Rapid and Continuing Improvements in Nasal Symptoms with Dupilumab in Patients with Severe CRSwNP

被引:11
作者
Bachert, Claus [1 ,2 ,3 ,4 ]
Khan, Asif H. [5 ]
Hopkins, Claire [6 ]
Blaiss, Michael S. [7 ]
Soler, Zachary M. [8 ]
Nash, Scott [9 ]
Siddiqui, Shahid [9 ]
Praestgaard, Amy [10 ]
Deniz, Yamo [9 ]
Rowe, Paul J. [11 ]
Jacob-Nara, Juby A. [11 ]
机构
[1] Univ Ghent, Upper Airways Res Lab, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Otorhinolaryngol, B-9000 Ghent, Belgium
[3] Karolinska Inst, Div ENT Dis, CLINTEC, Stockholm, Sweden
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Int Airway Res Ctr, Guangzhou, Peoples R China
[5] Sanofi, Global Med Affairs, Chilly Mazarin, France
[6] Guys & St Thomas Hosp, Dept Otorhinolaryngol Head & Neck Surg, London, England
[7] Augusta Univ, Med Coll Georgia, Dept Pediat, Augusta, GA USA
[8] Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, Charleston, SC 29425 USA
[9] Regeneron Pharmaceut Inc, Med Affairs, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[10] Sanofi, Dept Biostat, Cambridge, MA USA
[11] Sanofi, Global Med Affairs, Bridgewater, NJ USA
关键词
chronic rhinosinusitis with nasal polyps; dupilumab; nasal polyp score; nasal congestion;
D O I
10.2147/JAA.S355391
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: In the phase 3 SINUS-24 (NCT02912468) and SINUS-52 (NCT02898454) studies in adults with severe chronic rhinosinusitis with nasal polyps (CRSwNP), dupilumab significantly improved the co-primary endpoints of change from baseline to Week 24 in nasal polyp score (NPS) and nasal congestion/obstruction (NC) vs placebo on background intranasal corticosteroids (standard of care [SOC]). This post hoc analysis of SINUS-24/-52 investigated the direction and magnitude of within-patient change in these endpoints over time. Methods: NPS (scale 0-8) was assessed at Weeks 4, 8, 16, 24, 40, and 52 in SINUS-52 and Weeks 8, 16, and 24 in SINUS-24. Daily patient-reported NC scores (0 [no symptoms]-3 [severe symptoms]) were averaged over 28 days. Within-patient changes from baseline were assessed through Week 24 in pooled SINUS-24/-52 (n = 438/286 dupilumab/SOC) and through Week 52 in SINUS-52 (n = 150/153). Results: In SINUS-52, NPS improved in 70.0% of dupilumab-treated patients at Week 4 vs 31.8% with SOC (odds ratio [OR] 5.2 [95% confidence interval 3.1-8.8]) and 78.7% vs 28.2% at Week 52 (OR 10.6 [6.0-18.7]) (all p < 0.0001). NC improved in 73.3% of dupilumab-treated patients at Week 4 vs 46.7% with SOC (OR 3.2 [2.0-5.3]) and 86.9% vs 50.7% at Week 52 (OR 6.4 [3.5-11.5]) (all p < 0.0001). Clinically meaningful (>= 1 point) improvements in NPS occurred in 55.7% and 72.3% of dupilumab-treated patients at Weeks 4 and 52, respectively, vs 16.9% and 16.2% with SOC. Clinically meaningful (>= 1 point) improvements in NC occurred in 16.7% and 67.6% of dupilumab-treated patients at Weeks 4 and 52, respectively, vs 3.9% and 20.8% with SOC. At Week 52, NPS worsening from baseline was observed in 5.7% of dupilumab-treated patients vs 40.1% with SOC and NC worsening in 2.1% vs 20.8%, respectively. Conclusion: Dupilumab provided rapid, continuing, and clinically relevant improvements over time in NPS and NC in most patients with severe CRSwNP in the SINUS studies.
引用
收藏
页码:557 / 563
页数:7
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