Abstract

Introduction: We have different treatment alternatives for relapsing-remitting multiple sclerosis–RRMS–within the so-called platform drugs. It would be desirable to know the ideal drug for each patient. Real clinical practice studies provide us with data on drug efficacy in the medium and long term, safety beyond clinical trials, and can help us to know the patient profile appropriate for each therapy.Material and Methods: An observational multicenter study of real clinical practice in patients with RRMS who were treated with teriflunomide in the Valencian Community, since teriflunomide was authorized in Spain. The database created for this study collects retrospectively patients followed prospectively in the MS clinics.Objectives: To analyze the efficacy and safety of teriflunomide treatment in patients with RRMS under the conditions of real clinical practice, and to identify a patient profile responding to the treatment.Results: We obtained data from 340 patients who received at least one dose of 14 mg teriflunomide. The patients were 69.4% female to 30.6% male, had a mean age of 46.4 years, and a mean time of progression of MS of 11.5 years. The mean pre-teriflunomide relapse rate was 0.4 years, the mean EDSS scorewas 1.98, IgG Oligoclonal bands were present in the CSF of 66.2% of the patients, IgM Oligoclonal bands were present in 46.9%, and the mean number of gadolinium-enhancing lesions was 1.07 lesions per patient at the beginning of treatment. The average number of treatments previously received was 1.04, and 28.53% were naïve. After a follow-up of up to 4 years, a reduction in the annualized and cumulative annualized relapse rate was observed in the first year, in the second year, and in the third year, compared to the pre-treatment year. The EDSS scores were stabilized throughout the follow-up. Likewise, there was a reduction in gadolinium-enhancing lesions in the 1st and 2nd years compared to the pre-treatment period. Applying different generalized multiple linear regression models, we identified a profile of a responding patient to teriflunomide as a male without IgM oligoclonal bands in the CSF, a previous EDSS score of <3, and more than 5 years duration of MS.

Highlights

  • We have different treatment alternatives for relapsing-remitting multiple sclerosis–RRMS–within the so-called platform drugs

  • The other 3 were causes of withdrawal: there were an ovarian neoplasm, a breast neoplasm, and a malign glioma. This is an observational study of real clinical practice that analyzes patients diagnosed with RRMS who have been treated with teriflunomide in 7 units and monographic clinics of demyelinating diseases

  • Real clinical practice studies provide us with data on the efficacy of different treatments in the medium and long term, safety beyond clinical trials, and can help us to know the patient profile appropriate for each therapy; especially when we have a great number of therapies to be used in RRMS patients

Read more

Summary

Introduction

We have different treatment alternatives for relapsing-remitting multiple sclerosis–RRMS–within the so-called platform drugs. Real clinical practice studies provide us with data on drug efficacy in the medium and long term, safety beyond clinical trials, and can help us to know the patient profile appropriate for each therapy. Since January 2015, there are two new oral drugs available in Spain for the initial treatment of relapsing-remitting multiple sclerosis: teriflunomide and dimethyl fumarate. When the patients switched to oral therapies, the following questions were raised. Real clinical practice studies provide us with data on efficacy in the medium and long term, safety beyond clinical trials, and may help us to know the patient profile appropriate for each therapy. Real clinical practice studies aim to answer these questions, providing information on long-term efficacy, new or unexpected adverse events, and other data about some MS aspects like persistence or adherence

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.