Schlösser Anne R, Bult Lotte, Thelen John C, Thiadens Alberta A H J, Schappin Renske, Nijsten Tamar E C, Veen Johannes C C M In 't, Braunstahl Gerrit J, Hijnen DirkJan
Department of Dermatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Department of Pulmonology, Franciscus Gasthuis and Vlietland, Rotterdam, The Netherlands.
Clin Transl Allergy. 2024 Aug;14(8):e12386. doi: 10.1002/clt2.12386.
Dupilumab has been shown to be an effective treatment in moderate-to-severe atopic dermatitis (AD) and severe asthma (SA). However, comparative real-world analyses of adverse events (AE), particularly dupilumab-associated ocular surface disease (DAOSD), are lacking.
This is the first real-world study to provide insight into the prevalence of AEs associated with dupilumab in AD compared with SA. Secondary objectives were to assess the prevalence, onset and therapeutic strategies of DAOSD and evaluate dupilumab discontinuation rates.
Data from two daily practice registries including AD and SA patients receiving dupilumab treatment were analyzed. Adverse events, including DAOSD, were evaluated.
In total, 322 AD and 148 SA patients were included. Headaches (23.6%), injection site reactions (10.1%), and influenza-like symptoms (13.5%) were more prevalent in SA patients. Interestingly, ocular AEs were significantly more prevalent in AD patients (62.1%, p < 0.001), including conjunctivitis (17.1%, p = 0.004). 88% AD and 47% SA patients with ocular AEs received one or more ophthalmic treatment(s). Additionally, 20% of AD and 17.6% of SA patients discontinued dupilumab treatment due to ocular AEs, while only 65% of these AD and none of these SA patients were referred to an ophthalmologist.
The higher incidence of DAOSD in AD patients compared with SA patients in this real-world study highlights the importance of physician awareness, especially when prescribing dupilumab to AD patients. Conversely, the findings of this study help alleviate potential concerns about ocular AEs in patients with SA who do not have comorbid AD. Furthermore, the effective management of most ocular AEs with ophthalmic treatments suggests favorable tolerability of dupilumab in daily practice, and multidisciplinary collaboration is essential to proactively manage ocular AEs before discontinuing dupilumab.
度普利尤单抗已被证明是治疗中度至重度特应性皮炎(AD)和重度哮喘(SA)的有效药物。然而,缺乏对不良事件(AE),尤其是与度普利尤单抗相关的眼表疾病(DAOSD)的比较性真实世界分析。
这是第一项真实世界研究,旨在深入了解与度普利尤单抗相关的AD患者与SA患者不良事件的发生率。次要目标是评估DAOSD的发生率、发病情况和治疗策略,并评估度普利尤单抗的停药率。
分析了来自两个日常实践登记处的数据,这些数据包括接受度普利尤单抗治疗的AD和SA患者。对包括DAOSD在内的不良事件进行了评估。
总共纳入了322例AD患者和148例SA患者。SA患者中头痛(23.6%)、注射部位反应(10.1%)和流感样症状(13.5%)更为常见。有趣的是,AD患者中眼部不良事件明显更为常见(62.1%,p < 0.001),包括结膜炎(17.1%,p = 0.004)。88%的AD眼部不良事件患者和47%的SA眼部不良事件患者接受了一种或多种眼科治疗。此外,20%的AD患者和17.6%的SA患者因眼部不良事件停用了度普利尤单抗治疗,而这些AD患者中只有65%被转诊至眼科医生,这些SA患者均未转诊。
在这项真实世界研究中,AD患者与SA患者相比,DAOSD的发生率更高,这突出了医生提高认识的重要性,尤其是在给AD患者开度普利尤单抗处方时。相反,本研究结果有助于减轻对无合并AD的SA患者眼部不良事件的潜在担忧。此外,大多数眼部不良事件通过眼科治疗有效管理,这表明度普利尤单抗在日常实践中具有良好的耐受性,多学科协作对于在停用度普利尤单抗之前积极管理眼部不良事件至关重要。