Evidence map›Paper›PMID 32378070›Full record

ArticleAdvances in therapy2020

Secukinumab Use in Patients with Moderate to Severe Psoriasis, Psoriatic Arthritis and Ankylosing Spondylitis in Real-World Setting in Europe: Baseline Data from SERENA Study.

Uta Kiltz, Petros P Sfikakis, Karl Gaffney, Paul-Gunther Sator, Ralph von Kiedrowski, Andreas Bounas, Nicola Gullick, Curdin Conrad, Dimitris Rigopoulos, Eric Lespessailles and 12 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06905288 (Real-world Observational Study to Evaluate the Effectiveness of Secukinumab in Biologic-naive Ankylosing Spondylitis Patients in Korea), which is not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06905288 recruitingnot on this mapstarted 2025, after this paper: background citation

Real-world Observational Study to Evaluate the Effectiveness of Secukinumab in Biologic-naive Ankylosing Spondylitis Patients in Korea

TypeobservationalSponsorNovartis PharmaceuticalsRan2025 to 2026Enrolled70ConditionsAnkylosing SpondylitisArmsSecukinumab
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Secukinumab in axial spondyloarthritis: a narrative review of clinical evidence.Therapeutic advances in musculoskeletal disease · 2021
    Review
  15. Article
  16. Review
  17. Cutaneous Vasculitis During Secukinumab Treatment.European journal of case reports in internal medicine · 2020
    Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 14 institutions in 9 countries.

Uta KiltzRheumazentrum Ruhrgebiet, Herne, Germany. Uta.Kiltz@elisabethgruppe.de.
Petros P SfikakisJoint Rheumatology Programme, National and Kapodistrian University of Athens Medical School, Athens, Greece.
Karl GaffneyNorfolk and Norwich University Hospital NHS Foundation Trust, Norfolk, UK.
Paul-Gunther SatorDepartment of Dermatology, Municipal Hospital Hietzing, Vienna, Austria.
Ralph von KiedrowskiCompany for Medical Study & Service Selters (CMS3) GmbH, Selters, Germany.
Andreas BounasOlympion Therapeutirion, Patras, Greece.
Nicola GullickUniversity Hospitals Coventry & Warwickshire NHS Trust, Coventry, UK.
Curdin ConradCentre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Dimitris RigopoulosDermatology and Venerology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Eric LespessaillesRegional Hospital and University of Orleans, Orleans, France.
Marco RomanelliDermatology Department, University of Pisa, Lungarno Antonio Pacinotti, 43, 56126, Pisa, PI, Italy.
Pierre-Dominique GhislainDermatology, Cliniques Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
Jan Brandt-JürgensRheumatologische Schwerpunktpraxis, Berlin, Germany.
Rasho RashkovDepartment of Internal Medicine, Medical University, Sofia, Bulgaria.
Maher AassiNovartis Pharma AG, Basel, Switzerland.
Roberto OrsenigoNovartis Farma SpA, Origgio, Italy.
Chiara PerellaNovartis Pharma AG, Basel, Switzerland.
Effie PournaraNovartis Pharma AG, Basel, Switzerland.
Sven GathmannNovartis Pharma AG, Basel, Switzerland.
Piotr JagielloNovartis Pharma AG, Basel, Switzerland.
Justyna VeitNovartis Pharma GmbH, Nuremberg, Germany.
Matthias AugustinInstitute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg, Hamburg, Germany.
Novartis (Switzerland) · CHNational and Kapodistrian University of Athens · GRCentre hospitalier régional d'Orléans · FRKlinik Hietzing · ATMedical University of Sofia · BGNorfolk and Norwich University Hospitals NHS Foundation Trust · GBNovartis (Germany) · DENovartis (Italy) · ITRheumazentrum Ruhrgebiet · DEUCLouvain · BEUniversität Hamburg · DEUniversity Hospital of Lausanne · CHUniversity Hospitals Coventry and Warwickshire NHS Trust · GBUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSecukinumab, a fully human monoclonal antibody that directly inhibits interleukin-17A, has demonstrated robust efficacy in the treatment of moderate to severe psoriasis (PsO), psoriatic arthritis (PsA) and ankylosing spondylitis (AS), with a rapid onset of action, sustained long-term clinical responses and a consistently favourable safety profile across phase 3 trials. Here, we report the clinical data at enrolment from SERENA, designed to investigate the real-world use of secukinumab across all three indications.

methodsSERENA is an ongoing, longitudinal, observational study conducted at 438 sites across Europe in patients with moderate to severe plaque PsO, active PsA or active AS. Patients should have received at least 16 weeks of secukinumab treatment before enrolment in the study.

resultsOverall 2800 patients were included in the safety set; patients with PsA (N = 541) were older than patients with PsO (N = 1799) and patients with AS (N = 460); patients with PsO had a higher mean body weight than patients with PsA and patients with AS; and patients with PsO and patients with AS were predominantly male. Time since diagnosis was longer in patients with PsO compared with patients with PsA and patients with AS, and about 40% of patients were either current or former smokers. The proportion of obese patients (body mass index ≥ 30 kg/m

conclusionBaseline demographics of the study population are consistent with existing literature. This large observational study across all secukinumab indications will provide valuable information on the long-term effectiveness and safety of secukinumab in the real-world setting.

Indexed as

AdultAntibodies, Monoclonal, HumanizedArthritis, PsoriaticEuropeFemaleHumansLongitudinal StudiesMaleMiddle AgedPsoriasisSpondylitis, AnkylosingAntibodies, Monoclonal, HumanizedAnkylosing spondylitisBiologicsObservationalPsoriasisPsoriatic arthritisReal-worldRheumatologySafetySecukinumab

Identifiers

PMID32378070
PMCPMC7467439
OpenAlexW3022081125

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.