Survival Extrapolation Incorporating General Population Mortality Using Excess Hazard and Cure Models: A Tutorial

被引:6
|
作者
Sweeting, Michael J. [1 ,7 ]
Rutherford, Mark J. [2 ]
Jackson, Dan [1 ]
Lee, Sangyu [2 ]
Latimer, Nicholas R. [3 ,4 ]
Hettle, Robert [5 ]
Lambert, Paul C. [2 ,6 ]
机构
[1] AstraZeneca, Stat Innovat, Cambridge, England
[2] Univ Leicester, Dept Populat Hlth Sci, Leicester, England
[3] Univ Sheffield, Sch Hlth & Related Res, Sheffield, England
[4] Delta Hat Ltd, Nottingham, England
[5] AstraZeneca, Hlth Econ & Payer Evidence, Cambridge, England
[6] Karolinska Inst, Dept Med Epidemiol & Biostat, Solna, Sweden
[7] AstraZeneca, Stat Innovat, City House,Hills Rd, Cambridge CB2 1RY, England
关键词
survival extrapolation; health technology assessment; excess hazard models; modeling; overall survival; FRACTION; CANCER;
D O I
10.1177/0272989X231184247
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Different parametric survival models can lead to widely discordant extrapolations and decision uncertainty in cost-effectiveness analyses. The use of excess hazard (EH) methods, which incorporate general population mortality data, has the potential to reduce model uncertainty. This review highlights key practical considerations of EH methods for estimating long-term survival. Methods Demonstration of methods used a case study of 686 patients from the German Breast Cancer Study Group, followed for a maximum of 7.3 y and divided into low (1/2) and high (3) grade cancers. Seven standard parametric survival models were fit to each group separately. The same 7 distributions were then used in an EH framework, which incorporated general population mortality rates, and fitted both with and without a cure parameter. Survival extrapolations, restricted mean survival time (RMST), and difference in RMST between high and low grades were compared up to 30 years along with Akaike information criterion goodness-of-fit and cure fraction estimates. The sensitivity of the EH models to lifetable misspecification was investigated. Results In our case study, variability in survival extrapolations was extensive across the standard models, with 30-y RMST ranging from 7.5 to 14.3 y. Incorporation of general population mortality rates using EH cure methods substantially reduced model uncertainty, whereas EH models without cure had less of an effect. Long-term treatment effects approached the null for most models but at varying rates. Lifetable misspecification had minimal effect on RMST differences. Conclusions EH methods may be useful for survival extrapolation, and in cancer, EHs may decrease over time and be easier to extrapolate than all-cause hazards. EH cure models may be helpful when cure is plausible and likely to result in less extrapolation variability.
引用
收藏
页码:737 / 748
页数:12
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