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Cancer diagnosis in a Spanish cohort of multiple sclerosis patients under dimethylfumarate treatment.

作者信息

Gómez-Moreno Mayra, Sánchez-Seco Victoria Galán, Moreno-García Sara, Cámara Paula Salgado, Sabin-Muñoz Julia, Ayuso-Peralta Lucia, Oreja-Guevara Celia, Díaz-Díaz Judit, Sainz de la Maza Susana, Costa-Frossard Lucienne, Pilo de la Fuente Belén, Aladro-Benito Yolanda

机构信息

Department of Neurology, Hospital Universitario Infanta Leonor, Avenida Gran Vía del Este, 80, 28031 Madrid, Spain.

Multiple Sclerosis Unit, Department of Neurology, Hospital Universitario Doce de Octubre, Av. de Córdoba, s/n, 28041 Madrid, Spain.

出版信息

Mult Scler Relat Disord. 2021 Apr;49:102747. doi: 10.1016/j.msard.2021.102747. Epub 2021 Jan 11.

Abstract

BACKGROUND

Potential increase of cancer incidence is one of the main safety concerns of the disease-modifying therapies employed in Multiple Sclerosis (MS).

OBJECTIVE

Detailed description of patients who developed cancer among a prospective cohort of Spanish MS patients on dimethyl fumarate (DMF) treatment.

METHODS

We describe patients who developed cancer among a cohort of 886 MS patients on DMF treatment (2681 patient-years), with a median time of exposure of 39.5 months (IQR 23-51.5), who participated in a multicentre and prospective real-world study conducted in 16 Spanish National Health System hospitals from February 2014 to May 2019. Local researchers were periodically contacted by the investigation team to monitor safety issues. Cancer histories were collected from the medical records and the information was updated at July 30 2020.

RESULTS

Eight Caucasian women developed cancer, which accounts for 0.9% and an accumulated malignancy rate of 298.39 cases per 100,000 patient-years of DMF exposure. At the time of cancer diagnosis, age was between 33 to 67 years and median time on DMF treatment 16.5 months (range 1-53). Two patients had familiar history of cancer. No specific cancer lines were found (breast cancer in 2 cases, thyroid in 3, urothelial carcinoma, cervix and a progression to leiomyosarcoma from a mitotically active leiomyoma). DMF was withdrawn during cancer treatment in 6 patients and reintroduced later. All cancers except one are in complete remission. The patient with leiomyosarcoma died by cancer progression.

CONCLUSION

A relationship between cancers and DMF is unlikely because the malignancy rate was similar to that of the age-and sex-matched general population, and because of the absence of specific tumour cell lines. Nevertheless, as with other immunosuppressive DMTs, clinicians treating MS should be aware of any potential cancer symptom and demand proper testing.

摘要

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