The objective of the study is to evaluate two therapeutic strategies: "early switch" or "therapeutic intensification" in patients with spondyloarthritis in case of secondary treatment failure suspicion to a first monoclonal antibodies anti-TNF definite by increase of ASDAS and positivity to ADAb. Patients and Methods: Multicentric randomized prospective study. Duration of inclusion 30 months. Duration of follow-up 24 months. 104 patients with spondyloarthritis treated with infliximab or adalimumab will be included if their ADAb dosage is positive, and they will be randomized (1:1) in two groups : "early switch" where treatment will be change to another anti-TNF, or "therapeutic intensification" where interval between two injections will be shortened. Patients will be evaluated clinically (ASDAS) and biologically (ADAb) at 12 weeks then at 24 weeks. Principal outcome will be the variation of ASDAS between baseline and end of the study. Number of patients to be included has been determined statistically from a preliminary study (power \>98% for ASDAS variation of 20% on week 24). Expected results: On week 24, we expect a better response and a greater proportion of patients in remission in the "early switch" arm compare to the "therapeutic intensification" arm.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
8
anti drug antibodies dosage
UH Amiens
Amiens, France
UH Caen
Caen, France
Dieppe Hospital
Dieppe, France
Elbeuf Hospital
Elbeuf, France
UH Lille
Lille, France
Le Havre Hospital
Montivilliers, France
UH Rouen
Rouen, France
Variation of ASDAS between inclusion and 24 weeks of treatment
ASDAS will be measured at week 24 and will be compared to day 1
Time frame: Week 24
Frequency of patients with ASDAS < 2.1
Frequency of patients with ASDAS \< 2.1 at week 24 ASDAS \< 2.1 is considered as remission
Time frame: Week 24
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