Evidence map›Paper›PMID 42064587›Full record

ArticleRheumatology advances in practice2026

Decision on Optimal Combinatorial Therapies in Immune-mediated inflammatory diseases using Systems approaches (DocTIS): protocol for a single-arm, adaptive basket trial in rheumatoid and psoriatic arthritis.

Rory Sheppard, Myrsini Gianatsi, Ian Thomas, Sophie King, David Gillespie, Philip Pallmann, Sara Marsal Barril, Ernest Choy

Abstract read
In one paragraph

Article in Rheumatology advances in practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Rory SheppardCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.ORCID https://orcid.org/0000-0001-9571-8274
Myrsini GianatsiCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.ORCID https://orcid.org/0000-0003-3664-4302
Ian ThomasCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.
Sophie KingCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.
David GillespieCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.ORCID https://orcid.org/0000-0002-6934-2928
Philip PallmannCentre for Trials Research, College of Biomedical & Life Sciences, Cardiff University, Cardiff, UK.ORCID https://orcid.org/0000-0001-8274-9696
Sara Marsal BarrilRheumatology Department, Hospital Universitari Vall d'Hebron and Vall d'Hebron Institut de Recerca, Barcelona, Spain.ORCID https://orcid.org/0000-0001-5515-3854
Ernest ChoyDivision of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.ORCID https://orcid.org/0000-0003-4459-8609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Current treatments for rheumatoid arthritis (RA) and psoriatic arthritis (PsA) reduce disease activity but often fail to achieve sustained remission. The Decision on Optimal Combinatorial Therapies in Immune-mediated inflammatory diseases using Systems approaches (DocTIS) program has shown that additive anti-inflammatory effects in patients with arthritis can be achieved by combining tumour necrosis factor (TNF) and interleukin (IL)-6 inhibitor therapies. The goal was to provide proof-of-principle evaluation of whether combining TNF and IL-6 inhibitors shows a signal of activity on remission outcomes in RA and PsA. Methods: This is a single-arm, multicentre, adaptive basket trial recruiting 20 patients with RA and 20 with PsA and including 24 weeks of treatment and 10 weeks of safety follow-up. Eligible participants on TNF for ≥6 weeks will proceed with the addition of IL-6 inhibitor (tocilizumab) at 162 mg every 2 weeks for 8 weeks, increasing to weekly dosing in weeks 9-24 if well tolerated. The primary outcome is remission at 24 weeks (Clinical Disease Activity Index score ≤2.8 in RA and Disease Activity in PsA score <4). Secondary outcomes include safety, tolerability and disease activity assessments. Using Simon's two-stage design (80% power, one-sided α = 0.10), the trial aims to detect an increase in remission (10% to 30%). An interim futility analysis will occur after seven participants per basket reach 24 weeks. Conclusion: Findings from this proof-of-principle study will inform the feasibility and design of future randomised trials evaluating combination biologic therapy in inflammatory arthritis. Study registration: www.isrctn.com; ISRCTN50666516.

Indexed as

adaptive basket trialcombination biologic therapyimmune-mediated inflammatory diseasesinterleukin-6 inhibitionmultinational clinical trialmulti-omic analysisproof-of-principle studypsoriatic arthritisrheumatoid arthritistumour necrosis factor inhibitors

Identifiers

PMID42064587
PMCPMC13127746

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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.