BIOTAPE: Biologic Tapering Study of TNF Inhibitors in Axial Spondyloarthritis

Sponsor

University Health Network, Toronto (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT05115903

Collaborator

(none)

156

Enrollment

Arms

12.9

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Current evidence on tapering of tumor necrosis factor inhibitors (TNFi) in axial spondyloarthritis (axSpA) is still hampered by heterogeneity in tapering regimens, selection and performance biases, and lack of data on optimized treatment dosing strategies especially in real-world clinical settings. This study aims to contribute to the ongoing investigation of disease-activity-guided tapering of TNFi in axSpA in the form of a prospective, randomized controlled trial.

Condition or Disease	Intervention/Treatment	Phase
Axial Spondyloarthritis	Drug: Tapered doses of TNFi Drug: Standard dose of TNFi	Phase 4

Detailed Description

This is a 48-week randomized, controlled, open-label, non-inferiority trial of patients with radiographic or non-radiographic axial spondyloarthritis. The study will include 156 patients with inactive disease or low disease activity (LDA) for at least 6 months on a TNFi at the time of randomization.

Participants will be randomized using a 1:1 ratio to either the tapered-dose arm or the standard-dose arm of TNFi. Progressive tapering of TNFi according to a predefined protocol will be allowed as long as the patient is able to maintain inactive disease or LDA during the study period. We hypothesize that, in patients with 6 months or more of inactive or low-activity axial spondyloarthritis, tapered-dose TNFi are non-inferior to standard-dose TNFi in sustaining the disease state for at least 1 year.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

156 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Prospective, Randomized Biologic Tapering Study of TNF Inhibitors in Axial Spondyloarthritis

Anticipated Study Start Date :

Nov 1, 2021

Anticipated Primary Completion Date :

Nov 30, 2022

Anticipated Study Completion Date :

Nov 30, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Tapered doses of TNFi Tapering of TNFi through standardized increases in the dosing interval between drug administration. The tapering dose intervals for each TNFi are designed to decrease the dose from baseline by 75% for 12 weeks, 50% for 24 weeks, and 25% for 12 weeks	Drug: Tapered doses of TNFi To be given subcutaneously via a prefilled syringe/autoinjector (etanercept, adalimumab, certolizumab pegol, golimumab) or intravenously via infusion (infliximab) at increasing dose intervals as specified Other Names: etanercept 50 mg every 10 days (75% of baseline dose), 14 days (50%), 30 days (25%) adalimumab 40 mg every 3 weeks (75%), 4 weeks (50%), 16 weeks (25%) certolizumab pegol 200 mg 3 weeks (75%), 4 weeks (50%), 16 weeks (25%) golimumab 50 mg every 6 weeks (75%), 8 weeks (50%), 16 weeks (25%) infliximab 5 mg/kg every 8 weeks (75%), 12 weeks (50%), 16 weeks (25%)
Active Comparator: Standard dose of TNFi Stable doses of TNFi according to the approved summary of product characteristics for biologic agents used in axial spondyloarthritis	Drug: Standard dose of TNFi To be given subcutaneously via a prefilled syringe/autoinjector (etanercept, adalimumab, certolizumab pegol, golimumab) or intravenously via infusion (infliximab) Other Names: etanercept 50 mg every 7 days adalimumab 40 mg every 2 weeks certolizumab pegol 200 mg every 2 weeks golimumab 50 mg every 4 weeks infliximab 5 mg/kg every 6 weeks

Arm

Intervention/Treatment

Experimental: Tapered doses of TNFi

Tapering of TNFi through standardized increases in the dosing interval between drug administration. The tapering dose intervals for each TNFi are designed to decrease the dose from baseline by 75% for 12 weeks, 50% for 24 weeks, and 25% for 12 weeks

Drug: Tapered doses of TNFi

To be given subcutaneously via a prefilled syringe/autoinjector (etanercept, adalimumab, certolizumab pegol, golimumab) or intravenously via infusion (infliximab) at increasing dose intervals as specified

Other Names:

etanercept 50 mg every 10 days (75% of baseline dose), 14 days (50%), 30 days (25%)

adalimumab 40 mg every 3 weeks (75%), 4 weeks (50%), 16 weeks (25%)

certolizumab pegol 200 mg 3 weeks (75%), 4 weeks (50%), 16 weeks (25%)

golimumab 50 mg every 6 weeks (75%), 8 weeks (50%), 16 weeks (25%)

infliximab 5 mg/kg every 8 weeks (75%), 12 weeks (50%), 16 weeks (25%)

Active Comparator: Standard dose of TNFi

Stable doses of TNFi according to the approved summary of product characteristics for biologic agents used in axial spondyloarthritis

Drug: Standard dose of TNFi

To be given subcutaneously via a prefilled syringe/autoinjector (etanercept, adalimumab, certolizumab pegol, golimumab) or intravenously via infusion (infliximab)

Other Names:

etanercept 50 mg every 7 days

adalimumab 40 mg every 2 weeks

certolizumab pegol 200 mg every 2 weeks

golimumab 50 mg every 4 weeks

infliximab 5 mg/kg every 6 weeks

Outcome Measures

Primary Outcome Measures

Proportion of patients able to maintain inactive disease or low disease activity, defined as Ankylosing Spondylitis Disease Activity Score (ASDAS) <1.3 to 2.1 or Bath Ankylosing Spondylitis Disease Activity Score (BASDAI) of <4 on tapered-dose TNFi [Weeks 12, 24, 36, and 48]
The ASDAS and BASDAI are measures of axial spondyloarthritis disease activity for the past week. The ASDAS has 5 components scored from 0 to 10 (none to very severe). The following formula is used to compute for the ASDAS: (0.121 × back pain score) +(0.058 × score for duration of morning stiffness) + (0.11 × patient global assessment score) + (0.073 × peripheral pain/swelling score) + (0.579 × log(CRP+1)). The disease is considered inactive if the final score is <1.3, and low if <2.1. The BASDAI consists of six items, with each item being scored from 0 ("none") to 10 ("very severe"). The final BASDAI scores ranges from 0 to 10, with lower scores indicating lower disease activity. A BASDAI of <4 indicates inactive or low disease. As opposed to ASDAS, BASDAI does not include CRP in its formula. Either ASDAS or BASDAI is acceptable in clinical practice.

Secondary Outcome Measures

Proportion of patients experiencing a disease flare by ASDAS or BASDAI [Up to Week 48]
Flare is defined in this study as either of the following: loss of inactive disease or LDA (ASDAS ≥2.1 or BASDAI ≥4) - see definitions above minimal clinically important worsening, defined as an increase in ASDAS by ≥0.9
Proportion of patients with functional limitation measured using the Bath Ankylosing Spondylitis Functional Index (BASFI) [Up to Week 48]
The BASFI measures the degree of functional limitation. It is composed of a set of 10 questions relating to activities during the past week. Each item is scored from 0 ("easy") to 10 ("impossible"). The final BASFI is the mean of the 10 scores with the total score ranging from 0 to 10. Lower scores indicate better physical function.
Mean quality of life in the tapered-dose arm vs. the standard-dose arm measured using the Ankylosing Spondylitis Quality of Life (ASQoL) questionnaire [Up to Week 48]
The ASQoL measures health-related quality of life (HRQoL) in subjects with axial spondyloarthritis. The final ASQoL score ranges from 0 to 18, with higher scores indicating worse HRQoL.
Proportion of patients with impaired work productivity and activity measured using the Work Productivity and Activity Impairment Questionnaire for Ankylosing Spondylitis (WPAI:SpA) questionnaire [Up to Week 48]
The WPAI:SpA consists of 6 questions to determine employment status, hours missed from work because of SpA, hours missed from work for other reasons, hours actually worked, the effect of SpA on work productivity while at work, and the effect of SpA on activities outside of work. The 4 scores derived include percentage of absenteeism, percentage of presenteeism (reduced productivity while at work), an overall work impairment combining absenteeism and presenteeism, and percentage of impairment in activities performed outside of work. The computed percentage for each sub-scale ranges from 0 to 100. Higher scores indicate greater impairment and less productivity.
Proportion of patients with radiographic progression, defined as an increase in the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) by 2 units [Baseline and Week 48]
The mSASSS measures the sum of the lumbar and cervical spine score from 0 (no change) to 72 (progression). The score is derived from grading of the anterior aspect of the vertebral bodies of the lumbar spine (T12 to S1) and the cervical spine (C2 to T1). Grading is as follows: 0 (normal), 1 (erosion, sclerosis, or squaring), 2 (syndesmophyte), 3 (bridging syndesmophyte), or N (vertebral body not evaluable).
Proportion of patients needing concomitant medication [Up to Week 48]
Concomitant medications will include NSAIDs, conventional synthetic DMARDs, and/or targeted synthetic DMARDs used during the study period
Proportion of patients with any related severe adverse event [Up to Week 48]
Severe adverse event, defined as serious infections requiring systemic antibiotic use and/or hospitalization assessed to be at least possibly related to TNFi use or withdrawal
Factors predicting flare [Up to Week 48]
Factors including but not be limited to the following: sex, human leukocyte antigen (HLA)-B27 status, disease duration, duration of remission, ASDAS at the start of taper, and MRI findings at the time of taper

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Adult axSpA patients satisfying the 2009 Assessment of SpondyloArthritis International Society (ASAS) Classification Criteria
Currently enrolled in the SPARCC Program with successful completion of standard data collection protocol in the Spondylitis Clinic of UHN-Toronto Western Hospital
Have sustained inactive disease or LDA with an ASDAS of <2.1 or BASDAI <4 for at least 6 months
On a stable dose of a TNFi (infliximab, etanercept, adalimumab, certolizumab pegol, or golimumab)

Exclusion Criteria:

Adults axSpA patients with active extra-articular manifestations such as inflammatory bowel disease, psoriasis, and/or uveitis
Have comorbidities that may preclude clinical assessment (i.e. fibromyalgia or other chronic pain syndromes; chronic inflammatory diseases other than axSpA)
Have diagnosed psychiatric or personality disorders
Not enrolled in the Spondyloarthritis Research Consortium of Canada (SPARCC) Program