Evidence map›Paper›PMID 32107666›Full record

SynthesisClinical rheumatology2020

A systematic review and network meta-analysis of current and investigational treatments for active ankylosing spondylitis.

A Deodhar, S D Chakravarty, C Cameron, S Peterson, R Hensman, S Fogarty, P Spin, S Kafka, S Nair, L S Gensler

Open access · hybridAbstract readNetwork Meta-AnalysisSystematic Review
In one paragraph

Synthesis in Clinical rheumatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Efficacy and Safety of Intravenous Golimumab in Ankylosing Spondylitis Patients With Early and Late Disease Through One Year of the GO-ALIVE Study.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases · 2022
    Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Immunosuppression in Rheumatologic and Auto-immune Disease.Handbook of experimental pharmacology · 2022
    Article
  14. 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

10 authors at 4 institutions in 2 countries.

A DeodharOregon Health & Science University, Portland, OR, USA. deodhara@ohsu.edu.ORCID https://orcid.org/0000-0002-2130-1246
S D ChakravartyJanssen Scientific Affairs, LLC, Horsham, PA, USA.
C CameronCornerstone Research Group Inc., Burlington, Ontario, Canada.
S PetersonJanssen Global Services, LLC, Horsham, PA, USA.
R HensmanCornerstone Research Group Inc., Burlington, Ontario, Canada.
S FogartyCornerstone Research Group Inc., Burlington, Ontario, Canada.
P SpinCornerstone Research Group Inc., Burlington, Ontario, Canada.
S KafkaJanssen Scientific Affairs, LLC, Horsham, PA, USA.
S NairJanssen Pharmaceutica NV, Turnhoutseweg 30, 2340, Beerse, Belgium.
L S GenslerUniversity of California San Francisco, San Francisco, CA, USA.
Janssen (United States) · USJanssen (Belgium) · BEOregon Health & Science University · USUniversity of California, San Francisco · US

Funding

Janssen Scientific Affairs, LLC 00000
6 · The paper itself

Abstract

objectiveTo compare the relative efficacy of current and investigational biologic and oral small molecule (OSM) treatments for active ankylosing spondylitis (AS).

methodsA systematic literature review was conducted to identify all phase 2/3 randomized trials of interest in patients with AS. Outcomes assessed were ≥ 20% improvement in the Assessment of Spondyloarthritis International Society Criteria (ASAS20) and change from baseline in Bath Ankylosing Spondylitis Functional Index (BASFI) and C-reactive protein (CRP) at weeks 12-16. Bayesian network meta-analyses were conducted for outcomes using a random effects model. Baseline-risk adjustment was also conducted to account for differences in placebo response across studies. Surface Under the Cumulative Ranking curve (SUCRA) values are reported, reflecting the relative probability that intervention was the best of all interventions.

resultsThe investigational agent tofacitinib 5 mg was the top-ranked treatment (SUCRA, 93%) for ASAS20 response, followed by intravenous (IV) golimumab 2 mg/kg (90%). Golimumab IV 2 mg/kg and infliximab 5 mg/kg were the top two ranked treatments for change from baseline in BASFI (golimumab IV, 81%; infliximab, 80%) and change from baseline in CRP (infliximab, 90%; golimumab IV, 82%).

conclusionsTwo approved therapies (golimumab IV, infliximab) and one investigational product ranked highest for efficacy in AS. Key Points • Although golimumab IV, infliximab, and tofacitinib ranked highest for efficacy in AS, differences in efficacy between approved and investigational therapies were not statistically significant.

Indexed as

Spondylitis, AnkylosingTherapies, InvestigationalTumor Necrosis Factor InhibitorsAdministration, IntravenousAntibodies, MonoclonalBayes TheoremHumansInfliximabRandomized Controlled Trials as TopicAntibodies, MonoclonalgolimumabInfliximabTumor Necrosis Factor InhibitorsAnkylosing spondylitisBiologicIntravenous golimumabNetwork meta-analysisSystematic review

Identifiers

PMID32107666
PMCPMC7338808
OpenAlexW3007126479

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.