Busse William Walter, Pavord Ian Douglas, Siddiqui Shahid, Khan Asif Hameed, Praestgaard Amy, Nash Scott, Jacob-Nara Juby Anne, Rowe Paul Jonathan, Deniz Yamo
Department of Medicine, Division of Allergy, Pulmonary and Critical Care, University of Wisconsin, Madison, WI, USA.
Oxford Respiratory NIHR BRC, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
J Asthma Allergy. 2023 Apr 18;16:411-419. doi: 10.2147/JAA.S391896. eCollection 2023.
Chronic rhinosinusitis with nasal polyps (CRSwNP) is a predominantly type 2 inflammatory disease frequently coexisting with other type 2 conditions including asthma and non-steroidal anti-inflammatory drug-exacerbated respiratory disease (NSAID-ERD). Coexisting asthma leads to increased CRSwNP symptom burden. Dupilumab, a monoclonal antibody that blocks the shared receptor component for interleukin-4 and -13, demonstrated efficacy in adults with severe CRSwNP in the Phase 3 SINUS-24 (NCT02912468) and SINUS-52 (NCT02898454) studies, including in patients with coexisting asthma/NSAID-ERD. However, the impact of different asthma characteristics on dupilumab treatment in this population is unknown. We report CRSwNP and asthma outcomes with dupilumab in patients with CRSwNP and coexisting asthma according to baseline asthma characteristics.
Change from baseline at Week 24 (pooled studies) and Week 52 (SINUS-52) in CRSwNP outcomes (nasal polyp score, nasal congestion, 22-item Sino-Nasal Outcome Test [SNOT-22], loss of smell score, University of Pennsylvania Smell Identification Test) and asthma outcomes (5-item Asthma Control Questionnaire [ACQ-5], pre-bronchodilator forced expiratory volume in 1 second [FEV]) were analyzed post hoc for placebo and dupilumab 300 mg every 2 weeks according to baseline blood eosinophils ≥150/≥300 cells/µL, ACQ-5 scores <1.5/≥1.5, and FEV <80%.
In the pooled studies, 428/724 patients (59.1%) had coexisting asthma, of which 181/428 (42.3%) had coexisting NSAID-ERD. Dupilumab significantly improved all CRSwNP and asthma outcomes vs placebo at Week 24 (P < 0.001) regardless of baseline eosinophil or ACQ-5 category, or FEV <80%. Similar magnitude of improvement was seen at Week 52 (SINUS-52) and in patients with NSAID-ERD (pooled studies, Week 24). By Week 24, improvements with dupilumab exceeded the minimum clinically important differences for ACQ-5 and SNOT-22 in 35.2% to 74.2% and 72.0% to 78.7% of patients, respectively.
Dupilumab improved CRSwNP outcomes in patients with CRSwNP and coexisting asthma, and improved asthma outcomes, regardless of differences in baseline asthma characteristics.
伴有鼻息肉的慢性鼻-鼻窦炎(CRSwNP)是一种主要的2型炎症性疾病,常与其他2型疾病共存,包括哮喘和非甾体抗炎药加重的呼吸道疾病(NSAID-ERD)。共存的哮喘会导致CRSwNP症状负担加重。度普利尤单抗是一种阻断白细胞介素-4和-13共享受体成分的单克隆抗体,在3期SINUS-24(NCT02912468)和SINUS-52(NCT02898454)研究中,已证明其对重度CRSwNP成人患者有效,包括对共存哮喘/NSAID-ERD的患者。然而,不同哮喘特征对该人群度普利尤单抗治疗的影响尚不清楚。我们根据基线哮喘特征报告了度普利尤单抗治疗CRSwNP合并共存哮喘患者的CRSwNP和哮喘结局。
在汇总研究的第24周(合并研究)和第52周(SINUS-52),根据基线血嗜酸性粒细胞≥150/≥300细胞/µL、哮喘控制问卷-5(ACQ-5)评分<1.5/≥1.5以及第1秒用力呼气容积(FEV)<80%,对CRSwNP结局(鼻息肉评分、鼻充血、22项鼻鼻窦结局测试[SNOT-22]、嗅觉丧失评分、宾夕法尼亚大学嗅觉识别测试)和哮喘结局(5项哮喘控制问卷[ACQ-5]、支气管扩张剂前1秒用力呼气容积[FEV])相对于基线的变化进行事后分析,比较安慰剂和每2周一次300mg度普利尤单抗的疗效。
在汇总研究中,428/724例患者(59.1%)共存哮喘,其中181/428例(42.3%)共存NSAID-ERD。在第24周时,无论基线嗜酸性粒细胞或ACQ-5类别,还是FEV<80%,度普利尤单抗相对于安慰剂均显著改善了所有CRSwNP和哮喘结局(P<0.001)。在第52周(SINUS-52)以及共存NSAID-ERD的患者中(汇总研究,第24周)也观察到了相似程度的改善。到第24周时,度普利尤单抗治疗使分别有35.2%至74.2%和72.0%至78.7%的患者的ACQ-5和SNOT-22改善超过最小临床重要差异。
度普利尤单抗改善了CRSwNP合并共存哮喘患者的CRSwNP结局,并改善了哮喘结局,无论基线哮喘特征存在何种差异。