Evidence map›Paper›PMID 34706759›Full record

ArticleDiagnostic and prognostic research2021

Development, validation and clinical usefulness of a prognostic model for relapse in relapsing-remitting multiple sclerosis.

Konstantina Chalkou, Ewout Steyerberg, Patrick Bossuyt, Suvitha Subramaniam, Pascal Benkert, Jens Kuhle, Giulio Disanto, Ludwig Kappos, Chiara Zecca, Matthias Egger and 1 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostic and prognostic research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Konstantina ChalkouInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland. konstantina.chalkou@ispm.unibe.ch.ORCID http://orcid.org/0000-0001-9718-021X
Ewout SteyerbergLeiden University Medical Center, Leiden, the Netherlands.
Patrick BossuytDepartment Epidemiology and Data Science, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, the Netherlands.
Suvitha SubramaniamClinical Trial Unit, Department of Clinical Research,, University Hospital Basel, University of Basel, Basel, Switzerland.
Pascal BenkertClinical Trial Unit, Department of Clinical Research,, University Hospital Basel, University of Basel, Basel, Switzerland.
Jens KuhleMultiple Sclerosis Centre, Neurologic Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, Biomedicine and Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
Giulio DisantoNeurocenter of Southern Switzerland, Civic Hospital, Lugano, Switzerland.
Ludwig KapposMultiple Sclerosis Centre, Neurologic Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, Biomedicine and Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
Chiara ZeccaMultiple Sclerosis Center, Neurocenter of Southern Switzerland, EOC, Lugano, Switzerland.
Matthias EggerInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Georgia SalantiInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
University of Basel · CHUniversity of Bern · CHLaboratory for Biomedical Neurosciences · CHLeiden University Medical Center · NLUniversity of Amsterdam · NL

Funding

European Union's Horizon 2020 No 825162
6 · The paper itself

Abstract

backgroundPrognosis for the occurrence of relapses in individuals with relapsing-remitting multiple sclerosis (RRMS), the most common subtype of multiple sclerosis (MS), could support individualized decisions and disease management and could be helpful for efficiently selecting patients for future randomized clinical trials. There are only three previously published prognostic models on this, all of them with important methodological shortcomings.

objectivesWe aim to present the development, internal validation, and evaluation of the potential clinical benefit of a prognostic model for relapses for individuals with RRMS using real-world data.

methodsWe followed seven steps to develop and validate the prognostic model: (1) selection of prognostic factors via a review of the literature, (2) development of a generalized linear mixed-effects model in a Bayesian framework, (3) examination of sample size efficiency, (4) shrinkage of the coefficients, (5) dealing with missing data using multiple imputations, (6) internal validation of the model. Finally, we evaluated the potential clinical benefit of the developed prognostic model using decision curve analysis. For the development and the validation of our prognostic model, we followed the TRIPOD statement.

resultsWe selected eight baseline prognostic factors: age, sex, prior MS treatment, months since last relapse, disease duration, number of prior relapses, expanded disability status scale (EDSS) score, and number of gadolinium-enhanced lesions. We also developed a web application that calculates an individual's probability of relapsing within the next 2 years. The optimism-corrected c-statistic is 0.65 and the optimism-corrected calibration slope is 0.92. For threshold probabilities between 15 and 30%, the "treat based on the prognostic model" strategy leads to the highest net benefit and hence is considered the most clinically useful strategy.

conclusionsThe prognostic model we developed offers several advantages in comparison to previously published prognostic models on RRMS. Importantly, we assessed the potential clinical benefit to better quantify the clinical impact of the model. Our web application, once externally validated in the future, could be used by patients and doctors to calculate the individualized probability of relapsing within 2 years and to inform the management of their disease.

Indexed as

Clinical benefitClinical usefulnessPrognosisPrognostic modelRelapsing-remitting multiple sclerosis

Identifiers

PMID34706759
PMCPMC8549310
OpenAlexW3161546710

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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.