Skip to main navigation Skip to search Skip to main content

Efficacy and safety of JAK inhibitors in patients aged > 60 years with moderate-to-severe atopic dermatitis: a 52-week multicenter, real-life study—IL AD (Italian Landscape Atopic Dermatitis)

  • Luca Potestio
  • , Cataldo Patruno
  • , Alessandra Narcisi
  • , Antonio Costanzo
  • , Luciano Ibba
  • , Luigi Gargiulo
  • , Piergiorgio Malagoli
  • , Michela Ortoncelli
  • , Simone Ribero
  • , Luca Mastorino
  • , Francesco Leo
  • , Silvia Mariel Ferrucci
  • , Luisa Angileri
  • , Francesca Barei
  • , Luca Stingeni
  • , Katharina Hansel
  • , Claudio Sciarrone
  • , Giampiero Girolomoni
  • , Martina Maurelli
  • , Caterina Foti
  • Benedetta Tirone, Anna Balato, Maria Esposito, Giovanni Paolino, Santo Raffaele Mercuri, Elena Pezzolo, Paola Savoia, Claudio Brescia, Maddalena Napolitano

Research output: Contribution to journalArticlepeer-review

Abstract

Atopic dermatitis (AD) prevalence in elderly patients is increasing. Clinically, elderly AD may present with atypical phenotypes, making the diagnosis difficult. Moreover, treatment challenges arise due to treatment-resistance, comorbidities, polypharmacy, and contraindications to existing therapies. Janus kinase (JAK) inhibitors (abrocitinib, baricitinib, upadacitinib) may offer a valuable alternative. However, their use in elderly populations remains unclear, as older patients are often excluded from clinical trials, and several concerns have been raised about their safety in this category of subjects. This study aimed to evaluate the efficacy and safety of JAK inhibitors in elderly patients with moderate-to-severe AD. A 52-week, multicenter, real-life study was performed enrolling patients aged ≥ 60 years affected by moderate-to-severe AD undergoing treatment with JAK inhibitors for at least 16 weeks across 16 dermatological centers in Italy. Disease severity was assessed at baseline, week (W) 4, 16, 24, and 52 using the Eczema Area and Severity Index (EASI), Dermatology Life Quality Index (DLQI), and Pruritus-Numerical Rating Scale (P-NRS). Adverse events (AEs) were recorded at each follow-up. A total of 72 patients met the inclusion criteria [abrocitinib: 13 (18.06%); baricitinib: 6 (8.33%); upadacitinib: 53 (73.61%)]. Of these, 72 (100.0%) achieved W16 follow-up with 33 (45.83%) and 26 (36.11%) subjects reaching W24 and W52, respectively. At baseline, mean EASI, DLQI and P-NRS were 21.22 ± 10.38, 18.21 ± 7.33, and 7.84 ± 1.94, respectively. A significant improvement in all scores was observed starting from W4 [EASI: 4.77 ± 5.07, DLQI: 4.01 ± 3.98, P-NRS: 1.66 ± 1.83 (p < 0.0001 for all)], continuing to improve up to W52 [EASI: 0.81 ± 1.27, DLQI: 0.31 ± 0.63, P-NRS: 0.42 ± 1.03; (p < 0.0001 for all)]. No treatment interruptions or modifications for ineffectiveness or AEs were registered. No statistically significant differences in terms of efficacy and safety were found among the treatment groups. JAK inhibitors demonstrated significant efficacy and an acceptable safety profile in elderly AD patients.

Original languageEnglish
Article number777
JournalArchives of Dermatological Research
Volume317
Issue number1
DOIs
Publication statusPublished - Dec 2025

Keywords

  • Abrocitinib
  • Atopic dermatitis
  • Baricitinib
  • Elderly patients
  • JAK inhibitors
  • Management
  • Upadacitinib

Fingerprint

Dive into the research topics of 'Efficacy and safety of JAK inhibitors in patients aged > 60 years with moderate-to-severe atopic dermatitis: a 52-week multicenter, real-life study—IL AD (Italian Landscape Atopic Dermatitis)'. Together they form a unique fingerprint.

Cite this