Evidence map›Paper›PMID 36593080›Full record

ArticleRMD open2023

Efficacy and safety of dose escalation of tofacitinib in refractory anti-MDA5 antibody-positive dermatomyositis.

Tomoaki Ida, Shunsuke Furuta, Asuka Takayama, Jun Tamura, Yuki Hayashi, Kazuya Abe, Syunjiro Kurihara, Junichi Ishikawa, Taro Iwamoto, Kei Ikeda and 2 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
10.9field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  16. Treating connective tissue disease-associated interstitial lung disease - think outside the box: a perspective.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  17. Review
  18. Article
  19. Review
  20. Effectiveness and safety of tofacitinibThe European respiratory journal · 2025
    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

12 authors at 1 institution in 1 country.

Tomoaki IdaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.ORCID 0000-0002-8023-336X
Shunsuke FurutaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan shfuruta@chiba-u.jp.
Asuka TakayamaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Jun TamuraDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Yuki HayashiDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Kazuya AbeDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Syunjiro KuriharaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Junichi IshikawaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.
Taro IwamotoDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.ORCID 0000-0003-1663-3518
Kei IkedaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.ORCID 0000-0003-0574-9611
Kotaro SuzukiDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.ORCID 0000-0002-4692-2970
Hiroshi NakajimaDepartment of Allergy and Clinical Immunology, Chiba University, Chiba, Chiba, Japan.ORCID 0000-0001-8595-9381
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-melanoma differentiation-associated protein 5 (MDA5) antibody-positive dermatomyositis (MDA5-DM) is frequently complicated with rapidly progressive-interstitial lung disease (RP-ILD). The prognosis of MDA5-DM with RP-ILD is mostly poor despite intensive treatment with a combination of high-dose glucocorticoids and single conventional immunosuppressants. It was reported that the triple therapy (high-dose glucocorticoids, cyclophosphamide and tacrolimus) was more effective than a combination of high-dose glucocorticoids and stepwise addition of immunosuppressants. In addition, the efficacy of tofacitinib 10 mg/day for MDA5-DM with RP-ILD refractory to the triple therapy was suggested. However, the effect of those therapies was evaluated only in comparison to the historical control. Moreover, more importantly, there are still refractory patients even if treated with those therapies. In this case series, we report six MDA5-DM cases with RP-ILD in which the dose of tofacitinib was increased from 10 mg to 20 mg/day due to poor response to the triple therapy, followed by tofacitinib 10 mg/day. Four of six patients improved after dose escalation of tofacitinib, while two non-responders died. All six patients developed at least one infection including five cases of cytomegalovirus reactivation, one pulmonary aspergillosis, one herpes zoster and one herpes simplex keratitis. These cases suggest that the dose escalation of tofacitinib can be an option for MDA5-DM patients refractory to 10 mg/day of tofacitinib and other immunosuppressants although the risk of infection is a concern. The risk-benefit balance of the dose escalation of tofacitinib should be carefully assessed in each case.

Indexed as

DermatomyositisImmunosuppressive AgentsGlucocorticoidsHumansLung Diseases, InterstitialPiperidinesPyrimidinesGlucocorticoidsImmunosuppressive AgentsPiperidinesPyrimidinestofacitinibCytokinesDermatomyositisTherapeutics

Identifiers

PMID36593080
PMCPMC9809321
OpenAlexW4313406819

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.