Evidence map›Paper›PMID 35312895›Full record

ArticleClinical rheumatology2022

Improvement in disease activity among patients with rheumatoid arthritis who switched from intravenous infliximab to intravenous golimumab in the ACR RISE registry.

John Tesser, Iris Lin, Natalie J Shiff, Soumya D Chakravarty, Gabriela Schmajuk, Nevin Hammam, Sheetal Desai

Open access · hybridAbstract read
In one paragraph

Article in Clinical rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 31% 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.

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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 5 institutions in 2 countries.

John TesserArizona Arthritis & Rheumatology Associates, 4550 E. Bell Road, Suite 172, Phoenix, AZ, 85032, USA. jtesser1@cox.net.ORCID http://orcid.org/0000-0002-2706-7171
Iris LinJanssen Scientific Affairs, LLC, Horsham, PA, USA.ORCID http://orcid.org/0000-0003-0176-4435
Natalie J ShiffJanssen Scientific Affairs, LLC, Horsham, PA, USA.ORCID http://orcid.org/0000-0002-7410-9709
Soumya D ChakravartyJanssen Scientific Affairs, LLC, Horsham, PA, USA.ORCID http://orcid.org/0000-0001-7957-838X
Gabriela SchmajukUniversity of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-2687-5043
Nevin HammamUniversity of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-7754-5581
Sheetal DesaiUniversity of California, Irvine, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-7180-8387
Janssen (United States) · USUniversity of California, San Francisco · USArthritis and Rheumatism Associates · USSaskatchewan Health Authority · CAUniversity of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infliximab and golimumab are intravenously (IV) administered tumor necrosis factor inhibitors approved to treat moderate-to-severe rheumatoid arthritis (RA) with concomitant methotrexate. Owing to differences in biologic construct, patients with IV-infliximab treatment failure may benefit from switching to IV-golimumab. Utilizing the ACR's Rheumatology Informatics System for Effectiveness (RISE), a large electronic health records registry based in the USA, we assessed RA disease activity in patients switching from IV-infliximab to IV-golimumab. This retrospective, longitudinal, single-arm study included adults (≥ 18 years) with ≥ 1 RA diagnosis code between 2014 and 2018 and ≥ 1 IV-infliximab prescription within 6 months of a new IV-golimumab order (index date). Longitudinal assessments of disease activity using the Clinical Disease Activity Index (CDAI) were calculated in patients continuing IV-golimumab for 6-9- and 9-12-months post-switch. Paired t-tests evaluated significance of mean improvements during the follow-up periods. Most RA patients with disease activity assessments during the 6-month follow-up (N = 100; mean age: 65.3 years; 81% female; 74% white) demonstrated moderate-to-high disease activity (CDAI: 73% [38/52]) at enrollment. On average, patients showed significant improvement in disease activity within 6-9 months of switching; mean CDAI scores improved from 21.3 to 14.1 (p < 0.0001) and were durable through 9-12 months of treatment. Real-world patients with moderate-to-high disease activity who switched from IV-infliximab to IV-golimumab demonstrated significant and sustained improvements post-switch as measured by the CDAI. Key Points • This study used real-world data from the Rheumatology Informatics System for Effectiveness (RISE) registry to evaluate the efficacy of directly switching from intravenous (IV)-infliximab to IV-golimumab to control rheumatoid arthritis (RA) disease activity. • Most IV-infliximab patients had moderate-to-high disease activity at the time of the switch. • On average, IV-golimumab was effective in improving RA disease activity after switching from IV-infliximab as measured by the Clinical Disease Activity Index. • These data suggest that real-world RA patients with persistent symptoms despite treatment with IV-infliximab may realize improved disease control with a switch to IV-golimumab.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidRheumatologyAdultAgedAntibodies, MonoclonalFemaleHumansInfliximabInformaticsMaleRegistriesRetrospective StudiesTreatment OutcomeAntibodies, MonoclonalAntirheumatic AgentsgolimumabInfliximabDisease activityIntravenous golimumabIntravenous infliximabRegistryRheumatoid arthritisTumor necrosis factor

Identifiers

PMID35312895
PMCPMC9287251
OpenAlexW4220784230

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.