Evidence map›Paper›PMID 38231227›Full record

ReviewEuropean journal of clinical pharmacology2024

Tofacitinib for the treatment of severe rare skin diseases: a narrative review.

Fenglin Luo, Yuanyuan Zhang, Ping Wang

Abstract readReview
PubMed Publisher
In one paragraph

Review in European journal of clinical pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Fenglin LuoDepartment of Dermatology, Hangzhou Third People's Hospital, Hangzhou, 310000, China.ORCID http://orcid.org/0009-0003-1425-0895
Yuanyuan ZhangDepartment of Dermatology, Hangzhou Third People's Hospital, Hangzhou, 310000, China.ORCID http://orcid.org/0009-0000-1424-7774
Ping WangDepartment of Dermatology, Hangzhou Third People's Hospital, Hangzhou, 310000, China. dermwang@aliyun.com.ORCID http://orcid.org/0000-0002-6206-8073
Third People's Hospital of Hangzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAutoimmune bullous diseases, connective tissue diseases, and vasculitis represent a group of severe rare skin diseases. While glucocorticoids and immunosuppressive agents serve as standard treatments for these diseases, their efficacy is limited due to adverse side effects, indicating the need for alternative approaches. Biologics have been used in the management of some rare skin diseases. However, the use of biologics is associated with concerns, such as infection risk and high costs, prompting the quest for efficacious and cost-effective alternatives. This study discusses the safety issues associated with tofacitinib and its potential in treating rare skin diseases.

methodsThis narrative review focuses on the pharmacodynamic properties of tofacitinib and its impact on the JAK/STAT pathway. In addition, we present a comprehensive discussion of the effects and mechanism of action of tofacitinib for each severe rare skin disease.

resultsThis role of tofacitinib in treating severe rare skin diseases has been discussed, shedding light on its promising prospects as a treatment modality. Few reports of serious adverse events are available in patients treated with tofacitinib.

conclusionWe explored the mechanism of action, efficacy, and safety considerations of tofacitinib and found that it can be used as a treatment option for rare skin diseases. However, multicenter clinical studies are needed to confirm the efficacy and safety of JAK inhibitors.

Indexed as

Autoimmune DiseasesBiological ProductsPiperidinesPyrimidinesSkin DiseasesHumansJanus KinasesMulticenter Studies as TopicSignal TransductionSTAT Transcription FactorsBiological ProductsJanus KinasesPiperidinesPyrimidinesSTAT Transcription FactorstofacitinibAutoimmune bullous diseasesConnective tissue diseasesTofacitinibVasculitis

Identifiers

PMID38231227
OpenAlexW4390945579

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.