Abstract Immunomodulatory drugs (IMiDs) may favour autoimmune diseases (ADs) occurrence. We conducted a retrospective study to evaluate ADs occurrence among IMIDs-treated myeloma patients. Patients were grouped into three classes depending on the type of IMID used. The first group included patients treated with thalidomide (Thal) (n=474), the second group with lenalidomide (Len) (n=140), while patients in the third group were first treated with Thal followed by Len (Thal-Len) (n= 94). Absolute risk of AD was 0.4% for patients treated with Thal, 4.3% for Len, and 1.1% for Thal-Len group. ADs manifested prevalently as autoimmune cytopenias (55%), although we observed one vasculitis, one optic neuritis, one Grave's disease, and one polymiositis. ADs occurred preferentially in the first months of IMiD treatment. A previous autologous transplant was shown to be a significant risk factor. All ADs were managed with IMiD discontinuation and steroids, resolving in few weeks, except for Grave's disease and polymiositis
Autoimmune diseases during treatment with immunomodulatory drugs in multiple myeloma: selective occurrence after lenalidomide / V. Montefusco, M. Galli, F. Spina, P. Stefanoni, A. Mussetti, G. Perrone, C. De Philippis, S. Dalto, F. Maura, C. Bonini, F. Rezzonico, M. Pennisi, L. Roncari, M. Soldarini, A. Dodero, L. Farina, F. Cocito, C. Caprioli, P. Corradini. - In: LEUKEMIA & LYMPHOMA. - ISSN 1042-8194. - 55:9(2014), pp. 2032-2037. [10.3109/10428194.2014.914203]
Autoimmune diseases during treatment with immunomodulatory drugs in multiple myeloma: selective occurrence after lenalidomide
P. CorradiniUltimo
2014
Abstract
Abstract Immunomodulatory drugs (IMiDs) may favour autoimmune diseases (ADs) occurrence. We conducted a retrospective study to evaluate ADs occurrence among IMIDs-treated myeloma patients. Patients were grouped into three classes depending on the type of IMID used. The first group included patients treated with thalidomide (Thal) (n=474), the second group with lenalidomide (Len) (n=140), while patients in the third group were first treated with Thal followed by Len (Thal-Len) (n= 94). Absolute risk of AD was 0.4% for patients treated with Thal, 4.3% for Len, and 1.1% for Thal-Len group. ADs manifested prevalently as autoimmune cytopenias (55%), although we observed one vasculitis, one optic neuritis, one Grave's disease, and one polymiositis. ADs occurred preferentially in the first months of IMiD treatment. A previous autologous transplant was shown to be a significant risk factor. All ADs were managed with IMiD discontinuation and steroids, resolving in few weeks, except for Grave's disease and polymiositisFile | Dimensione | Formato | |
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