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   <subfield code="a">Cancer and multiple sclerosis in the era of disease-modifying treatments</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Christine Lebrun, Patrick Vermersch, David Brassat, Gilles Defer, Lucien Rumbach, Pierre Clavelou, Marc Debouverie, Jérôme de Seze, Sandrine Wiertlevsky, Olivier Heinzlef, Ayman Tourbah, Agnes Fromont, Marc Frenay]</subfield>
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   <subfield code="a">Prior to the era of disease-modifying therapies (DMT), multiple sclerosis (MS) was linked to reduced rates of cancer. Early use of immunosuppressors (IS) in MS justifies the follow-up of patients to evaluate a possible increase in the incidence of cancer in these patients. We performed a descriptive study of MS patients with a documented oncological event. Among the 22,563 MS patients in the EDMUS databases, patients with a history of cancer were identified, and cancer risk in a multiple sclerosis cohort (CARIMS) was evaluated. Four groups were defined: (A) MS patients without cancer receiving DMT or not, (B) MS patients with cancer but without any history of DMT, (C) MS patients with cancer who received an immunomodulator (IM), and/or (D) MS patients treated with an IS. A total of 9,269 patients (44.1%) had a history of DMT (52% IM; 18% IS; 30% both); 253 patients with MS and cancer were identified, 182 had a history of DMT. The mean duration of DMT was longer for group D (A: 3.6years vs. D: 4.9years; P&lt;0.01). There was no increased risk of cancer among patients treated exclusively with IM. IS treatment (P=0.043) and the duration of exposure (P&lt;0.001) significantly increased the risk of cancer, especially skin cancer, as observed in other autoimmune diseases. This result could influence the attitude of the medical profession with respect to the benefit to risk ratio when proposing DMT to MS patients.</subfield>
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   <subfield code="a">Cancer</subfield>
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   <subfield code="a">Multiple sclerosis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Immunosuppressive drug therapies</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Interferon beta</subfield>
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   <subfield code="a">Lebrun</subfield>
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   <subfield code="u">Service de Neurologie, CHU Pasteur, 30 voie romaine, 06002, Nice, France</subfield>
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   <subfield code="a">Vermersch</subfield>
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   <subfield code="u">Service de Neurologie, CHU Purpan, Toulouse, France</subfield>
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   <subfield code="a">Defer</subfield>
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   <subfield code="u">Service de Neurologie, CHU Côte de Nacre, Caen, France</subfield>
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   <subfield code="u">Service de Neurologie, CHU Minjoz, Besançon, France</subfield>
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   <subfield code="u">Service de Neurologie, CHU Montpied, Clermont-Ferrand, France</subfield>
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   <subfield code="a">Wiertlevsky</subfield>
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   <subfield code="a">Heinzlef</subfield>
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   <subfield code="a">Tourbah</subfield>
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   <subfield code="u">Service de Neurologie, CHU Reims, Reims, France</subfield>
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   <subfield code="a">Fromont</subfield>
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   <subfield code="u">Service de Neurologie, CHU Dijon, Dijon, France</subfield>
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   <subfield code="a">Frenay</subfield>
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   <subfield code="u">Oncologie Médicale, Pharmacologie Clinique, Nice, France</subfield>
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   <subfield code="t">Journal of Neurology</subfield>
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   <subfield code="g">258/7(2011-07-01), 1304-1311</subfield>
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