Dupilumab ocular side effects in patients with atopic dermatitis : a systematic review
© 2022 European Academy of Dermatology and Venereology..
Atopic dermatitis (AD) is a chronic, inflammatory skin disorder that most frequently occurs in children, but it can also affect adults. Even though most AD cases can be managed with topical treatments, moderate-to-severe forms require systemic therapies. Dupilumab is the first human monoclonal antibody approved for the treatment of AD. Its action is through IL-4 receptor alpha subunit inhibition, thus blocking IL-4 and IL-13 signaling pathways. It has been shown to be an effective, well-tolerated therapy for AD, as well as for asthma, chronic rhinosinusitis with nasal polyposis (CRSwNP), and eosinophilic esophagitis (EoE). However, an increasing incidence of dupilumab-induced ocular surface disease (DIOSD) has been reported in patients treated with dupilumab, as compared to placebo. The aim of this study was to summarize scientific data regarding DIOSD in AD patients treated with dupilumab. A search of PubMed and clinicaltrials.gov databases was performed. There was no limit to study design. All AD cases were moderate-to-severe. DIOSD was either dermatologist-, allergist-, or ophthalmologist-assessed. Evidence shows that DIOSD occurs most frequently in patients with atopic dermatitis and not in other skin conditions, neither in patients with asthma, CRSwNP, nor EoE who are on dupilumab treatment. Further studies are warranted in order to establish a causal relationship between dupilumab and ocular surface disease. Nevertheless, ophthalmological evaluations prior to dupilumab initiation can benefit AD patients with previous ocular pathology or current ocular symptomatology. Also, patch testing for ocular allergic contact dermatitis might be advantageous in patients with a history of allergic conjunctivitis. Furthermore, TARC, IgE, and circulating eosinophils levels might be important biomarkers for a baseline assessment of future candidates to dupilumab treatment. However, TARC measurements should be resumed for research purposes only.
Errataetall: |
CommentIn: J Eur Acad Dermatol Venereol. 2022 Dec;36(12):e988-e989. - PMID 35790032 |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:36 |
---|---|
Enthalten in: |
Journal of the European Academy of Dermatology and Venereology : JEADV - 36(2022), 6 vom: 15. Juni, Seite 820-835 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Neagu, N [VerfasserIn] |
---|
Links: |
---|
Themen: |
420K487FSG |
---|
Anmerkungen: |
Date Completed 12.05.2022 Date Revised 15.11.2022 published: Print-Electronic CommentIn: J Eur Acad Dermatol Venereol. 2022 Dec;36(12):e988-e989. - PMID 35790032 Citation Status MEDLINE |
---|
doi: |
10.1111/jdv.17981 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM336548702 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM336548702 | ||
003 | DE-627 | ||
005 | 20231225232407.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1111/jdv.17981 |2 doi | |
028 | 5 | 2 | |a pubmed24n1121.xml |
035 | |a (DE-627)NLM336548702 | ||
035 | |a (NLM)35122335 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Neagu, N |e verfasserin |4 aut | |
245 | 1 | 0 | |a Dupilumab ocular side effects in patients with atopic dermatitis |b a systematic review |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 12.05.2022 | ||
500 | |a Date Revised 15.11.2022 | ||
500 | |a published: Print-Electronic | ||
500 | |a CommentIn: J Eur Acad Dermatol Venereol. 2022 Dec;36(12):e988-e989. - PMID 35790032 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2022 European Academy of Dermatology and Venereology. | ||
520 | |a Atopic dermatitis (AD) is a chronic, inflammatory skin disorder that most frequently occurs in children, but it can also affect adults. Even though most AD cases can be managed with topical treatments, moderate-to-severe forms require systemic therapies. Dupilumab is the first human monoclonal antibody approved for the treatment of AD. Its action is through IL-4 receptor alpha subunit inhibition, thus blocking IL-4 and IL-13 signaling pathways. It has been shown to be an effective, well-tolerated therapy for AD, as well as for asthma, chronic rhinosinusitis with nasal polyposis (CRSwNP), and eosinophilic esophagitis (EoE). However, an increasing incidence of dupilumab-induced ocular surface disease (DIOSD) has been reported in patients treated with dupilumab, as compared to placebo. The aim of this study was to summarize scientific data regarding DIOSD in AD patients treated with dupilumab. A search of PubMed and clinicaltrials.gov databases was performed. There was no limit to study design. All AD cases were moderate-to-severe. DIOSD was either dermatologist-, allergist-, or ophthalmologist-assessed. Evidence shows that DIOSD occurs most frequently in patients with atopic dermatitis and not in other skin conditions, neither in patients with asthma, CRSwNP, nor EoE who are on dupilumab treatment. Further studies are warranted in order to establish a causal relationship between dupilumab and ocular surface disease. Nevertheless, ophthalmological evaluations prior to dupilumab initiation can benefit AD patients with previous ocular pathology or current ocular symptomatology. Also, patch testing for ocular allergic contact dermatitis might be advantageous in patients with a history of allergic conjunctivitis. Furthermore, TARC, IgE, and circulating eosinophils levels might be important biomarkers for a baseline assessment of future candidates to dupilumab treatment. However, TARC measurements should be resumed for research purposes only | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
650 | 4 | |a Systematic Review | |
650 | 7 | |a Antibodies, Monoclonal, Humanized |2 NLM | |
650 | 7 | |a Interleukin-4 Receptor alpha Subunit |2 NLM | |
650 | 7 | |a dupilumab |2 NLM | |
650 | 7 | |a 420K487FSG |2 NLM | |
700 | 1 | |a Dianzani, C |e verfasserin |4 aut | |
700 | 1 | |a Avallone, G |e verfasserin |4 aut | |
700 | 1 | |a Dell'Aquila, C |e verfasserin |4 aut | |
700 | 1 | |a Morariu, S-H |e verfasserin |4 aut | |
700 | 1 | |a Zalaudek, I |e verfasserin |4 aut | |
700 | 1 | |a Conforti, C |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of the European Academy of Dermatology and Venereology : JEADV |d 1997 |g 36(2022), 6 vom: 15. Juni, Seite 820-835 |w (DE-627)NLM091705932 |x 1468-3083 |7 nnns |
773 | 1 | 8 | |g volume:36 |g year:2022 |g number:6 |g day:15 |g month:06 |g pages:820-835 |
856 | 4 | 0 | |u http://dx.doi.org/10.1111/jdv.17981 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 36 |j 2022 |e 6 |b 15 |c 06 |h 820-835 |