Journal article

Effectiveness, biomarker transition, and safety of 48-week tralokinumab treatment for atopic dermatitis: real-world analyses stratified by age groups (15-17, 18-64, and ≥ 65 years)

Pages 156 to 165

Cite this article


  • Takahashi, Y.,
  • Hagino, T.,
  • Uchiyama, A.,
  • Saeki, H.,
  • Fujimoto, E.,
  • Motegi, S.-i.
  • and Kanda, N.
(2026). Effectiveness, Biomarker Transition, And Safety of 48-Week Tralokinumab Treatment for Atopic Dermatitis: Real-World Analyses Stratified by Age Groups (15-17, 18-64, And ≥ 65 Years) European Journal of Dermatology, . 36(2), 156-165. https://doi.org/10.1684/ejd.2026.5060.

  • Takahashi, Yohei.,
  • et al.
« Effectiveness, biomarker transition, and safety of 48-week tralokinumab treatment for atopic dermatitis: real-world analyses stratified by age groups (15-17, 18-64, and ≥ 65 years) ». European Journal of Dermatology, 2026/2 Vol. 36, 2026. p.156-165. CAIRN.INFO, stm.cairn.info/revue-european-journal-of-dermatology-2026-2-page-156?lang=en.

  • TAKAHASHI, Yohei,
  • HAGINO, Teppei,
  • UCHIYAMA, Akihiko,
  • SAEKI, Hidehisa,
  • FUJIMOTO, Eita,
  • MOTEGI, Sei-ichiro
  • and KANDA, Naoko,
2026. Effectiveness, biomarker transition, and safety of 48-week tralokinumab treatment for atopic dermatitis: real-world analyses stratified by age groups (15-17, 18-64, and ≥ 65 years) European Journal of Dermatology, 2026/2 Vol. 36, p.156-165. DOI : 10.1684/ejd.2026.5060. URL : https://stm.cairn.info/revue-european-journal-of-dermatology-2026-2-page-156?lang=en.

https://doi.org/10.1684/ejd.2026.5060


English

Background
Tralokinumab, an anti-interleukin-13 monoclonal antibody, is effective for atopic dermatitis (AD). However, long-term (one-year) clinical outcomes stratified by age groups have not been sufficiently studied.
Objectives
To evaluate the effectiveness of 48-week tralokinumab treatment for patients with AD, stratified by age groups (15-17, 18-64, and ≥65 years).
Materials & Methods
We conducted a prospective study from October 2023 to May 2025 in 194 Japanese patients aged ≥15 years with moderate-to-severe AD. Patients received tralokinumab every two weeks for 48 weeks. Outcomes included transitions in total EASI, anatomical site-specific EASI, PP-NRS, and IGA, achievement rates of EASI50/75/90/100, IGA0/1, and PP-NRS4, transitions of blood biomarkers (total IgE, TARC, LDH, and TEC), and treatment-emergent adverse events.
Results
Mean scores of total and anatomical site-specific EASI and PP-NRS decreased similarly across all age groups through week 48. At week 48, the achievement rates of EASI 75 and PP-NRS 4 were 87.5% and 66.7% in patients aged 15-17 years, 92.5% and 63.1% in those aged 18-64 years, and 81.8% and 66.7% in those aged ≥65 years (p>0.05), respectively.
Conclusion
Tralokinumab reduced both EASI and PP-NRS scores throughout 48 weeks in patients with AD across all age groups. These findings suggest that tralokinumab may be effective in a wide range of patients, from adolescents to the elderly.

keywords

  • atopic dermatitis
  • tralokinumab
  • interleukin-13
  • adole­scent
  • elderly

Publisher keywords: atopic dermatitis, tralokinumab, interleukin-13, adole­scent, elderly

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