Abrocitinib Monotherapy for Refractory Prurigo Nodularis: Report of Two Successful Cases

Prurigo nodularis (PN) is a debilitating chronic neuroimmunologic skin condition due to the intense pruritus and difficult to treat. The pruritogenic cytokines, particularly IL-4, IL-13, IL-22, IL-31, and oncostatin M (OSM), play a crucial role in the pathogenesis of PN, potentially involving the JAK1-STAT pathway. An oral JAK1 inhibitor, abrocitinib, is presently undergoing Phase 2 trials for the treatment of PN. We evaluated the efficacy of abrocitinib at a daily dosage of 100 mg in treating two patients with PN affecting both lower limbs: a 50-year-old male with a 16-year disease history and a 38-year-old female with over three years of disease history, both of whom had failed to respond to multiple conventional treatments. Both patients responded rapidly after one week of treatment and exhibited a marked improvement. Following eight weeks of therapy, near-complete resolution of both pruritus and lesions was achieved, and no adverse effects were reported. Additionally, there were no reported side effects during the initial four months of continued treatment. Abrocitinib is an effective targeted therapy for PN, offering a promising new option for refractory patients.

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Publication Details

Journal
Clinical Cosmetic and Investigational Dermatology
Published
2024-08-01
DOI
https://doi.org/10.2147/ccid.s470641
Citations
4
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
2.14
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article

Abrocitinib Monotherapy for Refractory Prurigo Nodularis: Report of Two Successful Cases

Xibao Zhang, Wenyan Liu, Jingyao Liang, Yihui Yu et al.
4 citations
Clinical Cosmetic and Investigational Dermatology
Dermatology and Skin Diseases
2.14
article

Abrocitinib Monotherapy for Refractory Prurigo Nodularis: Report of Two Successful Cases

Xibao Zhang, Wenyan Liu, Jingyao Liang, Yihui Yu, Hui Ye, Wei Li
article en
4 citations

Abstract

Prurigo nodularis (PN) is a debilitating chronic neuroimmunologic skin condition due to the intense pruritus and difficult to treat. The pruritogenic cytokines, particularly IL-4, IL-13, IL-22, IL-31, and oncostatin M (OSM), play a crucial role in the pathogenesis of PN, potentially involving the JAK1-STAT pathway. An oral JAK1 inhibitor, abrocitinib, is presently undergoing Phase 2 trials for the treatment of PN. We evaluated the efficacy of abrocitinib at a daily dosage of 100 mg in treating two patients with PN affecting both lower limbs: a 50-year-old male with a 16-year disease history and a 38-year-old female with over three years of disease history, both of whom had failed to respond to multiple conventional treatments. Both patients responded rapidly after one week of treatment and exhibited a marked improvement. Following eight weeks of therapy, near-complete resolution of both pruritus and lesions was achieved, and no adverse effects were reported. Additionally, there were no reported side effects during the initial four months of continued treatment. Abrocitinib is an effective targeted therapy for PN, offering a promising new option for refractory patients.

Clinical Cosmetic and Investigational DermatologyVol. Volume 17
Guangzhou Institute of Dermatology (CN), Guangzhou Medical University (CN)
Zero hunger
Openalex Percentile: Top 12%
Dermatology and Skin Diseases
2.14
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