Minimum sample size for developing a multivariable prediction model using multinomial logistic regression

Author:

Pate Alexander1ORCID,Riley Richard D2,Collins Gary S34ORCID,van Smeden Maarten56,Van Calster Ben789ORCID,Ensor Joie2ORCID,Martin Glen P1ORCID

Affiliation:

1. Division of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

2. Centre for Prognosis Research, School of Medicine, Keele University, Staffordshire, UK

3. Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK

4. NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK

5. Julius Center for Health Sciences, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands

6. Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, Netherlands

7. Department of Development and Regeneration, KU Leuven, Leuven, Belgium

8. Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, Netherlands

9. EPI-center, KU Leuven, Leuven, Belgium

Abstract

Aims Multinomial logistic regression models allow one to predict the risk of a categorical outcome with > 2 categories. When developing such a model, researchers should ensure the number of participants ([Formula: see text]) is appropriate relative to the number of events ([Formula: see text]) and the number of predictor parameters ([Formula: see text]) for each category k. We propose three criteria to determine the minimum n required in light of existing criteria developed for binary outcomes. Proposed criteria The first criterion aims to minimise the model overfitting. The second aims to minimise the difference between the observed and adjusted [Formula: see text] Nagelkerke. The third criterion aims to ensure the overall risk is estimated precisely. For criterion (i), we show the sample size must be based on the anticipated Cox-snell [Formula: see text] of distinct ‘one-to-one’ logistic regression models corresponding to the sub-models of the multinomial logistic regression, rather than on the overall Cox-snell [Formula: see text] of the multinomial logistic regression. Evaluation of criteria We tested the performance of the proposed criteria (i) through a simulation study and found that it resulted in the desired level of overfitting. Criterion (ii) and (iii) were natural extensions from previously proposed criteria for binary outcomes and did not require evaluation through simulation. Summary We illustrated how to implement the sample size criteria through a worked example considering the development of a multinomial risk prediction model for tumour type when presented with an ovarian mass. Code is provided for the simulation and worked example. We will embed our proposed criteria within the pmsampsize R library and Stata modules.

Funder

Medical Research Council

Publisher

SAGE Publications

Subject

Health Information Management,Statistics and Probability,Epidemiology

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