Conjunctivitis in dupilumab clinical trials

被引:346
作者
Akinlade, B. [1 ]
Guttman-Yassky, E. [2 ]
de Bruin-Weller, M. [3 ]
Simpson, E. L. [4 ]
Blauvelt, A. [5 ]
Cork, M. J. [6 ]
Prens, E. [7 ]
Asbell, P. [8 ]
Akpek, E. [9 ]
Corren, J. [10 ]
Bachert, C. [11 ,12 ]
Hirano, I. [13 ]
Weyne, J. [1 ]
Korotzer, A. [1 ]
Chen, Z. [1 ]
Hultsch, T. [14 ]
Zhu, X. [1 ]
Davis, J. D. [1 ]
Mannent, L. [15 ]
Hamilton, J. D. [1 ]
Teper, A. [16 ]
Staudinger, H. [16 ]
Rizova, E. [14 ]
Pirozzi, G. [16 ]
Graham, N. M. H. [1 ]
Shumel, B. [1 ]
Ardeleanu, M. [1 ]
Wollenberg, A. [17 ]
机构
[1] Regeneron Pharmaceut Inc, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[2] Icahn Sch Med Mt Sinai, Dept Dermatol, Med Ctr, New York, NY 10029 USA
[3] Univ Med Ctr Utrecht, Dept Dermatol & Allergol, Utrecht, Netherlands
[4] Oregon Hlth & Sci Univ, Dept Dermatol, Portland, OR 97201 USA
[5] Oregon Med Res Ctr, Portland, OR USA
[6] Univ Sheffield, Sheffield Dermatol Res, Dept Infect Immun & Cardiovasc Dis, Sch Med, Sheffield, S Yorkshire, England
[7] Erasmus MC, Dept Dermatol, Rotterdam, Netherlands
[8] Univ Tennessee, Ctr Hlth Sci, Hamilton Eye Inst, Memphis, TN 38163 USA
[9] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
[10] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[11] Ghent Univ Hosp, ENT Dept, Ghent, Belgium
[12] Karolinska Inst, Dept Clin Sci Intervent & Technol CLINTEC, Stockholm, Sweden
[13] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[14] Sanofi Genzyme, Cambridge, MA USA
[15] Sanofi R&D, Chilly Mazarin, France
[16] Sanofi, Bridgewater, NJ USA
[17] Ludwig Maximilians Univ Munchen, Munich, Germany
关键词
ATOPIC-DERMATITIS PATIENTS; 2-PHASE; 3; TRIALS; DRY EYE DISEASE; OCULAR COMPLICATIONS; PERSISTENT ASTHMA; BARRIER FUNCTION; DOUBLE-BLIND; PLACEBO; PREVALENCE; ADULTS;
D O I
10.1111/bjd.17869
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Dupilumab blocks the shared receptor component for interleukin (IL)-4 and IL-13. It is approved in the U.S.A. for patients aged >= 12 years with moderate-to-severe atopic dermatitis (AD) uncontrolled by topical prescription medicines or who cannot use topical medicines, for patients in Japan whose AD is uncontrolled with existing therapies, for patients with moderate-to-severe AD in Europe who are candidates for systemic therapy and for patients aged >= 12 years for maintenance treatment of moderate-to-severe asthma uncontrolled with their current medicines. AD trials have reported increased incidence of conjunctivitis for dupilumab vs. placebo. Objectives To characterize further the occurrence and risk factors of conjunctivitis in dupilumab clinical trials. Methods We evaluated randomized placebo-controlled trials of dupilumab in AD (n = 2629), asthma (n = 2876), chronic rhinosinusitis with nasal polyps (CRSwNP) (n = 60) and eosinophilic oesophagitis (EoE) (n = 47). Results In most AD trials, dupilumab-treated patients had higher conjunctivitis incidence than placebo controls. Higher baseline AD severity and previous history of conjunctivitis were associated with increased conjunctivitis incidence. Conjunctivitis was mostly mild to moderate. Most cases recovered or resolved during the treatment period; two patients permanently discontinued dupilumab due to conjunctivitis or keratitis. Common treatments included ophthalmic corticosteroids, antibiotics, and antihistamines or mast cell stabilizers. Most cases were diagnosed by the investigators. In asthma and CRSwNP trials, the incidence of conjunctivitis was lower for both dupilumab and placebo than in AD trials; dupilumab did not increase the incidence compared with placebo. In the EoE trial, no patients had conjunctivitis. Conclusions Conjunctivitis was more frequent with dupilumab treatment in most AD trials. In dupilumab trials in other type 2 diseases, incidence of conjunctivitis was overall very low, and was similar for dupilumab and placebo. In AD, the incidence of conjunctivitis was associated with AD severity and prior history of conjunctivitis. The aetiology and treatment of conjunctivitis in dupilumab-treated patients require further study. What's already known about this topic? Ocular disorders, including allergic conjunctivitis, are common in patients with atopic dermatitis (AD). In most dupilumab AD trials, dupilumab-treated patients had higher conjunctivitis incidence than those receiving placebo. Most cases were mild to moderate and recovered or were recovering during study treatment; study treatment discontinuation due to conjunctivitis was rare. Conjunctivitis incidence was very low and similar for dupilumab and placebo in clinical trials in asthma, chronic rhinosinusitis with nasal polyps and eosinophilic oesophagitis. What does this study add? This analysis confirms and extends the results of the individual clinical trials. Baseline disease-related factors, including AD severity, prior conjunctivitis history and certain biomarkers (thymus and activation-regulated chemokine, IgE, eosinophils), were associated with increased incidence of conjunctivitis. Patients who responded well to dupilumab had reduced incidence of conjunctivitis. Further study is needed to elucidate the aetiology and treatment of conjunctivitis in dupilumab-treated patients with AD.
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收藏
页码:459 / 473
页数:15
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