Evidence map›Paper›PMID 42124507›Full record

ArticleActa dermato-venereologica2026

Real-world Efficacy and Safety of Stapokibart in Children and Adolescents with Moderate-to-severe Atopic Dermatitis: A Retrospective Study.

Lubing Li, Yuqi Chen, Minmin Lin, Liyue Hou, Yijia Shao, Yihui Li, Junyi Shao, Xinhao Yu, Tongyao Chen, Zhiming Li

Abstract read
In one paragraph

Article in Acta dermato-venereologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Lubing LiDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.ORCID 0009-0004-7972-899X
Yuqi ChenDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Minmin LinDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Liyue HouDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Yijia ShaoDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Yihui LiDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Junyi ShaoDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xinhao YuDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Tongyao ChenDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Zhiming LiDepartment of Dermatology and Venereology, The first Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China. zhi-mingli@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paediatric real-world evidence for stapokibart in moderate-to-severe atopic dermatitis (AD) is scarce. We retrospectively analysed 55 patients aged 6-17 years treated at a single centre for 16 weeks using weight-tiered dosing (<30 kg: 600 mg loading, then 300 mg every 4 weeks; ≥30 kg: 600 mg loading, then 300 mg every 2 weeks). Eczema Area and Severity Index (EASI), Scoring Atopic Dermatitis (SCORAD), body surface area (BSA), Investigator's Global Assessment (IGA), Children's Dermatology Life Quality Index (CDLQI) and Pruritus Numerical Rating Scale (P-NRS) were assessed at baseline and weeks 4, 8, 12 and 16. At week 16, median EASI fell from 10.0 to 1.95 and SCORAD from 46.2 to 13.3; P-NRS from 8.0 to 1.0 and CDLQI from 14.0 to 4.0. Week 16 response rates were 92.7% (EASI-50), 70.9% (EASI-75), 38.2% (EASI-90), 52.7% (IGA 0/1) and 67.3% (P-NRS≤2). Mild adverse events occurred in 9.1%. Stapokibart was associated with rapid improvements in disease severity, itch and quality of life and was well tolerated in routine paediatric care.

Indexed as

Dermatitis, AtopicDermatologic AgentsAdolescentChildFemaleHumansMalePruritusQuality of LifeRetrospective StudiesSeverity of Illness IndexTime FactorsTreatment OutcomeDermatologic Agents

Identifiers

PMID42124507
PMCPMC13168788

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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.