Dupilumab has an additional benefit in treatment of chronic rhinosinusitis with nasal polyps

被引:1
|
作者
Klimek, L. [1 ]
Chaker, A. [2 ]
Deitmer, T. [3 ]
Plontke, S. K. [4 ]
Wollenberg, B. [2 ]
Bousquet, J. [5 ,6 ,7 ,8 ,9 ]
Bachert, C. [10 ]
机构
[1] Univ Med Mainz, Allergiezentrum Rheinland Pfalz, Wiesbaden, Germany
[2] Tech Univ Munich, Klin Hals Nasen & Ohrenheilkunde, Munich, Germany
[3] Deutsch Gesell Hals Nasen & Ohrenheilkunde Kopf &, Bonn, Germany
[4] Univ Klinikum Halle, Klin Hals Nasen & Ohrenheilkunde, Halle, Germany
[5] Charite, Klin Dermatol Venerol & Allergol, Berlin Inst Hlth, Comprehens Allergy Ctr, Berlin, Germany
[6] Fdn Partenariale FMC VIA LR, MACVIA France, Montpellier, France
[7] VIMA Ageing & Chron Dis Epidemiol & Publ Hlth App, INSERM, U1168, Villejuif, France
[8] Univ Versailles St Quentin En Yvelines, UMR S 1168, Montigny Le Bretonneux, France
[9] Univ Klinikum Gent, Klin Hals Nasen & Ohrenheilkunde, Ghent, Belgium
[10] Zentrum Rhinol & Allergol Wiesbaden, Quellen 10, D-65183 Wiesbaden, Germany
关键词
Type-2-inflammation; AMNOG procedure; CRSwNP; Biologics; Dupilumab; Additional approval; ENDOSCOPIC SINUS SURGERY; GERMAN SOCIETY; EPIDEMIOLOGY; INTOLERANCE; GUIDELINE; HEAD; AEDA;
D O I
10.1007/s00106-021-01018-z
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background For patients with severe chronic rhinosinusitis with nasal polyps (CRSwNP) which cannot be controlled by continuous therapy with intranasal corticosteroids (INCS) and systemic corticosteroids and/or surgical treatment, there were no approved curative options for a long time. For CRSwNP treatment with T2-addressing biologics is possible. On October 24, 2019, the European Commission granted extended approval for dupilumab as the first biological agent for treatment of insufficiently controlled severe CRSwNP. The Federal Joint Committee (G-BA) evaluates the benefits of reimbursable drugs with new active ingredients. This includes assessment of the additional benefit and its therapeutic relevance. Methods A meta-analysis was performed using individual patient data based on two phase III studies. Both studies examined the safety and efficacy of dupilumab as an add-on therapy to INCS for treatment of CRSwNP in adults inadequately controlled with systemic corticosteroids and/or surgery compared to INCS alone. Results Based on the present data, the G-BA decided that there is an indication of a considerable additional benefit of dupilumab compared to mometasone furoate. Conclusion For patients with severe CRSwNP inadequately controlled with INCS and systemic corticosteroids and/or surgery, there is an indication of a considerable additional benefit for the administration of dupilumab as an add-on therapy to INCS compared to mometasone furoate alone.
引用
收藏
页码:868 / 877
页数:10
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