Tumor necrosis factor-α inhibitor-induced psoriasis: Systematic review of clinical features, histopathological findings, and management experience

Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Systematic review of published cases of TNF-α inhibitor-induced psoriasis. We identified 88 a...

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Published inJournal of the American Academy of Dermatology Vol. 76; no. 2; pp. 334 - 341
Main Authors Brown, Gabrielle, Wang, Eva, Leon, Argentina, Huynh, Monica, Wehner, Mackenzie, Matro, Rebecca, Linos, Eleni, Liao, Wilson, Haemel, Anna
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2017
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Online AccessGet full text
ISSN0190-9622
1097-6787
DOI10.1016/j.jaad.2016.08.012

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Abstract Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Systematic review of published cases of TNF-α inhibitor-induced psoriasis. We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%). Retrospective review that relies on case reports and series. While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases.
AbstractList Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Systematic review of published cases of TNF-α inhibitor-induced psoriasis. We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%). Retrospective review that relies on case reports and series. While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases.
Background Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. Objective To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Methods Systematic review of published cases of TNF-α inhibitor-induced psoriasis. Results We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%). Limitations Retrospective review that relies on case reports and series. Conclusion While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases.
Author Leon, Argentina
Brown, Gabrielle
Liao, Wilson
Matro, Rebecca
Wang, Eva
Wehner, Mackenzie
Haemel, Anna
Linos, Eleni
Huynh, Monica
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  surname: Brown
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  organization: Department of Dermatology, University of California, San Francisco, California
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  surname: Wang
  fullname: Wang, Eva
  organization: Department of Dermatology, University of California, San Francisco, California
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  givenname: Argentina
  surname: Leon
  fullname: Leon, Argentina
  organization: Department of Dermatology, University of California, San Francisco, California
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  givenname: Monica
  surname: Huynh
  fullname: Huynh, Monica
  organization: Department of Dermatology, University of California, San Francisco, California
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  givenname: Mackenzie
  surname: Wehner
  fullname: Wehner, Mackenzie
  organization: Department of Dermatology, University of California, San Francisco, California
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  givenname: Rebecca
  surname: Matro
  fullname: Matro, Rebecca
  organization: Department of Gastroenterology, University of California, San Francisco, California
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  surname: Linos
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  surname: Liao
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  givenname: Anna
  surname: Haemel
  fullname: Haemel, Anna
  email: Anna.Haemel@ucsf.edu
  organization: Department of Dermatology, University of California, San Francisco, California
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Issue 2
Keywords medication side effect
CD
IL
etanercept
infliximab
AZA
adverse event
certolizumab
MeSH
tumor necrosis factor-α inhibitor
adalimumab
golimumab
UC
RA
IFN-α
MTX
AS
IL-23R
TH
TNF-α
tumor necrosis factor-α-induced psoriasis
psoriasis
ankylosing spondylitis
methotrexate
interleukin-23 receptor
interferon α
ulcerative colitis
interleukin
T helper
azathioprine
rheumatoid arthritis
medical subject headings
Crohn disease
tumor necrosis factor-α
T H
Language English
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Snippet Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. To better define the demographic, clinical features, and treatment...
Background Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. Objective To better define the demographic, clinical...
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SubjectTerms adalimumab
Adolescent
Adult
adverse event
Aged
Aged, 80 and over
certolizumab
Child
Dermatology
Drug Eruptions - diagnosis
Drug Eruptions - etiology
Drug Eruptions - therapy
etanercept
Female
golimumab
Humans
infliximab
Male
medication side effect
Middle Aged
psoriasis
Psoriasis - chemically induced
Psoriasis - diagnosis
Psoriasis - therapy
Tumor Necrosis Factor-alpha - antagonists & inhibitors
tumor necrosis factor-α inhibitor
tumor necrosis factor-α-induced psoriasis
Young Adult
Title Tumor necrosis factor-α inhibitor-induced psoriasis: Systematic review of clinical features, histopathological findings, and management experience
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0190962216306314
https://www.clinicalkey.es/playcontent/1-s2.0-S0190962216306314
https://dx.doi.org/10.1016/j.jaad.2016.08.012
https://www.ncbi.nlm.nih.gov/pubmed/27720274
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