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PsoBest - the German Psoriasis Registry

U

Universitätsklinikum Hamburg-Eppendorf

Status

Enrolling

Conditions

Psoriasis
Psoriatic-arthritis

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01848028
IVDP-085-07

Details and patient eligibility

About

Treatment of moderate to severe Psoriasis (Pso) and Psoriasis-Arthritis (PsA) is largely confined to systemic therapy in Germany. Systemic therapy includes conventional systemic therapy (e.g. fumaric acids, methotrexate, ciclosporin A) and biological treatment (e.g. adalimumab, etanercept). While short- and middle-term efficacy of most systemic treatments has been shown in clinical studies (and is incorporated in international guidelines), knowledge about long-term outcomes, optimal treatment and effectiveness under real-world conditions is still missing. PsoBest, the German registry on the treatment of moderate to severe Pso and PsA started in 2008 and documents the long-term course of patients being administered any biologic or conventional systemic antipsoriatic drug authorized in Germany for the first time. The registry evaluates the long-term course of 3,500 patients with Pso and PsA treated with systemic antipsoriatics.

Full description

Background: Treatment of moderate to severe Psoriasis (Pso) and Psoriasis-Arthritis (PsA) is largely confined to systemic therapy in Germany. Systemic therapy includes conventional systemic therapy (e.g. fumaric acids, methotrexate, ciclosporin A) and biological treatment (e.g. adalimumab, etanercept). While short- and middle-term efficacy of most systemic treatments has been shown in clinical studies (and is incorporated in international guidelines), knowledge about long-term outcomes, optimal treatment and effectiveness under real-world conditions is still missing. PsoBest, the German registry on the treatment of moderate to severe Pso and PsA started in 2008 and documents the long-term course of patients being administered any biologic or conventional systemic antipsoriatic drug authorized in Germany for the first time.

Objectives: Observation and analysis of the following outcomes of treatment with systemic antipsoriatics:

  1. Effectiveness in clinical practice ("real world")
  2. Benefits and needs on the patients' side
  3. Effectiveness in a long-term course over years
  4. Optimal maintenance dosages
  5. Safety and side-effects profile under routine conditions
  6. Use in case of and effect on co-morbidity
  7. Reliable predictors of response
  8. Benefit and effectiveness of possible combination therapies or alternating use of biologics and systemic therapies

Methods: The registry evaluates the long-term course of 3,500 patients with Pso and PsA treated with systemic antipsoriatics.The registry started for seven treatment arms: Fumaric acid, methotrexate, ciclosporin A, efalizumab, etanercept, infliximab and adalimumab. While efalizumab was withdrawn from the market, ustekinumab was included after authorization. Patients are included at first initiation of a given treatment and will remain in the registry for 5 years, regardless of subsequent therapy. Nationwide, dermatologic practices and hospital ambulances with expertise in systemic and biologic treatment consecutively enrol patients. Follow-ups will be every 3 to 6 months, comprising patient and treatment characteristics, clinical parameters, patient-defined benefit, quality of life and adverse events. Standardized questionnaires will be addressed to the patient and to the dermatologist 12 times at the dermatologic centres. In interim intervals, patients are directly contacted another 9 times by mail. PsoBest is member of the ENCePP network of psoriasis-registries (www.psonet.eu).

Enrollment

3,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with diagnosis of plaque-type psoriasis or psoriasis arthritis confirmed by a dermatologist
  • age ≥ 18 years
  • being administered a specific systemic drug for the first time
  • informed consent to participate
  • sufficient language skills (German)

Exclusion criteria

  • lack of informed consent
  • patients being participants of clinical trials at the day of admission to the registry (if a patient is included into a clinical trial during the registry follow-ups, the patient data will be recorded, but analysed separately)

Trial design

3,500 participants in 25 patient groups

Fumaric acid esters
Description:
Intervention: Drug: conventional systemic: Fumaric acid esters, including Dimethylfumarate, all dosages, frequencies and durations prescribed
Methotrexate
Description:
Intervention: Drug: conventional systemic: Methotrexate, all dosages, frequencies and durations prescribed
Cyclosporine A
Description:
Intervention: Drug: conventional systemic: Cyclosporine A, all dosages, frequencies and durations prescribed
Efalizumab (withdrawn)
Description:
Intervention: Biological: Efalizumab, all dosages, frequencies and durations prescribed
Etanercept
Description:
Intervention: Biological and biosimilars: Etanercept, all dosages, frequencies and durations prescribed
Infliximab
Description:
Intervention: Biological and Biosimilars/-identicals: Infliximab, all dosages, frequencies and durations prescribed
Adalimumab
Description:
Intervention: Biological and Biosimilars: Adalimumab, all dosages, frequencies and durations prescribed
Ustekinumab
Description:
Intervention: Biological and Biosimilars: Ustekinumab, all dosages, frequencies and durations prescribed
Golimumab
Description:
Intervention: Biological: Golimumab, all dosages, frequencies and durations prescribed
Secukinumab
Description:
Intervention: Biological: Secukinumab, all dosages, frequencies and durations prescribed
Apremilast
Description:
Intervention: Small molecule: Apremilast, all dosages, frequencies and durations prescribed
Certolizumab
Description:
Intervention: Biological: Certolizumab, all dosages, frequencies and durations prescribed
Retinoids
Description:
Intervention: Drug: conventional systemic: Retinoids, all dosages, frequencies and durations prescribed
Leflunomids
Description:
Intervention: Drug: conventional systemic: Leflunomids, all dosages, frequencies and durations prescribed
systemic PUVA
Description:
Intervention: Drug: conventional systemic: systemic PUVA, all dosages, frequencies and durations prescribed
Guselkumab
Description:
Intervention: Biological: Guselkumab all dosages, frequencies and durations prescribed
Brodalumab
Description:
Intervention: Biological: Brodalumab, all dosages, frequencies and durations prescribed
Tildrakizumab
Description:
Intervention: Biological: Tildrakizumab, all dosages, frequencies and durations prescribed
Risankizumab
Description:
Intervention: Biological: systemic Risankizumab, all dosages, frequencies and durations prescribed
Bimekizumab
Description:
Intervention: Biological: Bimekizumab, all dosages, frequencies and durations prescribed
Tofacitinib
Description:
Intervention: JAK-Inhibitor: Tofacitinib, all dosages, frequencies and durations prescribed
Upadacitinib
Description:
Intervention: JAK-Inhibitor: Upadacitinib, all dosages, frequencies and durations prescribed
Deucravacitinib
Description:
Intervention: JAK-Inhibitor: Deucravacitinib, all dosages, frequencies and durations prescribed
Ixekizumab
Description:
Intervention: Biological: Ixekizumab, all dosages, frequencies and durations prescribed
No treatment
Description:
Intervention: no systemic treatment in observation episodes

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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