ArticleStatistical methods in medical research2016
Two-stage sampling designs for external validation of personal risk models.
Article in Statistical methods in medical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Assessing risk model calibration with missing covariates.Biostatistics (Oxford, England) · 2022Article
- Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors.Journal of medical genetics · 2022Article
- Prospective Evaluation of the Addition of Polygenic Risk Scores to Breast Cancer Risk Models.JNCI cancer spectrum · 2021Article
- Article
- Validation of the IBIS breast cancer risk evaluator for women with lobular carcinoma in-situ.British journal of cancer · 2018Article
- Predicting Prostate Cancer Recurrence After Radical Prostatectomy.The Prostate · 2017Article
- Practical problems with clinical guidelines for breast cancer prevention based on remaining lifetime risk.Journal of the National Cancer Institute · 2015Article
- Assessing the goodness of fit of personal risk models.Statistics in medicine · 2014Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
We propose a cost-effective sampling design and estimating procedure for validating personal risk models using right-censored cohort data. Validation involves using each subject's covariates, as ascertained at cohort entry, in a risk model (specified independently of the data) to assign him/her a probability of an adverse outcome within a future time period. Subjects are then grouped according to the magnitudes of their assigned risks, and within each group, the mean assigned risk is compared with the probability of outcome occurrence as estimated using the follow-up data. Such validation presents two complications. First, in the presence of right-censoring, estimating the probability of developing the outcomes before death requires competing risk analysis. Second, for rare outcomes, validation using the full cohort requires assembling covariates and assigning risks to thousands of subjects. This can be costly when some covariates involve analyzing biological specimens. A two-stage sampling design addresses this problem by assembling covariates and assigning risks only to those subjects most informative for estimating key parameters. We use this design to estimate the outcome probabilities needed to evaluate model performance and we provide theoretical and bootstrap estimates of their variances. We also describe how to choose two-stage designs with minimal efficiency loss for a parameter of interest when the quantities determining optimality are unknown at the time of design. We illustrate these methods by using subjects in the California Teachers Study to validate ovarian cancer risk models. We find that a design with optimal efficiency for one performance parameter need not be so for others, and trade-offs will be required. A two-stage design that samples all outcome-positive subjects and more outcome-negative than censored subjects will perform well in most circumstances. The methods are implemented in Risk Model Assessment Program, an R program freely available at http://med.stanford.edu/epidemiology/two-stage.html.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.