Biomarkers of Remission in Rheumatoid Arthritis (BioRRA)

Newcastle-upon-Tyne Hospitals NHS Trust

Status: Completed

Conditions: Rheumatoid Arthritis

Treatments: Drug: DMARD cessation

Study type: Interventional

Funder types: Other

Identifiers

NCT02219347

NUTH7100

Details and patient eligibility

About

Rheumatoid arthritis is a common condition affecting approximately 1% of the United Kingdom population; it is an autoimmune disease where the body's natural defences (the immune system) attack the body itself resulting, most notably, in joint damage and arthritis. To help prevent this, patients with rheumatoid arthritis need to take disease-modifying anti-rheumatic drugs (DMARDs). As rheumatoid arthritis is a life-long condition, these drug treatments are prescribed as long-term medications taken for many years.

With successful drug treatment, many patients are able to achieve an excellent control of their disease and their arthritis can go in to remission. At present, there are no markers which can reliably predict which of these patients can reduce their drug treatment, and hence benefit from a lower risk of side effects and inconvenience, without an increase in their arthritis activity.

We invite patients with stable rheumatoid arthritis to participate in this study conducted by Newcastle upon Tyne Hospitals NHS Foundation Trust in collaboration with Newcastle University and funded by the Wellcome Trust. Patients whose arthritis is confirmed as being in remission will be able to stop their DMARD medication and be monitored for a period of 6 months. Patients whose arthritis activity increases during this time will be able to restart their DMARD medication, whereas those patients whose arthritis remains in remission will be able to stay off DMARD medication.

The main aim of this study is to identify clinical, ultrasound and blood markers that can predict which patients will remain in remission after stopping DMARD medication. If identified, these markers could be a useful guide to doctors and patients in the future when deciding whether to stop DMARD therapy.

Enrollment: 74 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Clinical diagnosis of rheumatoid arthritis made by consultant rheumatologist at least 12 months previously
• Current single or combination use of methotrexate, sulphasalazine and/or hydroxychloroquine
• Arthritis currently in remission, as judged clinically by referring healthcare professional
• Willing to consider DMARD withdrawal

Exclusion criteria

• Use of biologic therapy within the past 6 months
• Received steroids within past 3 months (enteral, parenteral or intra-articular)
• Use of any DMARD other than methotrexate, sulphasalazine or hydroxychloroquine within the past 6 months (or past 12 months for leflunomide)
• Current pregnancy, or pregnancy planned within next 6 months
• Current participation within another clinical trial
• Inability to provide informed consent

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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74 participants in 1 patient group

DMARD cessation

Other group

Description:

All patients recruited to the study who have a Disease Activity in 28 Joints C-Reactive Protein (DAS28-CRP) score of \< 2.4 and who do not have power Doppler synovitis on a 7-joint musculoskeletal ultrasound scan will stop their DMARD therapy. These patients will then be followed-up for a period of 6 months or until flare of their arthritis activity, whichever is sooner.

Treatment:

Drug: DMARD cessation