Evidence map›Paper›PMID 36140230›Full record

ArticleBiomedicines2022

Subcutaneous Infliximab [CT-P13], a True Biologic 2.0. Real Clinical Practice Multicentre Study.

Jose M Huguet, Victor García-Lorenzo, Lidia Martí, Jose María Paredes, Jose Joaquin Ramírez, Miguel Pastor, Lucia Ruiz, Ana Sanahuja, Pilar Timoneda, Laura Sanchís and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

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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

12 authors at 5 institutions in 1 country.

Jose M HuguetGastroenterology Department, Hospital General Universitario de Valencia, 46014 Valencia, Spain.ORCID 0000-0001-6486-1262
Victor García-LorenzoGastroenterology Department, Hospital General Universitario de Valencia, 46014 Valencia, Spain.ORCID 0000-0002-4662-2070
Lidia MartíGastroenterology Department, Hospital Francesc de Borja de Gandia, 46702 Valencia, Spain.
Jose María ParedesGastroenterology Department, Hospital Universitario Doctor Peset, 46017 Valencia, Spain.
Jose Joaquin RamírezGastroenterology Department, Hospital Lluis Alcanyis de Xativa, 46800 Valencia, Spain.
Miguel PastorGastroenterology Department, Hospital Lluis Alcanyis de Xativa, 46800 Valencia, Spain.
Lucia RuizGastroenterology Department, Hospital General Universitario de Valencia, 46014 Valencia, Spain.
Ana SanahujaGastroenterology Department, Hospital Clínico Universitario de Valencia, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0003-2798-7610
Pilar TimonedaClinical Analysis Department, Hospital General Universitario de Valencia, 46014 Valencia, Spain.
Laura SanchísGastroenterology Department, Hospital de Sagunto, 46520 Valencia, Spain.
Gloria Alemany PérezGastroenterology Department, Hospital Francesc de Borja de Gandia, 46702 Valencia, Spain.
Marta Maia Boscá-WattsGastroenterology Department, Hospital Clínico Universitario de Valencia, University of Valencia, 46010 Valencia, Spain.
Hospital General Universitario De Valencia · ESHospital Universitario Lluís Alcanyís · ESUniversitat de València · ESHospital de Sagunto · ESHospital Universitario Doctor Peset · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, is characterized by chronic relapsing intestinal inflammation. There are few data on the efficacy and safety in clinical practice of infliximab (CT-P13) in subcutaneous formulation (SC) for the treatment of patients with IBD.

methodsMulticenter, prospective study of patients with IBD in clinical remission, who had their treatment changed from intravenous (IV) infliximab to SC. Two groups of patients were evaluated according to whether they were on IV infliximab treatment at standard or intensified doses before the switch.

resultsA total of 30 patients were on standard dosing and another 30 in intensified therapy. Treatment persistence in both groups at 6 months was greater than 95%. In both groups after the change, neither the biomarkers of inflammation nor the activity indices underwent significant changes at 3 and 6 months compared to the baseline value. Similarly, in both groups, infliximab trough levels showed a significant increase 3 and 6 months after the change to SC. No serious adverse events were registered.

conclusionsThe CT-P13 SC brings a new anti-TNF era. Achieving much higher drug levels that are constant over time opens new paths to explore the management of patients with IBD: less immunogenicity, better perianal disease control and higher achievement of mucosal healing.

Indexed as

Crohn’s diseaseCT-P13inflammatory bowel diseaseinfliximabinfliximab trough levelsubcutaneousswitchulcerative colitis

Identifiers

PMID36140230
PMCPMC9495964
OpenAlexW4293686761

What OpenQuestion holds

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LicenceCC BY
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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.