Evidence map›Paper›PMID 26048626›Full record

ReviewRheumatology international2015

Canakinumab efficacy and long-term tocilizumab administration in tumor necrosis factor receptor-associated periodic syndrome (TRAPS).

Francesco La Torre, Maurizio Muratore, Antonio Vitale, Fulvio Moramarco, Laura Quarta, Luca Cantarini

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Rheumatology international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 51 citations in OpenAlex.

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  20. [Causes and treatment of systemic amyloidosis].Zeitschrift fur Rheumatologie · 2016
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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

6 authors at 2 institutions in 1 country.

Francesco La TorreDepartment of Paediatrics, Antonio Perrino Hospital, Brindisi, Italy. latorre_francesco@virgilio.it.
Maurizio MuratoreDepartment of Rheumatology, Hospital Galateo, San Cesario di Lecce, Italy.
Antonio VitaleResearch Center of Systemic Autoinflammatory Diseases and Behcet's Disease, Policlinico Le Scotte, University of Siena, Siena, Italy.
Fulvio MoramarcoDepartment of Paediatrics, Antonio Perrino Hospital, Brindisi, Italy.
Laura QuartaDepartment of Rheumatology, Hospital Galateo, San Cesario di Lecce, Italy.
Luca CantariniResearch Center of Systemic Autoinflammatory Diseases and Behcet's Disease, Policlinico Le Scotte, University of Siena, Siena, Italy.
Ospedale A. Perrino · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominantly inherited autoinflammatory disease caused by mutations in the TNFRSF1A gene. Treatment is aimed at preventing acute disease attacks, improving quality of life, and preventing long-term complications such as systemic reactive amyloidosis. Biologic agents have significantly improved TRAPS management. In particular, interleukin 1 (IL-1) inhibition either with the recombinant IL-1 receptor antagonist anakinra or with the human IgG1 anti-IL-1β monoclonal antibody canakinumab has recently shown to induce a prompt and stable disease remission. Conversely, the successful experience with IL-6 inhibition is nowadays limited to a single patient. Anyway, introduction of new treatment options for patients requiring a lifelong therapy is desirable. We describe two TRAPS patients (son and father) successfully treated with canakinumab and tocilizumab, respectively. In particular, we highlight the clinical and laboratory efficacy as well as the good safety profile of tocilizumab during a 42-month follow-up period.

Indexed as

AdultAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedChild, PreschoolDNA Mutational AnalysisDrug Administration ScheduleFeverGenetic Predisposition to DiseaseHereditary Autoinflammatory DiseasesHumansImmunosuppressive AgentsMaleMutationPhenotypeReceptors, Tumor Necrosis Factor, Type ITime FactorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedcanakinumabImmunosuppressive AgentsReceptors, Tumor Necrosis Factor, Type ITNFRSF1A protein, humantocilizumabAutoinflammatory disordersCanakinumabFollow-upTherapyTocilizumab

Identifiers

PMID26048626
OpenAlexW594828834

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.