Psoriatic Oligoarthritis Intervention With Symptomatic thErapy

Overview

POISE is a two arm interventional trial nested within a cohort (Trials Within Cohorts or TWiCs design). This tests less aggressive early therapy in patients newly diagnosed with low impact oligoarticular PsA. Arm 1 will receive standard step up therapy in the cohort and act as the control group. Arm 2 will receive local steroid injections to active joints and will be able to use non-steroidal anti-inflammatory drugs (NSAIDs) only

Full Title of Study: “Clinical Effectiveness of Symptomatic Therapy Compared to Standard Step up Care for the Treatment of Low Impact Psoriatic Oligoarthritis: a 2 Arm Parallel Group Feasibility Study”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: September 2021

Detailed Description

Arm 1: Control 'step-up' therapy in the cohort (MONITOR-PsA study). Therapy for the cohort is defined by standard practice in these PsA clinics following current international recommendations and National requirements for the prescription of biologic therapy. Whilst physician discretion is used, most commonly Initial therapy will be with methotrexate alone (15mg/week rising to 25mg/week as tolerated by week 8 of therapy) unless this is contraindicated. In cases of non-response or intolerance to methotrexate, participants will have an alternative DMARD (most commonly sulfasalazine or leflunomide) added or switched to at the discretion of the rheumatologist. In cases of failure of two DMARDs, treatment can be escalated to biologic therapy as per National Institute for Health and Clinical Excellence (NICE) recommendations usually with a TNF inhibitor as first line. If the requisite disease activity is not met or if there are contraindications to biologics, alternative DMARD combinations will be used. Further details are available in the PsA clinic treatment protocol which is Appendix D in the MONITOR-PsA protocol.

Arm 2: Symptomatic therapy arm. The intervention will delay standard treatment with disease-modifying anti-rheumatic drugs (DMARDs) and use local glucocorticoid injections to affected joints instead. Oral non-steroidal anti-inflammatory drugs (NSAIDs) will also be allowed as concomitant medication as indicated for individuals. Local glucocorticoid injections will include injections with methylprednisolone or triamcinolone. All active joints will be treated with glucocorticoid injections. Glucocorticoid injections can be either be given as an intra-articular injection to an inflamed joint or as an intra-muscular injection if multiple joints are involved. If any joint requires more than 2 local injections of glucocorticoid within a 6 month period, then the patient is deemed to have failed symptomatic therapy and will be withdrawn from the treatment protocol and be treated as per usual care (in most cases with DMARD therapy). If Participants require DMARD therapy, they will be offered rescue therapy as per usual clinical care but will be asked to continue with data collection for the trial. This is to ensure that sufficient data is collected for the trial but risks in delaying treatment to the individual are mitigated.

Interventions

  • Drug: Methotrexate
    • Methotrexate up to 25mg/week as tolerated po or sc
  • Drug: Sulfasalazine
    • Sulfasalazine up to 3g daily po
  • Drug: Leflunomide
    • Leflunomide 10-20mg daily po
  • Drug: Methylprednisolone
    • For IA or IM injection 20-120mg
  • Drug: Triamcinolone
    • For IA or IM injection 20-120mg

Arms, Groups and Cohorts

  • Active Comparator: Standard care
    • Control ‘step-up’ therapy in the cohort (MONITOR-PsA study). Therapy for the cohort is defined by standard NHS practice. Commonly Initial therapy will be with methotrexate alone unless this is contraindicated. In cases of non-response or intolerance to methotrexate, participants will have an alternative DMARD (sulfasalazine or leflunomide). In cases of failure of two DMARDs, treatment can be escalated to biologic therapy as per National Institute for Health and Clinical Excellence (NICE) recommendations. If the requisite disease activity is not met or if there are contraindications to biologics, alternative DMARD combinations will be used.
  • Experimental: Local/IM steroid injections
    • Symptomatic therapy arm. The intervention will delay standard treatment with disease-modifying anti-rheumatic drugs (DMARDs) and use local injections of methylprednisolone or triamcinolone to affected joints instead. Oral non-steroidal anti-inflammatory drugs (NSAIDs) will also be allowed as concomitant medication. All active joints will be treated with injections. Injections can be either be given as an intra-articular injection or as an intra-muscular injection. If any joint requires more than 2 local injections of glucocorticoid within a 6 month period, then the patient is deemed to have failed symptomatic therapy and will be withdrawn from the treatment protocol and be treated as per usual care (in most cases with DMARD therapy).

Clinical Trial Outcome Measures

Primary Measures

  • To establish the feasibility of a future clinical trial
    • Time Frame: 48 weeks
    • To establish acceptability of this treatment approach assessing proportion of patients who are eligible, consent and complete the 48 week study.

Secondary Measures

  • Psoriatic arthritis disease activity score (PASDAS)
    • Time Frame: 48 weeks
    • A composite measure of PsA disease activity. This score is a composite measure of disease activity in PsA. There is only one total score which ranges from 0-10 with higher numbers indicating more active disease. Low disease activity is defined as <3.2.
  • Ultrasound score of synovitis
    • Time Frame: 0 weeks
    • A summary score of synovitis measured at baseline. The score will comprise of 23 joints bilaterally. Grey scale synovitis is scored at each site 0-3 and power doppler is also scored 0-3 at each site where higher scores indicate more severe disease. These scores are then summed to give a final score. Score range is 0-276
  • Ultrasound score of enthesitis
    • Time Frame: 0 weeks
    • A summary score of enthesitis measured at baseline. The score will comprise of 5 entheses bilaterally. Power doppler is scored 0-3 at each site where higher scores indicate more severe disease activity. Calcifications, enthesophytes and grey scale abnormalities will each be score 0 (absent) or 1 (present) at each site. These scores are then summed to give a final score. Score range is 0-30

Participating in This Clinical Trial

Inclusion Criteria

  • Participants consented to the PsA inception cohort (MONITOR-PsA) and to be approached for alternate interventional therapies.
  • Participants with mild disease as defined by:
  • Oligoarticular disease with <5 active joints at baseline assessment.
  • Low disease activity as defined by a PsA disease activity score (PASDAS) ≤3.2.
  • Low impact of disease as defined a PsA impact of disease (PSAID) ≤4.
  • Participant is willing and able to give informed consent for participation in the trial.
  • Male or female.
  • Aged 18 years or above.
  • Female Participants of child bearing potential and male Participants whose partner is of child bearing potential must be willing to ensure that they or their partner use effective contraception (defined as true abstinence, oral contraceptives, implants, intrauterine device, barrier method with spermicide, or surgical sterilization) during the trial and for 3 months thereafter if receiving DMARD therapy (excluding sulfasalazine).
  • Participant has clinically acceptable laboratory results within 6 weeks of enrolment:
  • Haemoglobin count > 8.5 g/dL
  • White blood count (WBC) > 3.5 x 109/L
  • Absolute neutrophil count (ANC) > 1.5 x 109/L
  • Platelet count > 100 x 109/L
  • ALT and alkaline phosphatase levels <3 x upper limit of normal
  • In the Investigator's opinion, is able and willing to comply with all trial requirements.
  • Willing to allow his or her GP and consultant, if appropriate, to be notified of participation in the trial.

Exclusion Criteria

  • ≥1 poor prognostic factors for psoriatic arthritis, from
  • raised C reactive protein (CRP) defined as > 4g/dl for standard non-hsCRP
  • radiographic damage defined as the presence of ≥ 1 erosion on plain radiographs of the hands and feet
  • health assessment questionnaire (HAQ) score > 1
  • Contraindications to non-steroidal anti-inflammatory drugs
  • Previous treatment for articular disease with synthetic DMARDs (including methotrexate, leflunomide or sulfasalazine) or biologic DMARDs (including TNF, IL12/23 or IL17 inhibitor therapies) or targeted synthetic DMARDs (PDE4 of JAK inhibitor therapies).
  • Female patient who is pregnant, breast feeding or planning pregnancy during the course of the trial.
  • Significant renal or hepatic impairment.
  • Scheduled elective surgery or other procedures requiring general anaesthesia during the trial.
  • Any other significant disease or disorder which, in the opinion of the Investigator, may either put the patients at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
  • Patients who have participated in another research trial involving an investigational product in the past 12 weeks.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • University of Oxford
  • Collaborator
    • National Institute for Health Research, United Kingdom
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Contact(s)
    • Laura C Coates, MBChB, PhD, +447870257823, laura.coates@ndorms.ox.ac.uk

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