Evidence map›Paper›PMID 33958325›Full record

Trial reportAnnals of the rheumatic diseases2021

Efficacy of a tight-control and treat-to-target strategy in axial spondyloarthritis: results of the open-label, pragmatic, cluster-randomised TICOSPA trial.

Anna Molto, Clementina López-Medina, Filip E Van den Bosch, Annelies Boonen, Casper Webers, Emanuelle Dernis, Floris A van Gaalen, Martin Soubrier, Pascal Claudepierre, Athan Baillet and 13 more

Registry-linked trialAbstract readPragmatic Clinical TrialRandomized Controlled Trial
In one paragraph

Trial report in Annals of the rheumatic diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03043846 (Treat to Target Trial in Axial Spondylo Arthritis), which is not on this map. Cited by 51 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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.

NCT03043846 completednot on this map

Treat to Target Trial in Axial Spondylo Arthritis : The TICOSPA (Tight Control in Spondyloarthritis)

TypeobservationalSponsorAssociation de Recherche Clinique en RhumatologieRan2016 to 2019Enrolled163ConditionsAxial SpondyloarthritisArmsFollow-up every 3 months during 1 year (data collection in eCRF), Follow-up every month to follow the pre-defined strategy
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Anna MoltoRheumatology Department, Hospital Cochin, Paris, France anna.molto@aphp.fr.ORCID 0000-0003-2246-1986
Clementina López-MedinaECAMO team, INSERM U1153, Paris, France.ORCID 0000-0002-2309-5837
Filip E Van den BoschRheumatology Department, University Hospital Ghent, Gent, Oost-Vlaanderen, Belgium.ORCID 0000-0002-3561-5932
Annelies BoonenDepartment of Internal Medicine, Division of Rheumatology, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0003-0682-9533
Casper WebersDepartment of Internal Medicine, Division of Rheumatology, Maastricht University, Maastricht, The Netherlands.
Emanuelle DernisRheumatology Department, Le Mans Hospital, Le Mans, France.
Floris A van GaalenRheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Martin SoubrierRheumatology, CHU, Clermont-Ferrand, France.
Pascal ClaudepierreRheumatology, Henri Mondor Hospital Rheumatology Service, Creteil, France.
Athan BailletRheumatology, Hopital Sud, Echirolles, France.ORCID 0000-0001-6006-2519
Mirian Starmans-KoolRheumatology, Zuyderland Medical Centre Heerlen, Heerlen, The Netherlands.
Anneke SpoorenbergRheumatology & Clinical Immunology, University Medical Centre Groningen, Groningen, The Netherlands.
Peggy JacquesRheumatology Department, University Hospital Ghent, Gent, Oost-Vlaanderen, Belgium.ORCID 0000-0001-9227-257X
Philippe CarronRheumatology, VIB-UGent Center for Inflammation Research, Zwijnaarde, Belgium.ORCID 0000-0001-9254-6171
Rik JoosRheumatology, ZNA UKJA, Antwerpen, Belgium.
Jan LenaertsRheumatology, Reumainstituut Hasselt, Hasselt, Belgium.
Laure GossecRheumatology Department, University Hospital Pitié Salpêtrière, Paris, France.ORCID 0000-0002-4528-310X
Sophie PouplinRheumatology, Bois-Guillaume CHU, Rouen, France.
Adeline Ruyssen-WitrandRheumatology, University Hospital Centre Toulouse, Toulouse, France.
Laetitia SparsaRheumatology department, Hospital Centre Mulhouse, Mulhouse, France.
Astrid van TubergenDepartment of Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0001-8477-0683
Désirée van der HeijdeDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-5781-158X
Maxime DougadosRheumatology Department, Hospital Cochin, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare the benefits of a tight-control/treat-to-target strategy (TC/T2T) in axial spondyloarthritis (axSpA) with those of usual care (UC).

methodsPragmatic, prospective, cluster-randomised, controlled, open, 1-year trial (NCT03043846). 18 centres were randomised (1:1). Patients met Axial Spondylo Arthritis International Society (ASAS) criteria for axSpA, had an Ankylosing Spondylitis Disease Activity Score (ASDAS) ≥2.1, received non-optimal treatment by non-steroidal anti-inflammatory drugs and were biologic-naive.

interventions(1) MAIN OUTCOME: Percentage of patients with a ≥30% improvement on the ASAS-Health Index (ASAS-HI). Other efficacy outcomes and adverse events were recorded. A health economic evaluation was performed. STATISTICAL ANALYSIS: Two-level mixed models were used to estimate efficacy outcomes. Cost-effectiveness was assessed by the incremental cost per quality-adjusted life-year (QALY) gained for TC/T2T versus UC.

results160 patients were included (80/group). Mean (SD) age was 37.9 (11.0) years and disease duration was 3.7 (6.2) years; 51.2% were men. ASDAS at inclusion was 3.0 (0.7), and ASAS-HI was 8.6 (3.7). ASAS-HI improved by ≥30% in 47.3% of the TC/T2T arm and in 36.1% of those receiving UC (non-significant). All secondary efficacy outcomes were more frequent in the TC/T2T arm, although not all statistically significant. Safety was similar in both arms. From a societal perspective, TC/T2T resulted in an additional 0.04 QALY, and saved €472 compared with UC.

conclusionTC/T2T was not significantly superior to UC for the primary outcome, while many secondary efficacy outcomes favoured it, had a similar safety profile and was favourable from a societal health economic perspective. TRIAL REGISTRATION NUMBER: NCT03043846.

Indexed as

Patient Care PlanningAdultAntirheumatic AgentsBiological ProductsCost-Benefit AnalysisFemaleHumansMaleMiddle AgedQuality-Adjusted Life YearsSpondylarthropathiesTreatment OutcomeAntirheumatic AgentsBiological Productsankylosinghealthcareoutcome and process assessmentspondylitistherapeutics

Identifiers

PMID33958325
PMCPMC8522451

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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.