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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.
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页码:60 / 67
页数:8
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