Evidence map›Paper›PMID 28271234›Full record

Observational studyClinical rheumatology2017

Impact of prior biologic use on persistence of treatment in patients with psoriatic arthritis enrolled in the US Corrona registry.

Leslie R Harrold, Bradley S Stolshek, Sabrina Rebello, David H Collier, Alex Mutebi, Sally W Wade, Wendi Malley, Jeffrey D Greenberg, Carol J Etzel

Open access · hybridAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Clinical rheumatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 53 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

9 authors at 4 institutions in 1 country.

Leslie R HarroldCorrona, LLC, 325 Turnpike Road, Suite 325, Southborough, MA, 01772, USA. Leslie.Harrold@umassmed.edu.
Bradley S StolshekAmgen Inc., One Amgen Center Drive, Thousand Oaks, CA, 91320, USA.
Sabrina RebelloCorrona, LLC, 325 Turnpike Road, Suite 325, Southborough, MA, 01772, USA.
David H CollierAmgen Inc., One Amgen Center Drive, Thousand Oaks, CA, 91320, USA.
Alex MutebiAmgen Inc., One Amgen Center Drive, Thousand Oaks, CA, 91320, USA.
Sally W WadeWade Outcomes Research and Consulting, 136 U Street, Salt Lake City, UT, 84103, USA.
Wendi MalleyCorrona, LLC, 325 Turnpike Road, Suite 325, Southborough, MA, 01772, USA.
Jeffrey D GreenbergCorrona, LLC, 325 Turnpike Road, Suite 325, Southborough, MA, 01772, USA.
Carol J EtzelCorrona, LLC, 325 Turnpike Road, Suite 325, Southborough, MA, 01772, USA.
Ferro Solutions (United States) · USAmgen (United States) · USNew York University · USOutcomes Research Consortium · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriatic arthritis (PsA) is a chronic condition characterized by a diverse set of symptoms, from swollen joints to nail disease to skin disease. A variety of treatment options are available, including tumor necrosis factor inhibitors (TNFis). Little is known about treatment persistence in patients with PsA who initiate TNFi therapy, with and without prior biologic use. This study assessed persistence in these subgroups of patients with PsA and identified factors associated with persistence. This retrospective study utilized data from the Corrona registry of patients with PsA-with or without prior biologic experience-who initiated TNFi therapy between October 1, 2002, and March 21, 2013. Kaplan-Meier curves estimated median time to nonpersistence (discontinuation or switch to another biologic). Cox proportional hazards models identified factors associated with TNFi nonpersistence. A total of 1241 TNFi initiations were identified: 549 by biologic-naïve and 692 by biologic-experienced patients. Through 4 years of follow-up, more biologic-naïve than biologic-experienced patients remained persistent. Biologic-naïve patients had a greater mean time to nonpersistence compared with biologic-experienced patients: 32 vs 23 months (p = 0.0002). Moderate and high disease activities based on clinical disease activity index and disease duration were associated with persistence in both biologic-naïve and biologic-experienced patients. Additionally, in the biologic-experienced patients, the number of prior medications and skin disease were associated with persistence. The majority of patients with PsA in this study were persistent with their TNFi therapy; biologic-naïve patients had greater persistence compared with biologic-experienced patients. Predictors of persistence differed slightly between biologic-naïve and biologic-experienced patients.

Indexed as

Disease ProgressionAdultAntirheumatic AgentsArthritis, PsoriaticBiological ProductsFemaleHumansKaplan-Meier EstimateMaleMiddle AgedProportional Hazards ModelsRegistriesRetrospective StudiesSeverity of Illness IndexTime FactorsTreatment OutcomeAntirheumatic AgentsBiological ProductsTumor Necrosis Factor-alphaBiologicsDisease severityPersistencePsoriatic arthritisTumor necrosis factor inhibitors

Identifiers

PMID28271234
OpenAlexW2593480788

What OpenQuestion holds

Textmetadata
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.