Biologics in congenital ichthyosis: are they effective?


Journal

The British journal of dermatology
ISSN: 1365-2133
Titre abrégé: Br J Dermatol
Pays: England
ID NLM: 0004041

Informations de publication

Date de publication:
29 Oct 2024
Historique:
received: 26 07 2024
revised: 01 10 2024
accepted: 25 10 2024
medline: 29 10 2024
pubmed: 29 10 2024
entrez: 29 10 2024
Statut: aheadofprint

Résumé

Congenital ichthyoses (CI) comprise a heterogeneous group of genetic diseases requiring lifelong treatment and having a major effect on quality of life. Conventional treatments reduce scaling and skin discomfort; however, they usually have little or no effect on erythema and pruritus. The identification of cytokine alterations in CI raised the possibility of repurposing available biologics. Several case reports in the literature report successes using different biologics. We aimed to report the effects of biologics in real life. This was a retrospective, observational, international multicenter study of patients with CI treated with at least one biologic for a minimum of 3 months. The effect of the biologics was evaluated using an Investigator Global Assessment-Change (IGA-C) scale. A comprehensive literature search was performed in parallel. A total of 98 patients were included, with a mean age of 19.7 years and both sexes equally represented. Patients with Netherton syndrome (NS) or congenital ichthyosiform erythroderma (CIE) represented the majority of patients (30% and 21.4%, respectively). Most patients (84.7%) had a severe or very severe form of CI. The most frequently used biologics were inhibitors targeting interleukin-17 (IL-17), IL-12/IL-23, or the IL-4 receptor. The mean duration of treatment was 22+20.1 months. There were 45 responders (45.9%), including 18 patients (18.3%) who were good responders; all had an erythrodermic CI subset and received one of the three main biologics. In 2 NS and CIE, IL-12/IL-23 and IL-4 receptor inhibitors tended to be most effective. Review of the literature revealed a shorter mean duration of use of biologics (11.5+8.5 months) and higher percentage of responders (85.7%), suggesting reporter bias. This series identified subsets of CI that may respond to biologics and will aid in designing future clinical trials of biologics for CI.

Sections du résumé

BACKGROUND BACKGROUND
Congenital ichthyoses (CI) comprise a heterogeneous group of genetic diseases requiring lifelong treatment and having a major effect on quality of life. Conventional treatments reduce scaling and skin discomfort; however, they usually have little or no effect on erythema and pruritus. The identification of cytokine alterations in CI raised the possibility of repurposing available biologics. Several case reports in the literature report successes using different biologics.
OBJECTIVE OBJECTIVE
We aimed to report the effects of biologics in real life.
METHODS METHODS
This was a retrospective, observational, international multicenter study of patients with CI treated with at least one biologic for a minimum of 3 months. The effect of the biologics was evaluated using an Investigator Global Assessment-Change (IGA-C) scale. A comprehensive literature search was performed in parallel.
RESULTS RESULTS
A total of 98 patients were included, with a mean age of 19.7 years and both sexes equally represented. Patients with Netherton syndrome (NS) or congenital ichthyosiform erythroderma (CIE) represented the majority of patients (30% and 21.4%, respectively). Most patients (84.7%) had a severe or very severe form of CI. The most frequently used biologics were inhibitors targeting interleukin-17 (IL-17), IL-12/IL-23, or the IL-4 receptor. The mean duration of treatment was 22+20.1 months. There were 45 responders (45.9%), including 18 patients (18.3%) who were good responders; all had an erythrodermic CI subset and received one of the three main biologics. In 2 NS and CIE, IL-12/IL-23 and IL-4 receptor inhibitors tended to be most effective. Review of the literature revealed a shorter mean duration of use of biologics (11.5+8.5 months) and higher percentage of responders (85.7%), suggesting reporter bias.
CONCLUSION CONCLUSIONS
This series identified subsets of CI that may respond to biologics and will aid in designing future clinical trials of biologics for CI.

Identifiants

pubmed: 39470394
pii: 7848640
doi: 10.1093/bjd/ljae420
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of British Association of Dermatologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Juliette Mazereeuw-Hautier (J)

Department of Dermatology, Reference Centre for Rare Skin Diseases, CHU de Toulouse, University Paul Sabatier, Toulouse, France.

Céline Granier Tournier (C)

Department of Dermatology, Reference Centre for Rare Skin Diseases, CHU de Toulouse, University Paul Sabatier, Toulouse, France.

Angela Hernandez-Martin (A)

Department of Dermatology, Hospital Infantil Niño Jesús, Madrid, Spain.

Sarah Milesi (S)

Department of Dermatology, Reference Centre for Rare Skin Diseases, CHU de Toulouse, University Paul Sabatier, Toulouse, France.

Hélène Texier (H)

Department of Dermatology, Reference Centre for Rare Skin Diseases, CHU de Toulouse, University Paul Sabatier, Toulouse, France.

Maëlla Severino-Freire (M)

Department of Dermatology, Reference Centre for Rare Skin Diseases, CHU de Toulouse, University Paul Sabatier, Toulouse, France.

Nathalia Bellon (N)

Department of Dermatology, Necker Enfants Malades Hospital APHP, Expert Center for Genodermatoses MAGEC-Necker, Paris, France.

Christine Bodemer (C)

Department of Dermatology, Necker Enfants Malades Hospital APHP, Expert Center for Genodermatoses MAGEC-Necker, Paris, France.
Université Paris Cité, Paris, France.
ERN-Skin (ern-skin.eu).

Robert Gruber (R)

Department of Dermatology, Venereology and Allergy, Medical University of Innsbruck, Innsbruck, Austria.

Emmanuel Mahé (E)

Department of Dermatology, Centre Hospitalier Victor Dupouy d'Argenteuil, Argenteuil, France.

Fanny Morice Picard (F)

Department of Dermatology, CHU de Bordeaux, Paris, France.

Katariina Hannula-Jouppi (K)

Department of Dermatology and Allergology, ERN-Skin center, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.

Jenny E Murase (JE)

Department of Dermatology, University of California, San Francisco, USA.
Department of Dermatology, Palo Alto Foundation Medical Group, Mountain View, California.

Sébastien Barbarot (S)

Department of Dermatology, Nantes Université, CHU Nantes, INRAE, UMR 1280, PhAN, Nantes, France.

Eran Cohen-Barak (E)

Department of Dermatology, Emek Medical Center, Rappaport Faculty of Medicine, Technion, Israel.

Maurico Torres-Pradilla (M)

Department of Dermatology, Hospital de San Jose, Fundacion Universitaria de Ciencias de la Salud, Bogota Colombia.

Anna Bruckner (A)

University of Colorado School of Medicine, Aurora, Colorado, USA.

Moise Levy (M)

Department of Pediatrics, University of Texas at Austin, Dell medical school, Houston, USA.

Mark J A Koh (MJA)

Department of Dermatology, KK Women's & Children's Hospital, Singapore.

Marie Masson Regnault (M)

Department of Dermatology, Polyclinique Francheville, Périgueux, France.

Vanya Rossel (V)

Department of Dermatology, Maastricht University, Medical Center, Maastricht, Netherland.

Christine Chiaverini (C)

Department of Dermatology, CHU de Nice, Nice, France.

Lisa M Arkin (LM)

University of Wisconsin-Madison, USA.

Hagen Ott (H)

Department of of Pediatric Dermatology and Allergology Children`s Hospital Auf Der Bult, Germany.

Cristina Has (C)

Department of Dermatology and Venereology, Medical Center-University of Freiburg, Germany.

Kira Süβmuth (K)

Department of Dermatology and Allergology, Helios Klinikum Berlin-Buch, Campus of Medical School Berlin, Berlin, Germany.

Antoni Gostynski (A)

Department of Dermatology, Maastricht University, Medical Center, Maastricht, Netherland.

Jason Shourick (J)

Department of Epidemiology, CHU Toulouse, Faculté de médecine de Purpan, Toulouse, France.

Amy S Paller (AS)

Departments of Dermatology and Pediatrics, Northwestern, University Feinberg School of Medicine, Chicago, Illinois, USA.

Classifications MeSH