Evidence map›Paper›PMID 40166776›Full record

ArticleTherapeutic advances in musculoskeletal disease2025

Primary non-response in inflammatory arthritis treated with biologics and targeted therapies in daily clinical practice.

Leticia Leon, Dalifer Freites-Nuñez, Esther Toledano, Gloria Candelas, Cristina Martinez, María Rodríguez-Laguna, Benjamín Fernández-Gutiérrez, Lydia Abasolo

Abstract read
In one paragraph

Article in Therapeutic advances in musculoskeletal disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 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.

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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
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.

Leticia LeonMusculoskeletal Pathology Group, Rheumatology Department, IdISSC, Hospital Clínico San Carlos, c\Prof, Martín Lagos s/n, Madrid 28040, Spain.ORCID https://orcid.org/0000-0001-7142-0545
Dalifer Freites-NuñezRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Esther ToledanoRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Gloria CandelasRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Cristina MartinezRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
María Rodríguez-LagunaRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Benjamín Fernández-GutiérrezRheumatology Department and IdISSC, Hospital Clínico San Carlos, Madrid, Spain Medicine Department, Universidad Complutense de Madrid, Madrid, Spain.ORCID https://orcid.org/0000-0002-6126-8786
Lydia AbasoloMusculoskeletal Pathology Group, Rheumatology Department, IdISSC, Hospital Clínico San Carlos, Madrid, Spain.ORCID https://orcid.org/0000-0001-8152-0478

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Switching between therapies is a recommended strategy for rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients who experience treatment failure; moreover, data on switching due to primary non-response and subsequent failures are limited. Objectives: To obtain information from clinical practice regarding failures due to primary non-response in patients on biologic and target synthetic disease-modifying antirheumatic drugs (ts/bDMARDs), assessing the incidence rate (IR) of switching due to primary non-response and risk of subsequent treatment failure by cycling compared to swapping. Design: A longitudinal retrospective study, spanning from 2007 to 2022, was conducted on patients with RA or PsA treated with ts/bDMARDs at an outpatient rheumatology clinic. Methods: The main outcomes were as follows: (1) ts/bDMARD failure due to primary non-response and (2) subsequent discontinuation of prescribed ts/bDMARD due to lack of efficacy. The independent variable was switching between classes compared to switching within class. As covariates, clinical, sociodemographic, clinical, and treatments were considered. To estimate ts/bDMARDs switching rates, survival techniques were used, expressing the IR per 100 patients * year with their 95% confidence interval. Cox multivariate regression analyses were run to assess the role of switching between/within class in the subsequent treatment failure. Results: In total, 327 patients were included. Of these, 50 patients in 77 treatment courses developed primary non-response with an IR of 4.25 (3.4-5.3). The IR was quite similar between RA and PsA, higher in women, and in those who started ts/bDMARDs after 2018. In those with primary non-response, there were 42 subsequent treatment failures with an IR of 26.38 (19.49-35.69). The multivariate model showed that cycling increased the risk of subsequent failure compared to swapping (hazard ratio: 2 (1.1-3.77), Conclusion: This study provides support to consider swapping a better alternative rather than cycling after primary non-response.

Indexed as

biologic and target synthetic disease-modifying antirheumatic drugsprimary non-responsepsoriatic arthritisrheumatoid arthritisswitching

Identifiers

PMID40166776
PMCPMC11956518

What OpenQuestion holds

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Registered trials

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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.