time-to-event; Cost-effectiveness; Individual patient data; ECONOMIC-EVALUATION; AMERICAN SOCIETY; VALIDATION; TECHNOLOGIES;
D O I
10.1016/j.canep.2018.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Individual patient data, e.g. from clinical trials, often need to be extrapolated or combined with additional evidence when assessing long-term impact in cost-effectiveness modeling studies. Different modeling methods can be used to represent the complex dynamics of clinical practice; the choice of which may impact cost-effectiveness outcomes. We compare the use of a previously designed cohort discrete-time state-transition model (DT-STM) with a discrete event simulation (DES) model. Methods: The original DT-STM was replicated and a DES model developed using AnyLogic software. Models were populated using individual patient data of a phase III study in metastatic colorectal cancer patients, and compared based on their evidence structure, internal validity, and cost-effectiveness outcomes. The DT-STM used time-dependent transition probabilities, whereas the DES model was populated using parametric distributions. Results: The estimated time-dependent transition probabilities for the DT-STM were irregular and more sensitive to single events due to the required small cycle length and limited number of event observations, whereas parametric distributions resulted in smooth time-to-event curves for the DES model. Although the DT-STM and DES model both yielded similar time-to-event curves, the DES model represented the trial data more accurately in terms of mean health-state durations. The incremental cost-effectiveness ratio (ICER) was (sic)172,443 and (sic)168,383 per Quality Adjusted Life Year gained for the DT-STM and DES model, respectively. Conclusion: DES represents time-to-event data from clinical trials more naturally and accurately than DT-STM when few events are observed per time cycle. As a consequence, DES is expected to yield a more accurate ICER.
引用
收藏
页码:60 / 67
页数:8
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