Lumry William R, Miller Dave P, Newcomer Scott, Fitts David, Dayno Jeffrey
Allergy and Asthma Research Associates, Dallas, Texas, USA.
Allergy Asthma Proc. 2014 Sep-Oct;35(5):371-6. doi: 10.2500/aap.2014.35.3783.
Patients with hereditary angioedema (HAE) have impaired health-related quality of life (HRQoL), but the effect of preventative treatment strategies on HRQoL has not been evaluated. This study was designed to evaluate the effect of routine prevention therapy with nanofiltered C1 inhibitor (C1 INH-nf; human) on the HRQoL of patients with HAE. Thiry-six-item Short Form (SF-36) Version 1.0 questionnaires were administered at the beginning and end of two 12-week treatment periods in this multicenter, randomized, placebo-controlled, crossover study. Patients (n = 22) received intravenous injections of 1000 U of C1 INH-nf or placebo every 3-4 days for 12 weeks and then crossed over to the other treatment arm for a second 12-week period. Patients could receive open-label C1 INH-nf (1000 U) for the acute treatment of angioedema attacks in either arm of the study. Sixteen patients had evaluable SF-36 data. Mean physical component summary scores (PCSs) were 36.41 at baseline, 37.06 at the end of the placebo period, and 43.92 at the end of the C1 INH-nf period. Mean mental component summary scores (MCSs) were 49.90, 44.98, and 54.00, respectively. Least square mean differences (95% confidence intervals) between C1 INH-nf and placebo in norm-based SF-36 scores at the end of each treatment period were 6.55 (1.48, 11.62; p = 0.015) for PCS and 8.70 (1.67, 15.72; p = 0.019) for MCS. In a clinical trial setting, patients with HAE had significantly better HRQoL after 12 weeks of C1 INH-nf for routine prevention compared with acute treatment of individual angioedema attacks in the absence of routine prevention while on placebo. This study was a part of the clinical trial NCT01005888 registered in www.clinicaltrials.gov.
遗传性血管性水肿(HAE)患者的健康相关生活质量(HRQoL)受损,但预防性治疗策略对HRQoL的影响尚未得到评估。本研究旨在评估纳米过滤C1抑制剂(C1 INH-nf;人源)常规预防治疗对HAE患者HRQoL的影响。在这项多中心、随机、安慰剂对照、交叉研究的两个12周治疗期开始和结束时,使用了36项简表(SF-36)1.0版问卷。患者(n = 22)每3 - 4天接受一次1000 U C1 INH-nf或安慰剂的静脉注射,持续12周,然后交叉至另一个治疗组进行第二个12周治疗期。在研究的任一治疗组中,患者可接受开放标签的C1 INH-nf(1000 U)用于血管性水肿发作的急性治疗。16名患者有可评估的SF-36数据。平均身体成分总结得分(PCSs)在基线时为36.41,在安慰剂期结束时为37.06,在C1 INH-nf期结束时为43.92。平均心理成分总结得分(MCSs)分别为49.90、44.98和54.00。在每个治疗期结束时,基于常模的SF-36评分中,C1 INH-nf与安慰剂之间的最小二乘平均差异(95%置信区间),PCS为6.55(1.48,11.62;p = 0.015),MCS为8.70(1.67,15.72;p = 0.019)。在临床试验环境中,与在安慰剂上无常规预防措施时对个体血管性水肿发作进行急性治疗相比,HAE患者在接受12周C1 INH-nf常规预防后的HRQoL显著更好。本研究是在www.clinicaltrials.gov上注册的临床试验NCT01005888的一部分。