Evidence map›Paper›PMID 33123205›Full record

ArticleDrugs in context2020

Upadacitinib

Karel Pavelka, Zoltán Szekanecz, Nemanja Damjanov, Branimir Anić, Matija Tomšič, Vadim Mazurov, Marija Maksimovic, Orsolya Nagy, Jerzy Świerkot, Tzvetanka Petranova and 5 more

Open access · goldAbstract read
In one paragraph

Article in Drugs in context, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
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

15 authors at 12 institutions in 12 countries.

Karel PavelkaInstitute of Rheumatology and Department of Rheumatology, Charles University, Prague, Czech Republic.
Zoltán SzekaneczDivision of Rheumatology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Nemanja DamjanovUniversity of Belgrade School of Medicine, Institute of Rheumatology, Belgrade, Serbia.
Branimir AnićDivision of Clinical Immunology and Rheumatology, Department of Internal Medicine, University of Zagreb School of Medicine, Zagreb, Croatia.
Matija TomšičDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Vadim MazurovNorth-Western State Medical University named after I.I. Mechnikov, St Petersburg, Russia.
Marija MaksimovicAbbVie Biopharmaceuticals GmbH, Belgrade, Serbia.
Orsolya NagyAbbVie Global Medical Affairs, Rheumatology, Budapest, Hungary.
Jerzy ŚwierkotDepartment of Rheumatology and Internal Medicine, Wroclaw Medical University, Wroclaw, Poland.
Tzvetanka PetranovaDepartment of Rheumatology, UMHAT St.Iv.Rilsky, Medical University, Sofia, Bulgaria.
Tiina VeldiEast-Tallinn Central Hospital, Tallinn, Estonia.
Asta BaranauskaitėDepartment of Rheumatology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Catalin CodreanuCenter of Rheumatic Diseases, University of Medicine and Pharmacy, Bucharest, Romania.
Daina AndersoneP. Stradins Clinical University Hospital, Riga, Latvia.
Roy FleischmannUniversity of Texas Southwestern Medical Center, Metroplex Clinical Research Center, Dallas, TX, USA.
Charles University · CZEast Tallinn Central Hospital · EELithuanian University of Health Sciences · LTLjubljana University Medical Centre · SIMedical University of Sofia · BGNorth-Western State Medical University named after I.I. Mechnikov · RUPauls Stradiņš Clinical University Hospital · LVSouthwestern Medical Center · USUniversity of Belgrade · RSUniversity of Debrecen · HUUniversity of Zagreb · HRWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the randomized, phase III, global SELECT-COMPARE study, upadacitinib 15 mg demonstrated efficacy at week 12

methodsPatients were randomized 2:2:1 to upadacitinib 15 mg once daily, placebo, or adalimumab 40 mg every other week, and continued MTX. Efficacy and safety were assessed through 48 weeks. Primary endpoints were the achievement of ≥20% improvement in American College of Rheumatology response criteria and Disease Activity Score in 28 joints with C-reactive protein <2.6 responses at week 12 for upadacitinib

resultsA total of 596 patients from 12 CEE countries were randomized. At week 12, a numerically greater proportion of patients receiving upadacitinib

conclusionConsistent with the global population of patients with rheumatoid arthritis and an inadequate response to MTX, in CEE patients, upadacitinib 15 mg demonstrated clinical and functional improvements

Indexed as

Eastern Europerheumatoid arthritissafetytreatment efficacyupadacitinib

Identifiers

PMID33123205
PMCPMC7574850
OpenAlexW3094058107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.