Evidence map›Paper›PMID 28331376›Full record

ArticleOpen access rheumatology : research and reviews2017

Long-term safety and efficacy of biosimilar infliximab among patients with inflammatory arthritis switched from reference product.

Abuelmagd Abdalla, Niamh Byrne, Richard Conway, Thomas Walsh, Geraldine Mannion, Michael Hanly, Miriam O'Sullivan, Ann Maria Curran, John J Carey

Open access · goldAbstract read
In one paragraph

Article in Open access rheumatology : research and reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 6 pooled it
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 6 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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  6. Biosimilarity and Interchangeability: Principles and Evidence: A Systematic Review.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2018
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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

9 authors at 1 institution in 1 country.

Abuelmagd AbdallaDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Niamh ByrneDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Richard ConwayDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Thomas WalshDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Geraldine MannionDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Michael HanlyDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Miriam O'SullivanDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
Ann Maria CurranDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
John J CareyDepartment of Rheumatology, Galway University Hospitals, Galway, Ireland.
University Hospital Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the efficacy and safety of the biosimilar infliximab in adult patients with inflammatory arthritis switched from reference product in our center. PATIENTS AND

methodsIn April 2014, patients attending our rheumatology service for infliximab infusions were switched from reference product to the biosimilar infliximab following consent and hospital approval.

resultsAround 34 patients with inflammatory arthritis were switched from reference product to biosimilar infliximab in 2014: 50% female, mean age 55 years (standard deviation=12.9), mean disease duration 14.79 years (9.7), median duration on infliximab 57 months, and two-thirds on oral disease-modifying antirheumatic drugs. There was no difference in efficacy or safety in the first 6 months of therapy. By the end of 2015, the mean follow-up on biosimilar infliximab was 15.8 (standard deviation=6.3) months. Our results showed no significant difference in Health Assessment Questionnaire score, patient global assessment of disease activity, number of disease flares, or the medication dose between the originator and the biosimilar infliximab. However, reported pain and C-reactive protein values were significantly higher during the longer follow-up period (

conclusionOur patients experienced similar efficacy and safety for managing their arthritis with the biosimilar infliximab as the reference product infliximab, but at a much lower cost.

Indexed as

adultbiologic therapybiosimilar exchangeinfliximabrheumatic diseases

Identifiers

PMID28331376
PMCPMC5349501
OpenAlexW2593580677

What OpenQuestion holds

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LicenceCC BY-NC
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.