Safety, immunogenicity and efficacy after switching from reference infliximab to biosimilar SB2 compared with continuing reference infliximab and SB2 in patients with rheumatoid arthritis: results of a randomised, double-blind, phase III transition study

Abstract

Objectives: Efficacy, safety and immunogenicity results from the phase III study of SB2, a biosimilar of reference infliximab (INF), were previously reported through 54 weeks. This transition period compared results in patients with rheumatoid arthritis (RA) who switched from INF to SB2 with those in patients who maintained treatment with INF or SB2.

Methods: Patients with moderate to severe RA despite methotrexate treatment were randomised (1:1) to receive SB2 or INF at weeks 0, 2 and 6 and every 8 weeks thereafter until week 46. At week 54, patients previously receiving INF were rerandomised (1:1) to switch to SB2 (INF/SB2 (n=94)) or to continue on INF (INF/INF (n=101)) up to week 70. Patients previously receiving SB2 continued on SB2 (SB2/SB2 (n=201)) up to week 70. Efficacy, safety and immunogenicity were assessed up to week 78.

Results: Efficacy was sustained and comparable across treatment groups. American College of Rheumatology (ACR) 20 responses between weeks 54 and 78 ranged from 63.5% to 72.3% with INF/SB2, 66.3%%-69.4% with INF/INF and 65.6%-68.3% with SB2/SB2. Treatment-emergent adverse events during this time occurred in 36.2%, 35.6% and 40.3%, respectively, and infusion-related reactions in 3.2%, 2.0% and 3.5%. Among patients who were negative for antidrug antibodies (ADA) up to week 54, newly developed ADAs were reported in 14.6%, 14.9% and 14.1% of the INF/SB2, INF/INF and SB2/SB2 groups, respectively.

Conclusions: The efficacy, safety and immunogenicity profiles remained comparable among the INF/SB2, INF/INF and SB2/SB2 groups up to week 78, with no treatment-emergent issues or clinically relevant immunogenicity after switching from INF to SB2.

Trial registration number: NCT01936181; EudraCT number: 2012-005733-37.

Keywords: anti-tnf; dmards (biologic); rheumatoid arthritis; tnf-alpha; treatment.

Conflict of interest statement

Competing interests: JSS reports receiving grant/research support from AbbVie, Janssen, MSD, Pfizer, Roche and UCB; consultant for AbbVie, Amgen, AstraZeneca, Astro-Pharma, Celgene, GSK, Janssen, Lilly, Medimmune, MSD, Novartis-Sandoz, Novo Nordisk, Pfizer, Roche, Samsung Bioepis, Sanofi and UCB. J-YC reports receiving grant/research support and consultant fees from Samsung Bioepis. AB reports receiving grant/research support from AbbVie and Samsung Bioepis. NP, JN, IS, ED, RY, MM, WP, HC, KJ-R and AZ report receiving grant/research support from Samsung Bioepis. YL and YHR are employees of Samsung Bioepis and own stocks in Samsung Biologics.

© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Figures

Figure 1

Patient disposition of the study population. *Percentages of patients completed and discontinued are based on the number of patients rerandomised at week 54. Note: eight patients’ data from sites in eastern Ukraine were excluded from the analysis because of regional issues (n=4 in SB2, n=4 in INF). INF, reference infliximab.

Figure 2

Mean disease activity score based on a 28-joint count (DAS28 (ESR)) (A), Clinical Disease Activity Index (CDAI) score (B) and Simplified Disease Activity Index (SDAI) score (C) up to week 78. ESR, erythrocyte sedimentation rate; INF, reference infliximab.

Figure 3

American College of Rheumatology (ACR) responses up to week 78. The responses before week 54 are retrospective analyses based on the extended full analysis set. For the actual percentages, please refer to online supplementary appendix table S2. INF, reference infliximab.

Figure 4

Incidence of immunogenicity during the transition period. *Patients having at least one positive ADA result during the transition-extension period among all patients regardless of prior ADA result up to week 54 (n=94 in INF/SB2, n=101 in INF/INF, n=201 in SB2/SB2). †Patients having at least one positive ADA result during the transition period among patients with overall negative ADA results up to week 54 (n=41 in INF/SB2, n=47 in INF/INF, n=78 in SB2/SB2). NAb was measured among ADA positive subjects (n=6, 7 and 11). ADA, antidrug antibody; NAb, neutralising antibody; INF, reference infliximab.