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Framework for personalized prediction of treatment response in relapsing-remitting multiple sclerosis: a replication study in independent data.
Sakr, Anna Maria; Mansmann, Ulrich; Havla, Joachim; Ön, Begum Irmak; Ön, Begum Irmak.
  • Sakr AM; Institute for Medical Information Processing, Biometry and Epidemiology (IBE), Faculty of Medicine, LMU Munich, Marchioninistrasse 15, Munich, 81377, Germany. anna.sakr@ibe.med.uni-muenchen.de.
  • Mansmann U; Pettenkofer School of Public Health, Elisabeth-Winterhalter-Weg 6, Munich, 81377, Germany. anna.sakr@ibe.med.uni-muenchen.de.
  • Havla J; Institute for Medical Information Processing, Biometry and Epidemiology (IBE), Faculty of Medicine, LMU Munich, Marchioninistrasse 15, Munich, 81377, Germany.
  • Ön BI; Pettenkofer School of Public Health, Elisabeth-Winterhalter-Weg 6, Munich, 81377, Germany.
  • Ön BI; Institute of Clinical Neuroimmunology, University Hospital, LMU Munich, Marchioninistrasse 15, Munich, 81377, Germany.
BMC Med Res Methodol ; 24(1): 138, 2024 Jun 24.
Article en En | MEDLINE | ID: mdl-38914938
ABSTRACT

BACKGROUND:

Individualizing and optimizing treatment of relapsing-remitting multiple sclerosis patients is a challenging problem, which would benefit from a clinically valid decision support. Stühler et al. presented black box models for this aim which were developed and internally evaluated in a German registry but lacked external validation.

METHODS:

In patients from the French OFSEP registry, we independently built and validated models predicting being free of relapse and free of confirmed disability progression (CDP), following the methodological roadmap and predictors reported by Stühler. Hierarchical Bayesian models were fit to predict the outcomes under 6 disease-modifying treatments given the individual disease course up to the moment of treatment change. Data was temporally split on 2017, and models were developed in patients treated earlier (n = 5517). Calibration curves, discrimination, mean squared error (MSE) and relative percentage of root MSE (RMSE%) were assessed by external validation of models in more-recent patients (n = 3768). Non-Bayesian fixed-effects GLMs were also applied and their outcomes were compared to these of the Bayesian ones. For both, we modelled the number of on-therapy relapses with a negative binomial distribution, and CDP occurrence with a binomial distribution.

RESULTS:

The performance of our temporally-validated relapse model (MSE 0.326, C-Index 0.639) is potentially superior to that of Stühler's (MSE 0.784, C-index 0.608). Calibration plots revealed miscalibration. Our CDP model (MSE 0.072, C-Index 0.777) was also better than its counterpart (MSE 0.131, C-index 0.554). Results from non-Bayesian fixed-effects GLM models were similar to the Bayesian ones.

CONCLUSIONS:

The relapse and CDP models rebuilt and externally validated in independent data could compare and strengthen the credibility of the Stühler models. Their model-building strategy was replicable.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes / Esclerosis Múltiple Recurrente-Remitente / Medicina de Precisión Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes / Esclerosis Múltiple Recurrente-Remitente / Medicina de Precisión Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article