Evidence map›Paper›PMID 35211430›Full record

ArticleFrontiers in pediatrics2022

The Safety and Efficacy of Tofacitinib in 24 Cases of Pediatric Rheumatic Diseases: Single Centre Experience.

Mikhail M Kostik, Rinat K Raupov, Evgeny N Suspitsin, Eugenia A Isupova, Ekaterina V Gaidar, Tatyana V Gabrusskaya, Maria A Kaneva, Ludmila S Snegireva, Tatyana S Likhacheva, Rimma S Miulkidzhan and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Recent updates in enthesitis-related arthritis.Rheumatology international · 2023
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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

17 authors at 3 institutions in 2 countries.

Mikhail M KostikHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Rinat K RaupovHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Evgeny N SuspitsinHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Eugenia A IsupovaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Ekaterina V GaidarHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Tatyana V GabrusskayaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Maria A KanevaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Ludmila S SnegirevaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Tatyana S LikhachevaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Rimma S MiulkidzhanLaboratory of the Molecular Oncology, N.N. Petrov's Institute of Oncology, Saint-Petersburg, Russia.
Artem V KosminLaboratory of the Molecular Oncology, N.N. Petrov's Institute of Oncology, Saint-Petersburg, Russia.
Anastasia V TumakovaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Vera V MasalovaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Margarita F DubkoHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Olga V KalashnikovaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Ivona AksentijevichInflammatory Disease Section, National Human Genome Research Institute, Bethesda, MD, United States.
Vyacheslav G ChasnykHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia.
Saint Petersburg State Pediatric Medical University · RUInstitute of Oncology NN Petrov · RUNational Human Genome Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

JAK-inhibitors are small molecules blocking the JAK-STAT pathway that have proven effective in the treatment of different immune-mediated diseases in adults and juvenile idiopathic arthritis (JIA). AIM OF STUDY: To evaluate the safety and efficacy of tofacitinib in children with different rheumatic diseases. MATERIAL AND

methodsWe extracted information from 24 children with the following diagnosis: JIA (

resultsCR was achieved in 10/24 patients; 7/15 among JIA patients, 1/2 among JDM patients, 4/7 among SAID patients, and PR in 5/15 of JIA, 1/2 of JDM, and 3/7 of SAID patients. Three non-responders with JIA discontinued tofacitinib. Corticosteroids were successfully tapered off in 11/14 patients and discontinued in 2/14 patients. Four patients had side effects not requiring treatment discontinuation: liver enzyme elevation (

conclusionJAK-inhibitors are effective new therapies for the treatment of multiple immune-mediated diseases. Our experience has shown the best results in patients with JIA and JIA-associated alopecia, and type I interferonopathies. More data from randomized controlled clinical trials are needed to use JAK-inhibitors safely in pediatric rheumatic diseases.

Indexed as

alopeciainterferonopathyinterferon type-IJAK-inhibitorsjuvenile dermatomyositisjuvenile idiopathic arthritistofacitinib

Identifiers

PMID35211430
PMCPMC8861449
OpenAlexW4210848455

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.