Evidence map›Paper›PMID 38018601›Full record

ArticleImmunity, inflammation and disease2023

Clinical effects of dupilumab: A novel treatment for Kimura disease.

Bing-Shiau Shang, Chang-Hung Hsiao, Teng-Fu Tsao, Yuan-Ya Liao, Wea-Lung Lin, Wen-I Lee, Ko-Huang Lue

Open access · goldAbstract readCase Reports
In one paragraph

Article in Immunity, inflammation and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Bing-Shiau ShangDepartment of Pediatrics, Chung Shan Medical University Hospital, Taichung City, Taiwan.
Chang-Hung HsiaoDepartment of Pediatrics, Cheng Ching Hospital, Taichung City, Taiwan.
Teng-Fu TsaoDepartment of Medicine, Chung Shan Medical University, Taichung City, Taiwan.
Yuan-Ya LiaoDepartment of Medicine, Chung Shan Medical University, Taichung City, Taiwan.
Wea-Lung LinDepartment of Pathology, Chung Shan Medical University Hospital, Taichung City, Taiwan.
Wen-I LeeDepartment of Pediatrics, Division of Allergy, Asthma, Immunology and Rheumatology, Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taoyuan, Taiwan.
Ko-Huang LueDepartment of Pediatrics, Chung Shan Medical University Hospital, Taichung City, Taiwan.ORCID 0000-0002-7573-5939
Chung Shan Medical University Hospital · TWChang Gung University · TWCheng Ching Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKimura disease (KD) is a rare chronic inflammatory disorder involving the Th2 pathway. Although medical treatment with steroids or other immunosuppressants is available, they may cause developmental issues in the pediatric population. Surgical intervention has also been suggested; however, it is associated with high recurrence rates. CASE PRESENTATION: A 14-year-old boy presented with left retroauricular lymph node enlargement at the age of 5 years. At the age of 7 years, he was diagnosed with nephrotic syndrome which subsided after steroid treatment for approximately 6 years. The retroauricular lymph node was surgically excised, and KD was confirmed. However, recurrent enlargement of the left retroauricular and neck lymph nodes occurred after 2 years. Persistently high IgE levels and fluctuating eosinophil counts were observed following steroid treatment. Dupilumab was prescribed because of the difficulty in tapering the steroid dosage. A loading dose of 600 mg was administered, followed by a maintenance dose of 300 mg every 2 weeks. The IgE level decreased after 3 months, and a low eosinophil count was maintained after steroid discontinuation. Follow-up computed tomography revealed a decrease in the size of the lymph nodes with no side effects such as conjunctivitis.

conclusionTraditional treatments have raised developmental concerns in the pediatric population and are associated with high recurrence rates. Dupilumab targets the Th2 pathway and provides effective results, with few adverse effects. Dupilumab may be a therapeutic option for KD and other diseases involving the Th2 pathway.

Indexed as

Angiolymphoid Hyperplasia with EosinophiliaKimura DiseaseAdolescentAntibodies, Monoclonal, HumanizedChildChild, PreschoolHumansImmunoglobulin EMaleSteroidsAntibodies, Monoclonal, HumanizeddupilumabImmunoglobulin ESteroidsdupilumabKimura diseasenephrotic syndromepediatric

Identifiers

PMID38018601
PMCPMC10632088
OpenAlexW4388510064

What OpenQuestion holds

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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.