Abstract

BackgroundAlthough Fingolimod (FGD) and Natalizumab (NTZ) appear to be effective in relapsing-remitting multiple sclerosis (RRMS), they have never been directly compared in a randomized clinical trial (RCT).Methods and FindingsWe evaluated the comparative efficacy of FGD vs. NTZ using a meta-analytical approach. Data from placebo-controlled RCTs was used for indirect comparisons and observational data was utilized for head-to-head comparisons. We identified 3 RCTs (2498 patients) and 5 observational studies (2576 patients). NTZ was associated with a greater reduction in the 2-year annualized relapse rate (ARR; SMDindirect = -0.24;95% CI: from -0.44 to -0.04; p = 0.005) and with the probability of no disease activity at 2 years (ORindirect:1.82, 95% CI: from 1.05 to 3.15) compared to FGD, while no differences between the two therapies were found in the proportion of patients who remained relapse-free (ORindirect = 1.20;95% CI: from 0.84 to 1.71) and those with disability progression (ORindirect = 0.76;95% CI: from 0.48 to 1.21) at 2 years. In the analysis of observational data, we found no significant differences between NTZ and FGD in the 2-year ARR (SMD = -0.05; 95% CI: from -0.26 to 0.16), and 2-year disability progression (OR:1.08;95% CI: from 0.77 to 1.52). However, NTZ-treated patients were more likely to remain relapse-free at 2-years compared to FGD (OR: 2.19;95% CI: from 1.15 to 4.18; p = z0.020).ConclusionsIndirect analyses of RCT data and head-to-head comparisons of observational findings indicate that NTZ may be more effective than FGD in terms of disease activity reduction in patients with RRMS. However, head-to-head RCTs are required to independently confirm this preliminary observation.

Highlights

  • Available disease modifying drugs (DMDs) have been proved to be effective in reducing disability progression in patients with relapsing remitting multiple sclerosis (RRMS) [1]

  • Indirect analyses of randomized clinical trial (RCT) data and head-to-head comparisons of observational findings indicate that NTZ may be more effective than FGD in terms of disease activity reduction in patients with RRMS

  • The second-line agents Fingolimod and Natalizumab appear to be efficacious for patients with high disease activity and generally manageable side effects [2], their comparative efficacy in patients with RRMS has never been tested within the setting of a randomized clinical trial (RCT)

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Summary

Introduction

Available disease modifying drugs (DMDs) have been proved to be effective in reducing disability progression in patients with relapsing remitting multiple sclerosis (RRMS) [1]. Highrisk RRMS patients with active or progressive disease while on treatment with a first-line agent are candidates for treatment escalation to a second-line agent, which is expected to have a more potent effect on both clinical and MRI outcomes [2]. The second-line agents Fingolimod and Natalizumab appear to be efficacious for patients with high disease activity and generally manageable side effects [2], their comparative efficacy in patients with RRMS has never been tested within the setting of a randomized clinical trial (RCT). Fingolimod (FGD) and Natalizumab (NTZ) appear to be effective in relapsingremitting multiple sclerosis (RRMS), they have never been directly compared in a randomized clinical trial (RCT)

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