Ultrasound and Withdrawal of Biological DMARDs in Rheumatoid Arthritis

Phase 4TerminatedNCT01602302

Medical University of Graz40 enrolled

Overview

biological DMARDs may be stopped in Rheumatoid Arthritis (RA) patients treated with a combination of synthetic DMARD plus bDMARDs which are in persistent clinical remission. The research question of this study is, whether musculoskeletal sonography is a useful biomarker predicting a disease flare after cessation of bDMARD therapy.

Rheumatoid arthritis (RA) is the most common inflammatory joint disease. It is usually treated with synthetic and biologic disease modifying antirheumatic drugs (DMARDs). Up to 35% of patients can achieve clinical remission by the combination these therapies; however, there is considerable uncertainty regarding the management of patients once this clinical state is achieved. The discontinuation of biological agents in patients with persistent clinical remission may be beneficial for the patients and the health care system reducing the risks of long term adverse events and saving costs, respectively. Up to 60% of patients were reported to flare after cessation of anti-tumor necrosis factor alpha (TNF alpha) therapy despite continuation of synthetic DMARDs and up to now there exist no validated biomarkers that predict which patients will suffer a flare and which patients will remain in remission. Sonography is more and more used as a biomarker in RA. Subclinical inflammation was previously associated with an increased risk for short term clinical relapse and structural deterioration. The hypothesis of this prospective study is that ultrasound verified subclinical inflammation at the time of bDMARD withdrawal predicts a disease flare at week 16. The investigators plan to recruit RA-patients with persistent clinical remission according to SDAI and no current corticosteroid therapy. At baseline, bDMARD is stopped, synthetic DMARDs are continued. Patients undergo 9 study visits within 52 weeks. Ultrasound examinations of 14 joints as well as clinical and laboratory assessments with calculation of SDAI scores are performed at each visit. Patients are considered to have a disease flare if disease status changes from remission to active disease according to clinical scores. Patients with a flare of the disease are excluded from the active phase of the study and are treated according to current guidelines.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Rheumatoid Arthritis

Interventions

bDMARD withdrawal (etanercept, adalimumab, infliximab, certolizumab, golimumab, tozilizumab, abatacept)DRUG

bDMARDS (etanercept, adalimumab, infliximab, certolizumab, golimumab, tocilizumab, abatacept) will be discontinued after baseline visit in all participants

Eligibility

Sex: ALLMin age: 18 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female patient ≥18 years and \<90 years of age * Classification of RA according to the ACR/EULAR 2010 criteria * Persistent clinical remission as defined by the ACR/EULAR remission criteria for at least 6 months (documented at ≥2 visits) * Written informed consent * Current treatment with a single csDMARD or a combination of csDMARDs plus a stable dose and administration interval (for the last 6 months) of a TNF-alpha inhibitor * No current systemic corticosteroid treatment (stopped for at least 4 weeks), no corticosteroid injection within 4 weeks * Stable dose of NSAIDs for at least 1 week Exclusion Criteria: * • Current treatment with any investigational drug * Current administration interval of the anti-TNF-alpha agent of \>11 weeks * Complete destruction of any joint to be investigated by sonography * Current RA-related vasculitis or other active systemic (i.e. extraarticular) RA- manifestation with the exception of rheumatoid nodules * Initial arthritis manifestations before the age of 17 years * Planned surgery within the study period or history of surgery of any of the joints to be investigated clinically or by sonography * Current severe medical illness requiring hospitalization * Active infection or active malignancy at screening or infection during the past 4 weeks requiring (even temporary) discontinuation of the anti-TNF-alpha agent * Pregnancy or lactation * Inability of the patient to follow the protocol * Current treatment with Rituximab (MabThera®)

Locations (1)

Medical University Graz

Graz, Austria

Outcomes

Primary Outcomes

PD-signals predict relapse at week 16

Active inflammation at the time of bDMARD withdrawal indicated by the presence of a PD-score ≥1 in at least one joint out of a sonographic 14-joint count predicts relapse rate at week 16.

Time frame: 16 weeks

Secondary Outcomes

PD-signals predict relapse at week 24

Active inflammation at the time of bDMARD withdrawal indicated by the presence of a PD-score ≥1 in at least one joint out of a sonographic 14-joint count predicts relapse rate at week 24

Time frame: 24 weeks

PD-signals predict relapse at week 52

Active inflammation at the time of bDMARD withdrawal indicated by the presence of a PD-score ≥1 in at least one joint out of a sonographic 14-joint count predicts relapse rate at week 52

Time frame: 52 weeks

PD-scores at time of relapse

RA-patients have higher PD-scores at time of a clinical flare compared to patients with maintained clinical remission

Time frame: 24 weeks

Increment of PD-scores precede flare

An increment of PD-scores at follow-up compared to baseline visits precedes a clinical flare

Time frame: 52 weeks

PD scores better predict a relapse than residual swollen joints

PD scores better predict a relapse at week 16, 24 and 52 than the presence of residual swollen joints

Time frame: 16, 24, 52 weeks

PD score at baseline correlates with relapse risk

The higher the PD score at baseline, the more likely is a relapse at weeks 16, 24 and/or 52

Data from ClinicalTrials.gov

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