Overview of use, efficacy, and safety of dupilumab in complex patients: a retrospective, case-series study from a large, urban academic center.


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 23 01 2022
accepted: 29 05 2022
revised: 05 04 2022
medline: 14 7 2023
pubmed: 19 6 2022
entrez: 18 6 2022
Statut: ppublish

Résumé

Dupilumab has emerged as an effective treatment option for those suffering from moderate-to-severe atopic dermatitis (AD). Since its approval in 2017 by the United States Food and Drug Administration, dupilumab demonstrated efficacy in a wide range of "off-label" dermatologic conditions. With its increasing use, dermatologists must navigate prescribing dupilumab in complex patient populations. To that end, we performed a single-institution, retrospective, case-series study to assess efficacy, tolerability, and safety of dupilumab in elderly, patients on concomitant immunosuppressive/immunomodulating therapies, and those with pre-existing co-morbidities (e.g., malignancies, chronic renal and/or liver diseases, organ transplantation, hematologic malignancies, and infection). We conducted chart reviews of 248 patients who were prescribed dupilumab between January 1, 2017 and August 31, 2021, and identified 64 patients who met the criteria of being in the complex patient group as described above. Our results showed that 87.5% (56/64) of complex patients demonstrated improvement and/or disease clearance on dupilumab. 20.3% (13/64) of them experienced one or more side effects reported as conjunctivitis, seborrheic dermatitis, psoriasiform eruption, xerosis, facial burning sensation, anaphylactic reaction/angioedema, and worsening of AD. 9.4% (6/64) of them discontinued dupilumab due to the side effects. These findings demonstrated that dupilumab can be safely considered in certain complex patient populations such as elderly and those with significant pre-existing co-morbidities and can be safely combined with immunosuppressive medications and/or other biologic therapies. In the future, more studies with long-term follow-up are needed to validate the efficacy and safety of dupilumab in these challenging patients with complex medical histories.

Identifiants

pubmed: 35716185
doi: 10.1007/s00403-022-02362-y
pii: 10.1007/s00403-022-02362-y
doi:

Substances chimiques

dupilumab 420K487FSG
Antibodies, Monoclonal, Humanized 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1777-1781

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Hendricks AJ, Yosipovitch G, Shi VY (2021) Dupilumab use in dermatologic conditions beyond atopic dermatitis - a systematic review. J Dermatol Treat 32(1):19–28. https://doi.org/10.1080/09546634.2019.1689227
doi: 10.1080/09546634.2019.1689227
Siliquini N, Giura MT, Viola R et al (2021) Atopic dermatitis, dupilumab and cancers: a case series. J Eur Acad Dermatol Venereol 35(10):e651–e652. https://doi.org/10.1111/jdv.17264
doi: 10.1111/jdv.17264 pubmed: 33797094
Patruno C, Napolitano M, Argenziano G et al (2021) Dupilumab therapy of atopic dermatitis of the elderly: a multicentre, real-life study. J Eur Acad Dermatol Venereol 35(4):958–964. https://doi.org/10.1111/jdv.17094
doi: 10.1111/jdv.17094 pubmed: 33332697
Ly K, Smith MP, Thibodeaux Q, Beck K, Bhutani T, Liao W (2019) Dupilumab in patients with chronic hepatitis B on concomitant entecavir. JAAD Case Rep 5(7):624–626. https://doi.org/10.1016/j.jdcr.2019.05.007
doi: 10.1016/j.jdcr.2019.05.007 pubmed: 31341942 pmcid: 6630033

Auteurs

Danitza Lukac (D)

Department of Dermatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.

Kyla Pagani (K)

Department of Dermatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.

Jean S McGee (JS)

Department of Dermatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA. jmcgee2@bidmc.harvard.edu.
Harvard Medical School, Boston, MA, USA. jmcgee2@bidmc.harvard.edu.

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Classifications MeSH