Real-life evaluation of the clinical, functional, and hematological effects of mepolizumab in patients with severe eosinophilic asthma: Results of a single-centre observational study

被引:57
作者
Pelaia, Corrado [1 ]
Busceti, Maria Teresa [1 ]
Solinas, Sabina [1 ]
Terracciano, Rosa [2 ]
Pelaia, Girolamo [1 ]
机构
[1] Magna Graecia Univ Catanzaro, Sect Resp Dis, Dept Med & Surg Sci, Catanzaro, Italy
[2] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Catanzaro, Italy
关键词
Severe eosinophilic asthma; Exacerbations; IL-5; Mepolizumab; DOUBLE-BLIND; INTERLEUKIN-5; BENRALIZUMAB; INFLAMMATION; MULTICENTER; EFFICACY; THERAPY; EXACERBATIONS; BIOLOGICS; SAFETY;
D O I
10.1016/j.pupt.2018.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mepolizumab is a humanized monoclonal antibody which targets interleukin-5 (IL-5) and is nowadays available in many countries for add-on biological therapy of severe eosinophilic asthma. Although the approval of mepolizumab use in clinical practice has been made possible by several successful pre-marketing controlled trials, so far only a very few studies have been performed in a real-life setting. Within such a context, our present observational investigation refers to 14 patients with refractory eosinophilic asthma, currently treated with mepolizumab at the Respiratory Unit of "Magna Griecia" University Hospital located in Catanzaro, Italy, whose anti-IL-5 treatment began between June 2017 and January 2018. These patients experienced a significant increase in asthma control test (ACT) score, that was evaluated at baseline (13.64 +/- 3.00), as well as after 4 weeks (18.86 +/- 3.15; p < 0.0001) and 24 weeks (20.07 +/- 1.94; p < 0.0001) of add-on therapy with mepolizumab. This relevant improvement in symptom control was paralleled by a dramatic fall of blood eosinophil numbers, counted at baseline (647.1 +/- 274.7 cells/mu l), and at the 4th (147.8 +/- 66.5 cells/mu l; p < 0.0001) and 24th week (98.6 +/- 40.3 cells/mu l; p < 0.0001) after starting add-on treatment with mepolizumab. These changes were associated with significant and stable increases in FEV1, which was recorded at baseline (1389 +/- 454.3 mL), as well as after 4 weeks (1711 +/- 482.3 mL; p < 0.001) and 24 weeks (1701 +/- 456.0 mL; p < 0.01). Moreover, in comparison to the 6 months preceding the beginning of treatment with mepolizumab, after 24 weeks of anti-IL-5 therapy significant decreases were detected with regard to exacerbation numbers (from 3.64 +/- 1.86 to 1.0 +/- 0.78; p < 0.001) and oral intake of prednisone (from 24.11 +/- 10.36 mg/day to 1.78 +/- 3.82 mg/day). Therefore, these preliminary data referring to our single-centre observational study corroborate, in a real-life environment, the efficacy of mepolizumab for treatment of patients with exacerbation-prone, corticosteroid-refractory, severe eosinophilic asthma.
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页码:1 / 5
页数:5
相关论文
共 42 条
  • [11] Targeting eosinophils in allergy, inflammation and beyond
    Fulkerson, Patricia C.
    Rothenberg, Marc E.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2013, 12 (02) : 117 - 129
  • [12] Update on Anticytokine Treatment for Asthma
    Gallelli, Luca
    Busceti, Maria Teresa
    Vatrella, Alessandro
    Maselli, Rosario
    Pelaia, Girolamo
    [J]. BIOMED RESEARCH INTERNATIONAL, 2013, 2013
  • [13] Gnanakumaran G, 2003, CURR OPIN MOL THER, V5, P321
  • [14] Evaluation of Potential Continuation Rules for Mepolizumab Treatment of Severe Eosinophilic Asthma
    Gunsoy, Necdet B.
    Cockle, Sarah M.
    Yancey, Steven W.
    Keene, Oliver N.
    Bradford, Eric S.
    Albers, Frank C.
    Pavord, Ian D.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2018, 6 (03) : 874 - +
  • [15] Asthma
    Holgate, Stephen T.
    Wenzel, Sally
    Postma, Dirkje S.
    Weiss, Scott T.
    Renz, Harald
    Sly, Peter D.
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2015, 1
  • [16] The Asthma Control Test and Asthma Control Questionnaire for assessing asthma control: Systematic review and meta-analysis
    Jia, Chun E.
    Zhang, Hong Ping
    Lv, Yan
    Liang, Rui
    Jiang, Yun Qiu
    Powell, Heather
    Fu, Juan Juan
    Wang, Lei
    Gibson, Peter Gerard
    Wang, Gang
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 131 (03) : 695 - 703
  • [17] Prospective Open-Label Study of 48-Week Subcutaneous Administration of Mepolizumab in Japanese Patients With Severe Eosinophilic Asthma
    Kurosawa, M.
    Sutoh, E.
    [J]. JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2019, 29 (01) : 40 - 45
  • [18] Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response
    Leckie, MJ
    ten Brinke, A
    Khan, J
    Diamant, Z
    O'Connor, BJ
    Walls, CM
    Mathur, AK
    Cowley, HC
    Chung, KF
    Djukanovic, R
    Hansel, TT
    Holgate, T
    Sterk, PJ
    Barnes, PJ
    [J]. LANCET, 2000, 356 (9248) : 2144 - 2148
  • [19] Long-term Efficacy and Safety of Mepolizumab in Patients With Severe Eosinophilic Asthma: A Multi-center, Open-label, Phase IIIb Study
    Lugogo, Njira
    Domingo, Christian
    Chanez, Pascal
    Leigh, Richard
    Gilson, Martyn J.
    Price, Robert G.
    Yancey, Steven W.
    Ortega, Hector G.
    [J]. CLINICAL THERAPEUTICS, 2016, 38 (09) : 2058 - 2070
  • [20] Benralizumab for the treatment of asthma
    Matera, M. G.
    Rogliani, P.
    Calzetta, L.
    Canonica, G. W.
    Cazzola, M.
    [J]. DRUGS OF TODAY, 2017, 53 (12) : 633 - 645