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Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry

BACKGROUND: The association between multiple sclerosis and malignancy is controversial and a current appraisal is needed. OBJECTIVE: To determine the incidence of malignancy in patients with multiple sclerosis compared with the general population and in relation to disease-modifying therapy. METHODS...

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Autores principales: Nørgaard, Mette, Veres, Katalin, Sellebjerg, Finn T, Svingel, Lise S, Foch, Caroline, Boutmy, Emmanuelle, Sabidó, Meritxell, Magyari, Melinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613897/
https://www.ncbi.nlm.nih.gov/pubmed/34840804
http://dx.doi.org/10.1177/20552173211053939
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author Nørgaard, Mette
Veres, Katalin
Sellebjerg, Finn T
Svingel, Lise S
Foch, Caroline
Boutmy, Emmanuelle
Sabidó, Meritxell
Magyari, Melinda
author_facet Nørgaard, Mette
Veres, Katalin
Sellebjerg, Finn T
Svingel, Lise S
Foch, Caroline
Boutmy, Emmanuelle
Sabidó, Meritxell
Magyari, Melinda
author_sort Nørgaard, Mette
collection PubMed
description BACKGROUND: The association between multiple sclerosis and malignancy is controversial and a current appraisal is needed. OBJECTIVE: To determine the incidence of malignancy in patients with multiple sclerosis compared with the general population and in relation to disease-modifying therapy. METHODS: Patients with multiple sclerosis (1995 – 2015) were matched by birth year and sex to individuals without multiple sclerosis in the general population. Patients with multiple sclerosis initiating disease-modifying therapy were evaluated using landmark period analysis. Malignancy risk was assessed by incidence rates, incidence rate ratios, and standardised incidence ratios. RESULTS: The standardised incidence ratio of any malignancy (excluding non-melanoma skin cancer) in patients with multiple sclerosis (n = 10,557) was 0.96 (95% CI 0.88 – 1.06), and there was no increased incidence of specific malignancy types compared with the general population cohort (n = 103,761). At the 48-month landmark period, the age-adjusted incidence per 100,000 person-years of any malignancy (excluding non-melanoma skin cancer) was 436.7 (95% CI 361.0 – 512.4) in patients newly treated with immunomodulator-only and 675.1 (95% CI 130.4 – 1219.9) in patients newly treated with immunosuppressant-only. CONCLUSIONS: There was no increased incidence of malignancy overall or by type in patients with multiple sclerosis compared neither with the general population nor in relation to disease-modifying therapy.
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spelling pubmed-86138972021-11-26 Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry Nørgaard, Mette Veres, Katalin Sellebjerg, Finn T Svingel, Lise S Foch, Caroline Boutmy, Emmanuelle Sabidó, Meritxell Magyari, Melinda Mult Scler J Exp Transl Clin Original Research Article BACKGROUND: The association between multiple sclerosis and malignancy is controversial and a current appraisal is needed. OBJECTIVE: To determine the incidence of malignancy in patients with multiple sclerosis compared with the general population and in relation to disease-modifying therapy. METHODS: Patients with multiple sclerosis (1995 – 2015) were matched by birth year and sex to individuals without multiple sclerosis in the general population. Patients with multiple sclerosis initiating disease-modifying therapy were evaluated using landmark period analysis. Malignancy risk was assessed by incidence rates, incidence rate ratios, and standardised incidence ratios. RESULTS: The standardised incidence ratio of any malignancy (excluding non-melanoma skin cancer) in patients with multiple sclerosis (n = 10,557) was 0.96 (95% CI 0.88 – 1.06), and there was no increased incidence of specific malignancy types compared with the general population cohort (n = 103,761). At the 48-month landmark period, the age-adjusted incidence per 100,000 person-years of any malignancy (excluding non-melanoma skin cancer) was 436.7 (95% CI 361.0 – 512.4) in patients newly treated with immunomodulator-only and 675.1 (95% CI 130.4 – 1219.9) in patients newly treated with immunosuppressant-only. CONCLUSIONS: There was no increased incidence of malignancy overall or by type in patients with multiple sclerosis compared neither with the general population nor in relation to disease-modifying therapy. SAGE Publications 2021-11-23 /pmc/articles/PMC8613897/ /pubmed/34840804 http://dx.doi.org/10.1177/20552173211053939 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Nørgaard, Mette
Veres, Katalin
Sellebjerg, Finn T
Svingel, Lise S
Foch, Caroline
Boutmy, Emmanuelle
Sabidó, Meritxell
Magyari, Melinda
Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title_full Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title_fullStr Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title_full_unstemmed Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title_short Incidence of malignancy in multiple sclerosis: A cohort study in the Danish Multiple Sclerosis Registry
title_sort incidence of malignancy in multiple sclerosis: a cohort study in the danish multiple sclerosis registry
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613897/
https://www.ncbi.nlm.nih.gov/pubmed/34840804
http://dx.doi.org/10.1177/20552173211053939
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