Masitinib, a c-kit/PDGF receptor tyrosine kinase inhibitor, improves disease control in severe corticosteroid-dependent asthmatics

被引:107
作者
Humbert, M. [1 ]
de Blay, F. [2 ]
Garcia, G. [1 ]
Prud'homme, A. [3 ]
Leroyer, C. [4 ]
Magnan, A. [5 ,6 ,7 ]
Tunon-de-Lara, J. -M. [8 ]
Pison, C. [9 ]
Aubier, M. [10 ]
Charpin, D. [11 ]
Vachier, I. [12 ]
Purohit, A. [2 ]
Gineste, P. [13 ]
Bader, T. [13 ]
Moussy, A. [13 ]
Hermine, O. [13 ,14 ]
Chanez, P. [12 ,15 ]
机构
[1] Univ Paris 11, Serv Pneumol & Reanimat Resp, Hop Antoine Beclere,INSERM, Assistance Publ Hop Paris,UPRES EA2705,U764,IFR13, F-92140 Clamart, France
[2] Univ Strasbourg, Hop Univ Strasbourg, Strasbourg, France
[3] Ctr Hosp Intercommunal, Serv Malad Resp, Tarbes, France
[4] CHU Cavale Blanche, Dept Med Interne & Pneumol, Brest, France
[5] INSERM, UMR915, Nantes, France
[6] Univ Nantes, Fac Med, Inst Thorax, Nantes, France
[7] CHU Nantes, Inst Thorax, Serv Pneumol, F-44035 Nantes 01, France
[8] Univ Bordeaux, INSERM, U885, Ctr Hosp Univ, Bordeaux, France
[9] CHU Grenoble, Dept Med Aigue Specialisee, F-38043 Grenoble, France
[10] Hop Bichat Claude Bernard, Serv Pneumol, F-75877 Paris, France
[11] Hop Nord Marseille, Serv Pneumol Allergol, Marseille, France
[12] CHU Montpellier, Hop Arnaud Villeneuve, Dept Malad Resp, Montpellier, France
[13] AB Sci, Paris, France
[14] Univ Paris V Rene Descartes, Serv Hematol, Ctr Reference Mastocytoses, CNRS,UMR 8147,Assistance Publ Hop Paris,Hop Necke, Paris, France
[15] Univ Aix Marseille 2, Serv Pneumoallergol, Hop St Marguerite, UMR 6020, Marseille, France
关键词
asthma; c-kit; platelet-derived growth factor; mast cells; tyrosine kinase inhibitors; IMATINIB; CYCLOSPORINE; MECHANISMS; TARGETS; ADULTS; AGENT; LUNG; KIT;
D O I
10.1111/j.1398-9995.2009.02122.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Masitinib is a tyrosine kinase inhibitor targeting stem cell factor receptor (c-kit) and platelet-derived growth factor (PDGF) receptor, which are expressed on several cell types including mast cells and bronchial structural cells, respectively. We hypothesized that c-kit and PDGF receptor inhibition may decrease bronchial inflammation and interfere with airway remodeling, which are crucial features of severe asthma. Objectives: The primary endpoint was the percent change from baseline in oral corticosteroids after 16 weeks of treatment. Change in asthma control (asthma control questionnaire), exacerbation rate, pulmonary function tests, rescue medication requirement and safety were secondary endpoints. Methods: A 16-week randomized, dose-ranging (3, 4.5, and 6 mg/kg/day), placebo-controlled study was undertaken in 44 patients with severe corticosteroid-dependent asthma who remained poorly controlled despite optimal asthma management. Results: At 16 weeks of treatment, a comparable reduction in oral corticosteroids was achieved with masitinib and placebo (median reduction of -78% and -57% in the masitinib and placebo arms, respectively). Despite this similar reduction, the Asthma Control Questionnaire score was significantly better in the masitinib arm as compared to placebo with a reduction by 0.99 unit at week 16 (P < 0.001) vs 0.43 unit in the placebo arm. Masitinib therapy was associated with more transient skin rash and edema. Conclusions: Masitinib, a c-kit and PDGF-receptor tyrosine kinase inhibitor, may represent an innovative avenue of treatment in corticosteroid-dependent asthma. These preliminary results warrant further long-term clinical studies in severe asthma (ClinicalTrials.gov Identifier: NCT00842270).
引用
收藏
页码:1194 / 1201
页数:8
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