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Assessing Performance and Clinical Usefulness in Prediction Models With Survival Outcomes: Practical Guidance for Cox Proportional Hazards Models

审查(临床试验) 比例危险模型 医学 预测建模 生存分析 统计 时间范围 回归分析 内科学 数学 量子力学 物理 病理
作者
David J. McLernon,Daniele Giardiello,Ben Van Calster,Laure Wynants,Nan van Geloven,Maarten van Smeden,Terry M. Therneau,Ewout W. Steyerberg,David J. McLernon,Daniele Giardiello,Ben Van Calster,Laure Wynants,Nan van Geloven,Maarten van Smeden,Terry M. Therneau,Ewout W. Steyerberg,Patrick M. Bossuyt,Tom Boyles,Gary S. Collins,Kathleen Karr,Petra Macaskill,Carl Moons,Andrew J. Vickers,Max Westphal,Michał Abrahamowicz,Malka Gorfine,Federico Ambrogi,Richard J. Cook,Jean‐Paul Gaudillière,Per Kragh Andersen,Torben Martinussen,Maja Pohar Perme,Hein Putter,Jeremy M. G. Taylor
出处
期刊:Annals of Internal Medicine [American College of Physicians]
卷期号:176 (1): 105-114 被引量:49
标识
DOI:10.7326/m22-0844
摘要

Risk prediction models need thorough validation to assess their performance. Validation of models for survival outcomes poses challenges due to the censoring of observations and the varying time horizon at which predictions can be made. This article describes measures to evaluate predictions and the potential improvement in decision making from survival models based on Cox proportional hazards regression. As a motivating case study, the authors consider the prediction of the composite outcome of recurrence or death (the “event”) in patients with breast cancer after surgery. They developed a simple Cox regression model with 3 predictors, as in the Nottingham Prognostic Index, in 2982 women (1275 events over 5 years of follow-up) and externally validated this model in 686 women (285 events over 5 years). Improvement in performance was assessed after the addition of progesterone receptor as a prognostic biomarker. The model predictions can be evaluated across the full range of observed follow-up times or for the event occurring by the end of a fixed time horizon of interest. The authors first discuss recommended statistical measures that evaluate model performance in terms of discrimination, calibration, or overall performance. Further, they evaluate the potential clinical utility of the model to support clinical decision making according to a net benefit measure. They provide SAS and R code to illustrate internal and external validation. The authors recommend the proposed set of performance measures for transparent reporting of the validity of predictions from survival models.
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