Biologic treatment outcomes in mucous membrane pemphigoid: A systematic review.


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:
07 2022
Historique:
received: 31 08 2020
revised: 24 11 2020
accepted: 19 12 2020
pubmed: 11 1 2021
medline: 22 6 2022
entrez: 10 1 2021
Statut: ppublish

Résumé

Mucous membrane pemphigoid (MMP) is an autoimmune disease that can lead to fibrosis of mucous membranes and functional impairment. Biologic agents should be explored as alternative treatment options to improve outcomes. To conduct a systematic review of biologic treatment outcomes in patients with MMP. A MEDLINE and Embase search was conducted on July 23, 2020, to include 63 studies using Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines. Use of intravenous immunoglobulin (n = 154), rituximab (n = 112), tumor necrosis factor α inhibitors (n = 7), and combination treatments (n = 58) were reported in 331 patients with MMP. Intravenous immunoglobulin led to complete resolution in 61.7% (n = 95/154) of patients within 26.0 months, with a recurrence rate of 22.7% (n = 35/154) and headache as the most common adverse effect (8.4%, n = 13/154). Rituximab led to complete resolution in 70.5% (n = 79/112) of patients within 8.7 months, with a recurrence rate of 35.7% (n = 40/112). The most commonly reported adverse effects were urinary tract infections (4.5%, n = 5/112), leukocytopenia (2.7%, n = 3/112), and death due to severe infections (1.8%, n = 2/112). Tumor necrosis factor α inhibitors led to complete resolution in 71.4% (n = 5/7) of patients within 3.9 months of treatment without reported adverse events. Randomized clinical trials with long-term follow-up are required to conclude the promising safety and efficacy of biologic agents in patients with MMP.

Sections du résumé

BACKGROUND
Mucous membrane pemphigoid (MMP) is an autoimmune disease that can lead to fibrosis of mucous membranes and functional impairment. Biologic agents should be explored as alternative treatment options to improve outcomes.
OBJECTIVE
To conduct a systematic review of biologic treatment outcomes in patients with MMP.
METHODS
A MEDLINE and Embase search was conducted on July 23, 2020, to include 63 studies using Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines.
RESULTS
Use of intravenous immunoglobulin (n = 154), rituximab (n = 112), tumor necrosis factor α inhibitors (n = 7), and combination treatments (n = 58) were reported in 331 patients with MMP. Intravenous immunoglobulin led to complete resolution in 61.7% (n = 95/154) of patients within 26.0 months, with a recurrence rate of 22.7% (n = 35/154) and headache as the most common adverse effect (8.4%, n = 13/154). Rituximab led to complete resolution in 70.5% (n = 79/112) of patients within 8.7 months, with a recurrence rate of 35.7% (n = 40/112). The most commonly reported adverse effects were urinary tract infections (4.5%, n = 5/112), leukocytopenia (2.7%, n = 3/112), and death due to severe infections (1.8%, n = 2/112). Tumor necrosis factor α inhibitors led to complete resolution in 71.4% (n = 5/7) of patients within 3.9 months of treatment without reported adverse events.
CONCLUSIONS
Randomized clinical trials with long-term follow-up are required to conclude the promising safety and efficacy of biologic agents in patients with MMP.

Identifiants

pubmed: 33422625
pii: S0190-9622(21)00010-4
doi: 10.1016/j.jaad.2020.12.056
pii:
doi:

Substances chimiques

Biological Products 0
Immunoglobulins, Intravenous 0
Immunosuppressive Agents 0
Rituximab 4F4X42SYQ6
Tumor Necrosis Factor Inhibitors 0

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

110-120

Informations de copyright

Copyright © 2021 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest Dr Yeung has been a speaker, consultant, and investigator for AbbVie, Allergan, Amgen, Astellas, Boehringer Ingelheim, Celgene, Centocor, Coherus, Dermira, Eli Lilly, Forward, Galderma, GSK, Janssen, Leo, Medimmune, Merck, Novartis, Pfizer, Regeneron, Roche, Sanofi Genzyme, Takeda, UCB, Valeant, and Xenon. Dr Lytvyn, Author Rahat, Dr Mufti, and Authors Witol, Bagit, and Sachdeva have no conflicts of interest to declare.

Auteurs

Yuliya Lytvyn (Y)

Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Shahmina Rahat (S)

Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.

Asfandyar Mufti (A)

Division of Dermatology, Department of Medicine, University of Toronto, Toronto, ON, Canada.

Adrian Witol (A)

Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Ahmed Bagit (A)

Faculty of Health Sciences, Brock University, St. Catharines, ON, Canada.

Muskaan Sachdeva (M)

Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Jensen Yeung (J)

Division of Dermatology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Sunnybrook Health Sciences Centre, Toronto, ON, Canada; Division of Dermatology, Women's College Hospital, Toronto, ON, Canada. Electronic address: jensen.yeung@utoronto.ca.

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Classifications MeSH