Evidence map›Paper›PMID 30323555›Full record

ArticleBiologics : targets & therapy2018

A descriptive analysis of real-world treatment patterns of innovator (Remicade

Yusuf Yazici, Lin Xie, Adesuwa Ogbomo, Lorie A Ellis, Kavitha Goyal, Amanda Teeple, Ece A Mutlu, Ismail Simsek

Open access · goldAbstract read
In one paragraph

Article in Biologics : targets & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. 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

8 authors at 6 institutions in 2 countries.

Yusuf YaziciDepartment of Internal Medicine, Division of Rheumatology, New York University Hospital for Joint Diseases, New York, NY, USA.
Lin XieSTATinMED Research, Health Economics and Outcomes Research, Ann Arbor, MI, USA, aogbomo@statinmed.com.
Adesuwa OgbomoSTATinMED Research, Health Economics and Outcomes Research, Ann Arbor, MI, USA, aogbomo@statinmed.com.
Lorie A EllisJanssen Scientific Affairs, Real World Value and Evidence, Titusville, NJ, USA.
Kavitha GoyalJanssen Biotech Incorporated, Immunology Medical Affairs, Horsham, PA USA.
Amanda TeepleJassen Scientific Affairs, LLC, Health Economics and Outcomes Research, Horsham, PA, USA.
Ece A MutluRush University, Medical College, Department of Medicine, Chicago, IL, USA.
Ismail SimsekGuven Hospital, Department of Rheumatology, Ankara, Turkey.
Janssen (United States) · USSTATinMED (United States) · USGüven Hospital · TRJanssen Scientific Affairs (United States)New York University Langone Orthopedic Hospital · USRush University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBiosimilar IFX (CT-P13) received marketing approval in Turkey for treatment of rheumatologic diseases, including ankylosing spondylitis, psoriatic arthritis, rheumatoid arthritis (RA), inflammatory bowel disease (IBD), and psoriasis. Population data on real-world treatment patterns of CT-P13 following marketing approval in European countries are largely unreported. This study examined the prescribing and medication utilization patterns of innovator infliximab (IFX) and CT-P13 in Turkey for patients with RA or IBD naïve to either IFX. MATERIALS AND

methodsAdult patients with ≥1 diagnosis claim for RA or IBD and ≥1 claim for IFX or CT-P13 were identified in the Turkish Ministry of Health database during the following identification periods: 1 Oct 2014-30 May 2015 (RA) and 1 Oct 2014-31 Dec 2015 (IBD). Continuous medical and pharmacy coverage for ≥12 months before and after the date of the first dose (index) IFX or CT-P13 was also required. Separate analyses were done for each population.

resultsSeven hundred and seventy nine adult RA and 581 IBD patients met the selection criteria. The majority of RA (74%; n=575) and IBD patients (87%; n=504) were initiated on IFX. The average study observation period was 16 months for the RA and 12 months for the IBD population. Over the observation periods, discontinuation among RA patients occurred in 42% of IFX and 63% of CT-P13 while discontinuation in the IBD cohort occurred in 38% of IFX; and 62% of CT-P13.

conclusionIn this population-based study, more IFX-naïve RA and IBD patients were initially treated with IFX than CT-P13. Discontinuation and switching were observed more often and earlier among patients treated with CT-P13 regardless of disease state. Further studies are needed to understand the reasons for these observed differences.

Indexed as

discontinuationinflammatory bowel diseaserheumatoid arthritisswitch

Identifiers

PMID30323555
PMCPMC6174299
OpenAlexW2894038307

What OpenQuestion holds

Textmetadata
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.