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      Real-World Observational Evaluation of Hair Thinning in Patients with Multiple Sclerosis Receiving Teriflunomide: Is It an Issue in Clinical Practice?

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          Abstract

          Introduction

          Hair thinning occurred in 10–14% of teriflunomide-treated patients in the teriflunomide multiple sclerosis clinical development program, compared with 5% of placebo-treated patients. Our objective was to examine the clinical course of hair thinning in patients in an observational real-world project.

          Methods

          Patients with relapsing–remitting multiple sclerosis who reported hair thinning to healthcare professionals (HCPs) during treatment with teriflunomide were eligible for inclusion. During two office visits, one at onset of hair thinning and another at follow-up, HCPs and patients completed questionnaires that categorized hair thinning as mild, moderate, or severe, or from 0 (no hair thinning) to 10 (very severe hair thinning), respectively. At the follow-up visit, patients also rated the degree of recovery. Patients were photographed at both visits with a standardized protocol and camera.

          Results

          Of the 38 patients who completed follow-up, most were women (97%) without prior history of hair thinning (87%), with the majority (68%) receiving concomitant medications potentially associated with hair thinning. The mean time to onset of hair thinning was 77 days after the first teriflunomide dose. HCPs classified the majority of hair thinning events as mild (63%) or moderate (34%), with one event classified as severe (3%). The mean patient severity perception was 5/10, and complete/near-complete resolution or marked improvement was reported by 79% of patients.

          Conclusion

          Consistent with observations from the teriflunomide clinical program, hair thinning was usually mild and occurred within the first 3 months of treatment, with most patients fully recovering while remaining on teriflunomide treatment. As with any potential adverse event, it is important to ensure appropriate expectations through patient education before treatment.

          Funding

          Sanofi.

          Related collections

          Most cited references10

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          Multiple sclerosis: side effects of interferon beta therapy and their management.

          Article abstract-Interferon beta (IFNbeta) reduces the relapse rate, disease activity as measured by serial MRI scanning, and disease progression of MS. Therapy with IFNbeta may be associated with a number of adverse reactions. Relatively frequent side effects include flu-like symptoms, transient laboratory abnormalities, menstrual disorders, and increased spasticity. Dermal injection site reactions occur after subcutaneous application of IFNbeta-1b and IFNbeta-1a. Possible side effects of IFNbeta include various autoimmune reactions, capillary leak syndrome, anaphylactic shock, thrombotic-thrombocytopenic purpura, insomnia, headache, alopecia, and depression. We discuss the mechanisms and management of the different side effects of IFNbeta.
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            Is Open Access

            Pooled safety and tolerability data from four placebo-controlled teriflunomide studies and extensions.

            Teriflunomide, a once-daily oral immunomodulator for the treatment of relapsing-remitting multiple sclerosis, has demonstrated consistent efficacy on clinical and MRI parameters in clinical trials.
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              Is Open Access

              Alopecia Universalis following Alemtuzumab Treatment in Multiple Sclerosis: A Barely Recognized Manifestation of Secondary Autoimmunity—Report of a Case and Review of the Literature

              Secondary autoimmunity is the most frequent adverse event occurring in almost every other alemtuzumab-treated multiple sclerosis patient. We report a case of a patient with relapsing-remitting multiple sclerosis who reported smooth, circular areas of complete hair loss on both thighs 6 months after the second treatment cycle with alemtuzumab. The patient was diagnosed as having alopecia areata (AA). Within 3 months, AA progressed to complete loss of all body hair (alopecia universalis). Current literature rarely connects alemtuzumab with the onset of alopecia of autoimmune origin. Here, we report a little-noticed autoimmune disease affecting the skin, very likely being associated with alemtuzumab. We emphasize the necessity of careful clinical surveillance of alemtuzumab-treated patients for yet undescribed autoimmune diseases.
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                Author and article information

                Contributors
                LHT@pnal.net
                Journal
                Neurol Ther
                Neurol Ther
                Neurology and Therapy
                Springer Healthcare (Cheshire )
                2193-8253
                2193-6536
                6 August 2018
                6 August 2018
                December 2018
                : 7
                : 2
                : 341-347
                Affiliations
                [1 ]ISNI 0000 0004 4902 6818, GRID grid.492926.2, Phoenix Neurological Associates Ltd, ; Phoenix, AZ USA
                [2 ]Multiple Sclerosis Treatment Center of Dallas, Dallas, TX USA
                [3 ]ISNI 0000 0000 8814 392X, GRID grid.417555.7, Sanofi, ; Cambridge, MA USA
                [4 ]GRID grid.477644.2, Multiple Sclerosis Center of Northeastern New York, ; Latham, NY USA
                Article
                107
                10.1007/s40120-018-0107-y
                6283787
                30084001
                fc8bff88-0451-4a54-be2d-86badf85bf56
                © The Author(s) 2018
                History
                : 8 May 2018
                Funding
                Funded by: FundRef https://dx.doi.org/10.13039/100004339, Sanofi;
                Categories
                Original Research
                Custom metadata
                © The Author(s) 2018

                multiple sclerosis,real-world data,safety,teriflunomide
                multiple sclerosis, real-world data, safety, teriflunomide

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