Evidence map›Paper›PMID 35071559›Full record

ArticleWorld journal of clinical cases2021

Real-world data on the infliximab biosimilar CT-P13 (Remsima

Jose María Huguet, Xavier Cortés, Marta Maia Bosca-Watts, Marian Aguas, Nuria Maroto, Lidia Martí, Cirilo Amorós, Jose María Paredes

Open access · diamondAbstract read
In one paragraph

Article in World journal of clinical cases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

8 authors at 8 institutions in 1 country.

Jose María HuguetDepartment of Gastroenterology, General University Hospital of Valencia, Valencia 46014, Spain. josemahuguet@gmail.com.
Xavier CortésDepartment of Gastroenterology, Hospital de Sagunto, Sagunto 46520, Spain.
Marta Maia Bosca-WattsDepartment of Gastroenterology, Hospital Clinico Universitario de Valencia, Valencia 46010, Spain.
Marian AguasDepartment of Gastroenterology, Hospital Universitario y Politecnico la Fe de Valencia, Valencia 46026, Spain.
Nuria MarotoDepartment of Gastroenterology, Hospital de Manises, Manises 46940, Spain.
Lidia MartíDepartment of Gastroenterology, Hospital Comarcal Francesc de Borja, Gandia 46702, Spain.
Cirilo AmorósDepartment of Gastroenterology, Hospital Arnau de Vilanova de Valencia, Valencia 46015, Spain.
Jose María ParedesDepartment of Gastroenterology, Hospital Universitario Doctor Peset de Valencia, Valencia 46017, Spain.
Hospital Arnau de Vilanova · ESHospital Clínico Universitario de Valencia · ESHospital Comarcal de Inca · ESHospital de Manises · ESHospital de Sagunto · ESHospital General Universitario De Valencia · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario Doctor Peset · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, biological therapies have revolutionized the management of inflammatory bowel disease (IBD); however, they are expensive. The development of biosimilar products has allowed us to reduce healthcare costs and improve patients' access to these treatments. Although various studies support the similarity between infliximab and its biosimilar CT-P13 in terms of efficacy and safety, there are unmet needs regarding research on these agents in the context of IBD.

aimTo analyze clinical response rates to CT-P13 and adverse events in IBD patients treated in real-life practice.

methodsAn observational, prospective, multicenter study of IBD patients treated with CT-P13 in clinical practice who were naïve to biological treatments or failed to respond to other anti-tumor necrosis factor drugs or had switched from infliximab originator was carried out. No diagnostic or follow-up interventions were conducted on patients outside usual clinical practice. The primary endpoints were clinical response rates and number of adverse events. The primary efficacy variable was the proportion of patients who were in clinical remission and/or had a clinical response at 3, 6, 9, and 12 mo.

resultsA total of 220 IBD patients treated with CT-P13 (Remsima

conclusionCT-P13 is an effective and safe infliximab biosimilar for the treatment of IBD in real-life practice and may be a valid and attractive alternative for the treatment of IBD.

Indexed as

BiosimilarCrohn’s diseaseCT-P13Inflammatory bowel diseaseInfliximabUlcerative colitis

Identifiers

PMID35071559
PMCPMC8717518
OpenAlexW4200411569

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.