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Randomized Controlled Trial
. 2014 Dec;73(12):2144-51.
doi: 10.1136/annrheumdis-2013-203684. Epub 2013 Aug 26.

The Canadian methotrexate and etanercept outcome study: a randomised trial of discontinuing versus continuing methotrexate after 6 months of etanercept and methotrexate therapy in rheumatoid arthritis

Janet E Pope  1 , Boulos Haraoui  2 , J Carter Thorne  3 , Andrew Vieira  4 , Melanie Poulin-Costello  4 , Edward C Keystone  5
Affiliations
Free PMC article
Randomized Controlled Trial

The Canadian methotrexate and etanercept outcome study: a randomised trial of discontinuing versus continuing methotrexate after 6 months of etanercept and methotrexate therapy in rheumatoid arthritis

Janet E Pope et al. Ann Rheum Dis. 2014 Dec.
Free PMC article

Abstract

Objective: To determine if withdrawing methotrexate (MTX) after 6 months of combination etanercept (ETN)+MTX, in MTX-inadequate responders with active rheumatoid arthritis (RA), is non-inferior to continuing ETN+MTX.

Methods: Tumour necrosis factor-inhibitor naïve RA patients with disease activity score 28 (DAS28)≥3.2, swollen joint count≥3, despite stable MTX, were treated with ETN+MTX for 6 months, followed by randomisation to either continue ETN+MTX or switch to ETN monotherapy for an additional 18 months. The primary endpoint was change in DAS28 from 6-month randomisation to 12 months. The non-inferiority margin of change in DAS28 was 0.6, with prespecified analyses (DAS28<3.2 vs DAS28≥3.2).

Results: 205 patients were randomised. DAS28 was stable in patients on ETN+MTX and increased slightly in patients on ETN monotherapy from 6 to 12 months. Non-inferiority was not achieved, with an adjusted difference of 0.4 (0.1 to 0.7) between the ETN and the ETN+MTX groups, for the month 6-12 change in DAS28. However, patients who achieved low disease activity (LDA; DAS28<3.2) at 6 months had a similar disease activity at 12 months, whether on monotherapy or combination therapy (DAS28 change 0.7 ETN vs 0.57 ETN+MTX, p=0.8148). Conversely, for patients who did not reach LDA at 6 months, those on ETN monotherapy had increased disease activity at 12 months, while disease activity continued to decrease for patients on combination therapy, at 12 months (DAS28 change 0.4 ETN vs -0.4 ETN+MTX, p=0.0023).

Conclusions: Non-inferiority was not achieved. Withdrawing MTX after 6 months of continuation ETN+MTX in MTX inadequate responders did not yield the same degree of improvement between 6 and 12 months compared with continuing ETN+MTX.

Trial registration: ClinicalTrials.gov-NCT00654368.

Keywords: Anti-TNF; DMARDs (biologic); Methotrexate; Rheumatoid Arthritis.

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Figures

Figure 1
Figure 1
(A) Study design. (B) Patient disposition to month 12.
Figure 2
Figure 2
(A) Change in disease activity score 28 (DAS28) from month 6 randomisation to month 12 (primary endpoint). (B) Change in DAS28 from month 6 randomisation to month 12—stratified by disease activity at 6 months.
Figure 3
Figure 3
Relative risk (ETN+MTX/ETN) of response from month 6 randomization to month 12.
See this image and copyright information in PMC

References

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