Evidence map›Paper›PMID 27713619›Full record

ReviewDrug design, development and therapy2016

Spotlight on sirukumab for the treatment of rheumatoid arthritis: the evidence to date.

Pietro Enea Lazzerini, Pier Leopoldo Capecchi, Giacomo Maria Guidelli, Enrico Selvi, Maurizio Acampa, Franco Laghi-Pasini

Open access · goldAbstract readReview
In one paragraph

Review in Drug design, development and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Internists feel the rhythm.Internal and emergency medicine · 2020
    Article
  6. Review
  7. Review
  8. Review
  9. Selected cytokine pathways in rheumatoid arthritis.Seminars in immunopathology · 2017
    Review
  10. 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

6 authors at 1 institution in 1 country.

Pietro Enea LazzeriniDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena.
Pier Leopoldo CapecchiDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena.
Giacomo Maria GuidelliDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena.
Enrico SelviDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena.
Maurizio AcampaStroke Unit, University Hospital of Siena, Siena, Italy.
Franco Laghi-PasiniDepartment of Medical Sciences, Surgery and Neurosciences, University of Siena.
University of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease primarily affecting synovial joints and is characterized by persistent high-grade systemic inflammation. Proinflammatory cytokines, particularly interleukin-6 (IL-6), are of crucial importance in the pathogenesis of the disease, driving both joint inflammation and extra-articular comorbidities. Tocilizumab, a humanized IL-6 receptor-inhibiting monoclonal antibody, has been the first, and, to date, the only, IL-6 inhibitor approved for the treatment of RA. Many studies have demonstrated the potency and effectiveness of tocilizumab in controlling disease activity and radiological progression of RA. These successful results have encouraged the development of novel IL-6 inhibitors, among which a promising agent is sirukumab (SRK), a human anti-IL-6 monoclonal antibody currently under evaluation in Phase II/III studies in patients with RA, systemic lupus erythematosus, giant-cell arteritis, and major depressive disorder. The evidence to date indicates SRK as an effective and well-tolerated new therapeutic tool for patients with active RA, with some preliminary data suggesting a specific beneficial impact on relevant systemic complications associated with the disease, such as depression and cardiovascular disease. Conversely, although pathophysiological considerations make plausible the hypothesis that IL-6 blockade with SRK may also be beneficial in the treatment of many diseases other than RA (either autoimmune or not), available clinical data in patients with systemic lupus erythematosus do not seem to support this view, also giving rise to potentially relevant concerns about drug safety. If large Phase III clinical trials currently in progress in patients with RA confirm the efficacy and tolerability of SRK, then in the long term, this drug could, in the near future, occupy a place in the treatment of the disease, potentially also opening the doors to a more extended use of SRK in a wide range of disorders in which IL-6 plays a key pathogenic role.

Indexed as

Interleukin-6 InhibitorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedArthritis, RheumatoidHumansInterleukin-6Lupus Erythematosus, SystemicMajor Depressive DisorderReceptors, Interleukin-6Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedInterleukin-6Interleukin-6 InhibitorsReceptors, Interleukin-6sirukumabcardiovascular diseaseinterleukin-6rheumatoid arthritissirukumabsystemic lupus erythematosustocilizumab

Identifiers

PMID27713619
PMCPMC5044992
OpenAlexW2526047368

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.