Evaluation of 200 mg of Rituximab Every 6 Months as Maintenance Treatment of Rituximab-treated Patients With Rheumatoid Arthritis

Rheumatoid arthritis (RA) is the most prevalent chronic inflammatory rheumatic disease in Europe, affecting 0.3%-0.5% of the population. Treatment follows a Treat-to-Target (T2T) approach, where patients are initially managed with conventional synthetic DMARDs (csDMARDs), such as methotrexate, and if necessary, escalated to biologic DMARDs (bDMARDs) like Rituximab, a monoclonal antibody that depletes CD20-positive B cells.

The current standard maintenance therapy for RA patients receiving Rituximab consists of 1g infusions every six months. However, concerns about long-term safety, immune suppression, and cost have led researchers to explore lower doses. Studies suggest that 200 mg of Rituximab may be sufficient to maintain disease control while potentially reducing the risks associated with B-cell depletion, such as hypogammaglobulinemia and serious infections.

Study Rationale and Objectives The RADAR trial aims to provide definitive evidence on the feasibility of reducing Rituximab doses without compromising efficacy. A previous randomized trial indicated that a 500 mg dose was non-inferior to 1g, but the 200 mg arm lacked sufficient statistical power. Subsequent long-term follow-up data suggest that 200 mg may also be effective, warranting further investigation.

The primary objective of this study is to demonstrate that the 200 mg Rituximab maintenance dose is non-inferior to 1g in terms of disease activity, measured by DAS28-CRP at 12 months.

Secondary objectives include:

• Comparing disease activity at 6 and 12 months
• Evaluating treatment failure rates (need for additional Rituximab doses, switching to other bDMARDs, corticosteroid use)
• Assessing flare occurrence and patient-reported outcomes (quality of life, disability index)
• Investigating B and T lymphocyte subpopulations and immunoglobulin levels (IgG, IgA, IgM)
• Analyzing vaccine responses and Human Anti-Chimeric Antibody (HACA) levels
• Monitoring immunosuppression markers, such as Torque Teno Virus (TTV) viral load
• Documenting adverse and serious adverse events Study Design

This is a multicenter, double-blinded, non-inferiority, randomized controlled trial (RCT). Patients will be randomized 1:1 to receive either:

• 200 mg of Rituximab (experimental group)
• 1g of Rituximab (control group) Participants will receive two infusions: one at baseline (Month 0) and one at 6 months, with follow-up visits at 4, 6, 10, and 12 months. The primary endpoint is the mean reduction in DAS28-CRP between baseline and 12 months.

Blinding Procedure:

• Infusions will be prepared in the central pharmacy to ensure identical appearance in both groups.
• Neither patients nor clinicians will know the assigned dosage.

Inclusion criteria

• Adults (≥18 years) with RA (EULAR/ACR 2010 criteria)
• Low disease activity (DAS28-CRP <3.2) on Rituximab
• Prior treatment with Rituximab (at least one infusion in the past year)
• Stable on csDMARDs (if applicable)
• Corticosteroid dose ≤10 mg/day

Non-inclusion criteria:

• Autoimmune diseases other than RA
• Severe infections, immunodeficiency, or uncontrolled disease
• Active or untreated tuberculosis, hepatitis B/C
• Pregnancy, breastfeeding, or planned pregnancy
• Drug/alcohol addiction
• Patients unable to give informed consent Study Assessments and Data Collection

The study will include clinical, biological, and immunological assessments:

• DAS28-CRP scores at baseline, 6, and 12 months
• Immunological assays (B/T cell phenotyping, immunoglobulin levels, HACA)
• Vaccine serologies (Diphtheria, Pneumococcus, Tetanus, Haemophilus, SARS-CoV-2)
• Quality-of-life surveys (EQ-5D-5L, SF-36, RAPID-3)
• Adverse event monitoring

Sample Size Calculation:

The trial requires 260 patients to achieve 92% power to detect non-inferiority, using a linear mixed model with a non-inferiority margin of -0.3 on DAS28-CRP.

Expected Impact

If 200 mg of Rituximab proves non-inferior to 1g, this study could redefine maintenance therapy guidelines, reducing:

• Drug exposure and immune suppression risks
• Serious infections and adverse events
• Healthcare costs, improving access in resource-limited settings By providing definitive clinical and immunological data, the RADAR trial has the potential to influence global RA management and enhance long-term treatment safety.

Inclusion criteria

• Age ≥ 18 years
• Diagnosis of rheumatoid arthritis (RA) according to EULAR/ACR 2010 classification criteria
• DAS28 ≤ 5.1
• Current maintenance treatment with Rituximab regardless of dose and/or duration of Rituximab treatment and with at least first cycle of Rituximab ended (2 initial infusions)
• Last Rituximab infusion between 6 and 18 months prior to inclusion
• Corticosteroids ≤10 mg/day within 4 weeks prior to inclusion
• Affiliation to a social insurance system or beneficiary
• Written informed consent to participate in the study, dated and signed before starting the trial
• Effective method of birth control during the study

Exclusion criteria

• Rheumatic autoimmune disease other than RA (except associated Sjogren's disease, which is allowed)
• Concurrent treatment with any other targeted therapy than Rituximab
• Any contraindication to Rituximab or to NaCl 0.9%
• Significant uncontrolled associated disease or comorbidity
• Known active infection or history of serious recurrent or chronic infection
• Laboratory findings: active or untreated latent tuberculosis, hepatitis B positive, hepatitis C positive, haemoglobin <8 g/dL, neutropenia < 1.5G/L, IgM <0.4 g/L and/or IgG <5 g/L
• Pregnancy, breastfeeding, or planned pregnancy during the study (on subject declaration)
• Drug addiction, alcohol addiction
• Patients who cannot be followed for the 12 month-duration
• Patients over the age of legal majority who are protected, or deprived of liberty by judicial or administrative decision
• Subject in exclusion period (determined by a previous or ongoing study)
• Patients unable to give informed consent (e.g., patients in a situation of medical emergency, patients who have difficulty comprehending the essential details of the trial...)
• Patients who have difficulty reading or understanding French, or who have an inability to understand the delivered information