Menzella Francesco, Galeone Carla, Lusuardi Mirco, Simonazzi Anna, Castagnetti Claudia, Ruggiero Patrizia, Facciolongo Nicola
Department of Medical Specialties, Pneumology Unit, Arcispedale Santa Maria Nuova - IRCCS, Azienda USL di Reggio Emilia, Reggio Emilia.
Unit of Respiratory Rehabilitation, Azienda USL di Reggio Emilia, S. Sebastiano Hospital, Correggio, Italy.
Ther Clin Risk Manag. 2017 Nov 8;13:1489-1493. doi: 10.2147/TCRM.S149775. eCollection 2017.
Severe asthma affects between 5% and 10% of patients with asthma worldwide and requires best standard therapies at maximal doses, but there is a subgroup of patients refractory to all treatments. We share a case report of a 53-year-old woman with a history of severe allergic asthma that progressively worsened over the years despite the best therapy. She had been hospitalized 35 times, including nine admissions to the respiratory intensive care unit due to severe exacerbations. To rule out other possible diagnoses, several investigations were performed, such as computed tomography scan of the chest and neck, fiberoptic laryngoscopy, antineutrophil cytoplasmic antibodies, and complete blood cell count. The patient was first treated with omalizumab, which was completely ineffective, and then with bronchial thermoplasty (BT), again without clinical benefit. The situation remained critical for about 3 months during the last hospitalization, but in February 2017, the Italian Medicines Agency approved the treatment of severe refractory eosinophilic asthma with mepolizumab (Nucala). Given a blood eosinophil count of 300 cells/μL, our patient was started on 100 mg mepolizumab treatment. After the second administration, symptoms improved progressively, with a reduction in the number and severity of exacerbations, so the patient could finally be discharged from hospital. At follow-up, it was possible to reduce and then suspend oral corticosteroids by continuing only with inhaled corticosteroids/long-acting beta-agonists and montelukast. No further asthmatic exacerbations occurred; symptom control and quality of life improved significantly. To our knowledge, this is the first case of a patient unresponsive to omalizumab and BT but with excellent clinical response to mepolizumab. She is also the first patient to be treated with an anti-IL5 agent in Italy in a real-life clinical setting. The availability of new effective biological agents will allow many patients to resume as normal a life as possible, with a positive outcome also from a social and economic point of view.
全球范围内,重度哮喘影响着5%至10%的哮喘患者,需要采用最大剂量的最佳标准疗法进行治疗,但仍有一部分患者对所有治疗均无反应。我们分享一例53岁女性的病例报告,该患者有重度过敏性哮喘病史,尽管接受了最佳治疗,但病情多年来逐渐恶化。她曾住院35次,其中9次因严重病情加重入住呼吸重症监护病房。为排除其他可能的诊断,进行了多项检查,如胸部和颈部计算机断层扫描、纤维喉镜检查、抗中性粒细胞胞浆抗体检测及全血细胞计数。该患者首先接受了奥马珠单抗治疗,但完全无效,随后接受了支气管热成形术(BT),同样未获得临床益处。在最后一次住院期间,病情危急持续了约3个月,但在2017年2月,意大利药品管理局批准了美泊利单抗(Nucala)用于治疗重度难治性嗜酸性粒细胞性哮喘。鉴于患者血液嗜酸性粒细胞计数为300个/μL,开始给予100mg美泊利单抗治疗。第二次给药后,症状逐渐改善,病情加重的次数和严重程度均有所减轻,患者最终得以出院。在随访中,通过仅继续使用吸入性糖皮质激素/长效β受体激动剂和孟鲁司特,有可能减少并随后停用口服糖皮质激素。此后未再发生哮喘加重;症状控制和生活质量显著改善。据我们所知,这是首例对奥马珠单抗和BT无反应但对美泊利单抗有出色临床反应的患者。她也是意大利在实际临床环境中首例接受抗IL-5药物治疗的患者。新型有效生物制剂的出现将使许多患者能够尽可能恢复正常生活,从社会和经济角度来看也会产生积极的结果。