Evidence map›Paper›PMID 32100960›Full record

ArticleClinical and translational science2020

Exposure-Response Relationship of Certolizumab Pegol and Achievement of Low Disease Activity and Remission in Patients With Rheumatoid Arthritis.

Stéphane Paul, Hubert Marotte, Arthur Kavanaugh, Philippe Goupille, Tore K Kvien, Marc de Longueville, Denis Mulleman, William J Sandborn, Niels Vande Casteele

4 registry-linked trialsAbstract read
In one paragraph

Article in Clinical and translational science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT00152386 phase3completednot on this map

A Phase III Multicentre, Double Blind, Placebo-controlled, Parallel Group 52-week Study to Assess the Efficacy and Safety of 2 Dose Regimens of Lyophilised CDP870 as Additional Medication to Methotrexate in the Treatment of Signs and Symptoms and Preventing Structural Damage in Patients With Active Rheumatoid Arthritis Who Have an Incomplete Response to Methotrexate

TypeinterventionalSponsorUCB PharmaRan2005 to 2006Enrolled950ConditionsRheumatoid ArthritisArmsCertolizumab pegol (CDP870)
NCT00160602 phase3completednot on this map

A Phase III Multi-center, Double-blind, Placebo-controlled, Parallel Group 24-Week Study to Assess the Efficacy and Safety of Two Dose Regimens of Liquid Certolizumab Pegol as Additional Medication to Methotrexate in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis Who Have an Incomplete Response to Methotrexate.

TypeinterventionalSponsorUCB PharmaRan2005 to 2006Enrolled590ConditionsRheumatoid ArthritisArmsCertolizumab Pegol
NCT00160641 phase3completednot on this map

A Phase III Multi-center, Open-label, Follow-up Study, to Assess the Safety and Efficacy of Liquid Certolizumab Pegol as Additional Medication to Methotrexate, in the Treatment of Signs and Symptoms and in the Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis Who Participated in Study CDP870-050

TypeinterventionalSponsorUCB PharmaRan2005 to 2012Enrolled567ConditionsRheumatoid ArthritisArmsCertolizumab Pegol
NCT00175877 phase3completednot on this map

A Phase III Multi-centre, Open-label, follow-on Study to CDP870-027, to Assess the Efficacy and Safety of Lyophilized CDP870 an Engineered Human Anti-TNF PEG Conjugate, as Additional Medication to Methotrexate, in the Treatment of Signs and Symptoms and Preventing Structural Damage in Patients With Active Rheumatoid Arthritis

TypeinterventionalSponsorUCB PharmaRan2005 to 2012Enrolled857ConditionsRheumatoid ArthritisArmsCertolizumab Pegol
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  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

9 authors.

Stéphane PaulDepartment of Immunology, CIC1408, GIMAP EA3064, Université Jean Monnet, Saint Étienne, France.ORCID 0000-0002-8830-4273
Hubert MarotteDepartment of Rheumatology, SAINBOISE AINBIOSE INSERM 1059, University of Lyon, Saint-Étienne, France.
Arthur KavanaughDivision of Rheumatology, Allergy & Immunology, University of California San Diego School of Medicine, La Jolla, California, USA.
Philippe GoupilleDepartment of Rheumatology, University Hospital of Tours, EA 7501, Tours, France.
Tore K KvienDepartment of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.
Marc de LonguevilleUCB Pharma, Brussels, Belgium.
Denis MullemanDepartment of Rheumatology, University Hospital of Tours, EA 7501, Tours, France.
William J SandbornDepartment of Medicine, University of California San Diego, La Jolla, California, USA.
Niels Vande CasteeleDepartment of Medicine, University of California San Diego, La Jolla, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-tumor necrosis factor (anti-TNF) drugs are often prescribed for the treatment of rheumatoid arthritis (RA) and other immune-mediated inflammatory diseases. Although this treatment has been shown to be effective in many patients, up to 40% of patients do not achieve disease control. Drug concentration in plasma may be a factor affecting the observed variability in therapeutic response. In this study, we aimed to identify the plasma concentrations of the anti-TNF certolizumab pegol (CZP), associated with improvement in disease activity in patients with RA. Data were pooled from three randomized, controlled clinical trials with a combined total of 1,935 patients analyzed. Clinical outcomes of low disease activity (LDA) and remission were defined as Disease Activity Score in 28 joints with C-reactive protein (DAS28(CRP)) ≤ 2.7 and < 2.3, respectively. Quartile analysis results indicated that there may be an exposure-response relationship between CZP concentration and LDA/remission outcomes at weeks 12 and 24; the association was strongest for LDA (P < 0.05). Receiver operating characteristic (ROC) analysis showed that CZP concentrations ≥ 28.0 μg/ml at week 12, and ≥ 17.6 μg/ml at week 24, were associated with a greater likelihood of achieving LDA/remission outcomes. Although confirmatory studies are warranted to define the optimal CZP therapeutic range at weeks 12 and 24, these data indicate that CZP concentrations may be associated with improvement of disease activity.

Indexed as

AdultAgedAntirheumatic AgentsArthritis, RheumatoidCertolizumab PegolDose-Response Relationship, DrugDrug MonitoringFeasibility StudiesFemaleHumansMaleMiddle AgedRandomized Controlled Trials as TopicROC CurveSeverity of Illness IndexTreatment OutcomeAntirheumatic AgentsCertolizumab PegolTNF protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID32100960
PMCPMC7359948

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Registered trials

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.