Dupilumab improves clinical manifestations, symptoms, and quality of life in adult patients with chronic nodular prurigo.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 09 10 2019
revised: 18 02 2020
accepted: 18 03 2020
pubmed: 2 4 2020
medline: 20 1 2021
entrez: 2 4 2020
Statut: ppublish

Résumé

Chronic nodular prurigo (CNPG) is a multifactorial skin disease characterized by itchy papules and nodules, usually resistant to standard treatment and associated with markedly impaired quality of life. To describe dupilumab effectiveness and tolerability in treating adult patients with CNPG refractory to both topical and systemic therapies. Retrospective, multicenter study including adult patients affected by CNPG, who were treated with dupilumab for at least 16 weeks. Twenty-seven CNPG patients showed clinical improvement in terms of skin lesions, itch, sleeplessness, and quality of life. A consistent proportion of patients (24/27; 88.9%) had at least 16-week continuous treatment and achieved Investigator Global Assessment score 1 (11/24; 45.8%). An increased number of patients achieved at least a 2-grade reduction in Investigator Global Assessment score (19/24; 79.2%). Numeric rating scale values for itch and sleeplessness decreased from 8.9 to 2.7 and from 8.2 to 1.7, respectively (P < .001) after 16-week therapy. Ten patients achieved 36 weeks of continuous treatment while maintaining clinical efficacy. Major limitations included lack of validated assessment tools at the initial data collection, a limited cohort of treated patients, and a short-term observation period. Dupilumab was proven effective in reducing itch and improving CNPG skin lesions.

Sections du résumé

BACKGROUND BACKGROUND
Chronic nodular prurigo (CNPG) is a multifactorial skin disease characterized by itchy papules and nodules, usually resistant to standard treatment and associated with markedly impaired quality of life.
OBJECTIVE OBJECTIVE
To describe dupilumab effectiveness and tolerability in treating adult patients with CNPG refractory to both topical and systemic therapies.
METHODS METHODS
Retrospective, multicenter study including adult patients affected by CNPG, who were treated with dupilumab for at least 16 weeks.
RESULTS RESULTS
Twenty-seven CNPG patients showed clinical improvement in terms of skin lesions, itch, sleeplessness, and quality of life. A consistent proportion of patients (24/27; 88.9%) had at least 16-week continuous treatment and achieved Investigator Global Assessment score 1 (11/24; 45.8%). An increased number of patients achieved at least a 2-grade reduction in Investigator Global Assessment score (19/24; 79.2%). Numeric rating scale values for itch and sleeplessness decreased from 8.9 to 2.7 and from 8.2 to 1.7, respectively (P < .001) after 16-week therapy. Ten patients achieved 36 weeks of continuous treatment while maintaining clinical efficacy.
LIMITATIONS CONCLUSIONS
Major limitations included lack of validated assessment tools at the initial data collection, a limited cohort of treated patients, and a short-term observation period.
CONCLUSION CONCLUSIONS
Dupilumab was proven effective in reducing itch and improving CNPG skin lesions.

Identifiants

pubmed: 32229281
pii: S0190-9622(20)30469-2
doi: 10.1016/j.jaad.2020.03.049
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Dermatologic Agents 0
Interleukin-4 Receptor alpha Subunit 0
dupilumab 420K487FSG

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-45

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Andrea Chiricozzi (A)

Institute of Dermatology, Catholic University, Rome, Italy; Dermatology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy. Electronic address: chiricozziandrea@gmail.com.

Martina Maurelli (M)

Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy.

Niccolò Gori (N)

Institute of Dermatology, Catholic University, Rome, Italy.

Giuseppe Argenziano (G)

Dermatology Unit, Department of Mental and Physical Health and Preventive Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.

Clara De Simone (C)

Institute of Dermatology, Catholic University, Rome, Italy; Dermatology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Giulia Calabrese (G)

Dermatology Unit, Department of Mental and Physical Health and Preventive Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.

Giampiero Girolomoni (G)

Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy.

Ketty Peris (K)

Institute of Dermatology, Catholic University, Rome, Italy; Dermatology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

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Classifications MeSH