Otani Iris M, Lumry William R, Hurwitz Shelley, Li Huamin Henry, Craig Timothy J, Holtzman Niki S, Iandoli Matthew I, Tucker Julie, Riedl Marc A, Zuraw Bruce L, Banerji Aleena
Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Mass.
Allergy Asthma Research Associates Research Center, Dallas, Texas; Allergy and Asthma Specialists, Dallas, Texas.
J Allergy Clin Immunol Pract. 2017 Mar-Apr;5(2):442-447.e1. doi: 10.1016/j.jaip.2016.09.023. Epub 2016 Nov 3.
Hereditary angioedema (HAE) is a life-threatening disorder characterized by recurrent angioedema. Icatibant, a subcutaneous bradykinin-B2-receptor antagonist, is an effective on-demand therapy. Data outside the United States suggest that self-administration is tolerated and patient-preferred compared with administration by health care professionals at medical facilities (HCP-administration).
A prospective, multicenter study was conducted in the United States to compare icatibant self-administration and HCP-administration.
Subjects 18 years or older with type I or II HAE were recruited. The first 2 HAE attacks after enrollment were treated at medical facilities. Subjects were instructed by a health care professional on self-administration during icatibant treatment for the second HAE attack. Icatibant was self-administered for all subsequent attacks. For each treated HAE attack, efficacy, safety, and tolerability data were recorded.
Nineteen patients with HAE received icatibant for 79 distinct HAE attacks. Mean attack duration was significantly shorter with self-administration (n = 50; 547 ± 510 minutes) than with HCP-administration (n = 29; 968 ± 717 minutes; P = .006). Mean time to treatment was significantly shorter with self-administration (143 ± 226 minutes) than with HCP-administration (361 ± 503 minutes; P < .0001). Shorter times to treatment were associated with shorter time from treatment to symptom resolution (r = 0.35; P = .02). Improvements in visual analog scale score and patient symptom score from pretreatment to 4 hours postinjection were comparable between self-administration and HCP-administration. There were no serious adverse events or discontinuations due to adverse events with self-administration or HCP-administration.
Icatibant self-administration shortened attack duration and time to treatment, with no difference in safety or local tolerability compared with HCP-administration. These findings support icatibant as an effective on-demand option for home-based treatment.
遗传性血管性水肿(HAE)是一种以反复发作的血管性水肿为特征的危及生命的疾病。艾替班特是一种皮下注射的缓激肽B2受体拮抗剂,是一种有效的按需治疗药物。美国以外的数据表明,与在医疗机构由医护人员给药(HCP给药)相比,自我给药是可耐受的且患者更倾向于选择。
在美国进行了一项前瞻性多中心研究,以比较艾替班特自我给药和HCP给药的情况。
招募18岁及以上的I型或II型HAE患者。入组后的前2次HAE发作在医疗机构接受治疗。在艾替班特治疗第二次HAE发作期间,医护人员指导患者进行自我给药。所有后续发作均由患者自我给药。对于每次接受治疗的HAE发作,记录疗效、安全性和耐受性数据。
19例HAE患者接受艾替班特治疗了79次不同的HAE发作。自我给药组(n = 50;547±510分钟)的平均发作持续时间明显短于HCP给药组(n = 29;968±717分钟;P = .006)。自我给药组的平均治疗时间(143±226分钟)明显短于HCP给药组(361±503分钟;P < .0001)。较短的治疗时间与从治疗到症状缓解的较短时间相关(r = 0.35;P = .02)。自我给药和HCP给药在从注射前到注射后4小时的视觉模拟量表评分和患者症状评分改善方面相当。自我给药或HCP给药均未出现严重不良事件或因不良事件而停药的情况。
艾替班特自我给药缩短了发作持续时间和治疗时间,与HCP给药相比,安全性或局部耐受性无差异。这些发现支持艾替班特作为一种有效的家庭按需治疗选择。