Evidence map›Paper›PMID 41489176›Full record

ArticleThe Journal of dermatology2026

Long-Term, Site-Specific Effectiveness of Tralokinumab in Atopic Dermatitis: A 72-Week Real-World Study.

Mizuki Shiba, Teppei Hagino, Akihiko Uchiyama, Hidehisa Saeki, Eita Fujimoto, Sei-Ichiro Motegi, Naoko Kanda

Abstract readMulticenter Study
In one paragraph

Article in The Journal of dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Mizuki ShibaDepartment of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.
Teppei HaginoDepartment of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.ORCID https://orcid.org/0000-0002-4183-9596
Akihiko UchiyamaDepartment of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan.ORCID https://orcid.org/0000-0002-2169-2427
Hidehisa SaekiDepartment of Dermatology, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1095-0355
Eita FujimotoDepartment of Dermatology, Fujimoto Dermatology Clinic, Funabashi, Japan.ORCID https://orcid.org/0009-0002-5914-3244
Sei-Ichiro MotegiDepartment of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan.ORCID https://orcid.org/0000-0001-8286-0669
Naoko KandaDepartment of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.ORCID https://orcid.org/0000-0003-4389-2312

Funding

Maruho Takagi Dermatology FoundationTorii Pharmaceutical
6 · The paper itself

Abstract

Tralokinumab, an anti-IL-13 antibody, is effective for atopic dermatitis (AD); however, its long-term (> 1 year) effectiveness specific to each anatomical site is unknown in real-world settings. To evaluate 72-week effectiveness of tralokinumab on different anatomical sites in AD, we studied 208 patients with moderate-to-severe AD treated with tralokinumab for 72 weeks. Eczema area and severity index (EASI) scores were analyzed on four anatomical sites (head/neck, trunk, upper limbs, and lower limbs). Tralokinumab consistently reduced EASI on all anatomical sites. The achievement rates of EASI 75 and 100 on each site gradually increased from Week 4 to Week 72, and those on lower limbs appeared higher compared to the other sites. The percent reductions of EASI throughout 72 weeks appeared slightly lower on head and neck compared to the other sites. Week 72 achievement rate of EASI 75 on head/neck, trunk, upper limbs, or lower limbs was 80.4%, 80%, 80.3%, or 86.7%, while that of EASI 100 was 37.3%, 25.0%, 27.4%, and 40.0%, respectively. Tralokinumab reduced EASI scores through 72 weeks across different anatomical sites in AD patients. The achievement rates of EASI 75 and 100 appeared slightly higher on lower limbs compared to the other sites.

Indexed as

Antibodies, MonoclonalDermatitis, AtopicDermatologic AgentsAdolescentAdultFemaleHeadHumansInterleukin-13Lower ExtremityMaleMiddle AgedNeckSeverity of Illness IndexTime FactorsTorsoAntibodies, MonoclonalDermatologic AgentsInterleukin-13tralokinumabatopic dermatitisinterleukin‐13real‐worldsite‐specifictralokinumab

Identifiers

PMID41489176
PMCPMC12967683

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.