Efficacy Comparison of Cycling Versus Transitioning to IL-17 Inhibitors Following Initial TNF Inhibitor Failure in Psoriatic Arthritis: A Multicenter Real-World Analysis - Scorecard - MDSpire

Efficacy Comparison of Cycling Versus Transitioning to IL-17 Inhibitors Following Initial TNF Inhibitor Failure in Psoriatic Arthritis: A Multicenter Real-World Analysis

  • By

  • Alarico Ariani

  • Maddalena Larosa

  • Alberto Lo Gullo

  • Olga Addimanda

  • Romina Andracco

  • Patrizia Del Medico

  • Marino Paroli

  • Maria Chiara Ditto

  • Bernd Raffeiner

  • Aurora Ianniello

  • Francesca Ometto

  • Marta Priora

  • Aldo Biagio Molica Colella

  • Elena Bravi

  • Viviana Ravagnani

  • Alessandra Bezzi

  • Rosetta Vitetta

  • Palma Scolieri

  • Alessandro Volpe

  • Federica Lumetti

  • Antonella Farina

  • Francesco Girelli

  • Elisa Visalli

  • Francesca Serale

  • Eleonora Celletti

  • Veronica Franchina

  • Francesco Molica Colella

  • Giulio Ferrero

  • Fabio Mascella

  • Maria Cristina Focherini

  • Alessia Fiorenza

  • Guido Rovera

  • Cecilia Giampietro

  • Simone Bernardi

  • Natalia Mansueto

  • Dario Camellino

  • Rosalba Caccavale

  • Valeria Nucera

  • Myriam Di Penta

  • Emanuela Sabatini

  • Ilaria Platè

  • Adorni Giuditta

  • Eleonora Di Donato

  • Daniele Santilli

  • Gianluca Lucchini

  • Mirco Magnani

  • Gianluca Smerilli

  • Giorgio Amato

  • Francesco De Lucia

  • Ylenia Dal Bosco

  • Roberta Foti

  • Francesco Cipollone

  • Gerolamo Bianchi

  • Rosario Foti

  • Eugenio Arrigoni

  • Antonio Marchetta

  • Vincenzo Bruzzese

  • Gilda Sandri

  • Enrico Fusaro

  • Massimo Reta

  • Dilia Giuggioli

  • Antonio Marchesoni

  • Simone Parisi

  • Andrea Becciolini

  • November 24, 2025

  • 0 min

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Clinical Scorecard: Efficacy Comparison of Cycling Versus Transitioning to IL-17 Inhibitors Following Initial TNF Inhibitor Failure in Psoriatic Arthritis: A Multicenter Real-World Analysis

At a Glance

CategoryDetail
ConditionPsoriatic Arthritis (PsA)
Key MechanismsTNF inhibitors (TNFi) and interleukin-17 inhibitors (IL-17i) as biological DMARDs with different mechanisms of action
Target PopulationPsA patients who failed first-line TNFi treatment
Care SettingRheumatology referral centers in Italy

Key Highlights

  • TNFi are first-line bDMARDs after csDMARD failure; IL-17i introduced as alternative MoA since 2016.
  • Study compares treatment retention (proxy for effectiveness) between cycling TNFi and swapping to IL-17i after first TNFi failure.
  • 452 PsA patients analyzed retrospectively from 25 centers; median follow-up 13 months; no baseline differences except HLA-B27 testing frequency.

Guideline-Based Recommendations

Diagnosis

  • PsA diagnosis according to CASPAR criteria.

Management

  • After csDMARD failure, initiate TNFi as first-line bDMARD.
  • Consider switching to IL-17i or cycling TNFi after first TNFi failure.
  • Exclude treatment changes for non-joint related reasons.

Monitoring & Follow-up

  • Assess disease activity using DAPSA for peripheral PsA and ASDAS/BASDAI for axial involvement.
  • Monitor treatment retention as a proxy for effectiveness.
  • Track reasons for treatment discontinuation including efficacy loss and adverse events.

Risks

  • Potential reduced effectiveness with repeated cycling of TNFi after multiple failures.
  • Adverse events leading to treatment discontinuation.

Patient & Prescribing Data

PsA patients who failed first-line TNFi and switched to either another TNFi or IL-17i.

Retention rate used as effectiveness proxy; switching to IL-17i may offer better retention than cycling TNFi based on prior studies.

Clinical Best Practices

  • Use standardized criteria (CASPAR) for PsA diagnosis before initiating bDMARDs.
  • Evaluate disease phenotype (peripheral, axial, mixed) and baseline activity to guide treatment choice.
  • Prefer switching to a different MoA (IL-17i) after first TNFi failure to potentially improve treatment retention.
  • Exclude patients switching bDMARDs for non-articular indications to focus on joint disease management.
  • Collect comprehensive baseline data including HLA-B27 status to inform prognosis.

References

Original Source(s)

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