Study of the Response and Cardiorespiratory Endurance in Early RA Patients Treated With Tocilizumab or Methotrexate

Patrick Durez30 enrolled

Overview

To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone. The secondary endpoints : analyze the clinical efficacy of Tocilizumab in this population and correlate the CRE response with other marker (CRP, Hb, DAS, HAQ) and evaluate the safety profile of Tocilizumab.

Rheumatoid arthritis (RA) is the most prevalent (about 1%) inflammatory rheumatic disorder. Interleukin-6 (IL-6) has emerged as a potential therapeutic target in RA. This is based on the greater understanding of the role this cytokine can play in various aspects of the pathogenesis of RA. It has been shown that IL-6 is responsible for various clinical symptoms, including,fatigue, anemia, anorexia, fever, as well as the production of autoantibodies and increase in the erythrocyte sedimentation rate, all of which develop in patients with RA. Tocilizumab, as monotherapy and in combination with methotrexate, has been shown to be effective for RA patients with insufficient response to methotrexate or other disease-modifying antirheumatic drugs. These observations about the effects of tocilizumab were extended to patients refractory to tumor necrosis factor inhibitors. Tocilizumab also slows down the progression of structural joint damage. Furthermore, a 5-year long-term safety and efficacy has been shown. The place of Tocilizumab therapy in early RA is still unknown. Cardiorespiratory endurance (CRE), the most fundamental component of physical fitness can be severely impaired in patients with rheumatoid arthritis (RA). It has been shown that intensive and early treatment of RA can induce sustained clinical remission, improve general health and physical fitness and might therefore have an impact on the quality of life of RA patient. This study was planned to measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Rheumatoid Arthritis

Interventions

TocilizumabDRUG

Tocilizumab (8 mg/kg monthly from week 0 to 20)

MethotrexateDRUG

MTX at a dose ranging from 10 mg/week at baseline to 20 mg/week at week 8

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosis of RA (according to American College of Rheumatology ACR criteria) * Disease duration \< 2 years. * Age between 18 and 70 years old. * Active RA defined by a disease activity score 28 DAS28-CRP score \> 3.2 with a swollen joint count ≥ 4 * MTX naive * Stable therapy with corticosteroids or nonsteroidal anti-inflammatory drug NSAIDs * Presence of knee arthralgia or synovitis (addendum protocol with synovial biopsy). Exclusion Criteria: Previous MTX treatment. Exclusion for severe physical handicap to perform CRE. Exclusion for general safety (history of severe allergic reaction, sepsis, malignancy within 5 years, pregnancy, severe heart failure) Concurrent treatment with other DMARDs than MTX or any anti-TNF and biological therapies.

Locations (1)

Université Catholique de Louvain

Brussels, Belgium

Outcomes

Primary Outcomes

To measure the CRE by a work capacity index obtained in a submaximal testing (W65%/kg) in early RA patients treated with tocilizumab compared to Methotrexate alone.

not necessary

Time frame: 2 years

Secondary Outcomes

To analyze the clinical efficacy of Tocilizumab in this population.

no necessary

Time frame: 2 years

To correlate the CRE response with other marker (CRP, Hb, Disease activity score DAS, HAQ).

no necessary

Time frame: 2 years

To evaluate the safety profile of Tocilizumab.

no necessary

Time frame: 2 years

To assess the effect of Tocilizumab on synovial histopathology of early RA

not necessary

Time frame: 2 years

Data from ClinicalTrials.gov

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