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屋尘螨舌下含片对过敏性鼻炎患者有效且安全。

House dust mite sublingual tablet is effective and safe in patients with allergic rhinitis.

作者信息

Okamoto Y, Fujieda S, Okano M, Yoshida Y, Kakudo S, Masuyama K

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Otorhinolaryngology-Head and Neck Surgery, University of Fukui, Fukui, Japan.

出版信息

Allergy. 2017 Mar;72(3):435-443. doi: 10.1111/all.12996. Epub 2016 Aug 23.

Abstract

BACKGROUND

House dust mite (HDM) is the major indoor allergen for allergic diseases such as allergic rhinitis (AR) and asthma. Although sublingual immunotherapy is a curative treatment for HDM-induced AR, data from large-scale studies are limited. We evaluated the efficacy and safety of HDM tablets in adolescent and adult patients (aged 12-64 years) with HDM-induced AR with or without intermittent asthma.

METHODS

In a double-blind trial in Japan, 968 subjects were randomized 1 : 1 : 1 to 300 index of reactivity (IR), 500 IR, or placebo groups. The primary endpoint was the Average Adjusted Symptom Score (AASS) in the last eight weeks of the 52-week treatment. Secondary endpoints included individual nasal and ocular symptom scores, rescue medication use, and the Japanese Rhinoconjunctivitis Quality of Life Questionnaire (JRQLQ) scores.

RESULTS

The AASS in the last eight weeks of treatment significantly improved in both the 300 IR and the 500 IR groups compared to that in the placebo group (P < 0.001). In the 300 IR group, the onset of action occurred at week 8-10. All four nasal symptoms significantly improved in both active treatment groups; rescue medication use and JRQLQ outcome improved in the 300 IR group. Most adverse events (AEs) were mild, and 16 serious AEs (SAEs) were reported; however, none of them were drug-related.

CONCLUSIONS

One-year treatment with 300 IR and 500 IR HDM tablets was effective without major safety concerns. The recommended therapeutic dose for AR is 300 IR.

摘要

背景

屋尘螨(HDM)是变应性鼻炎(AR)和哮喘等过敏性疾病的主要室内变应原。尽管舌下免疫疗法是治疗HDM诱发AR的一种根治性疗法,但大规模研究的数据有限。我们评估了HDM片剂在患有或不患有间歇性哮喘的HDM诱发AR的青少年和成年患者(年龄12 - 64岁)中的疗效和安全性。

方法

在日本进行的一项双盲试验中,968名受试者按1 : 1 : 1随机分为300反应指数(IR)组、500 IR组或安慰剂组。主要终点是52周治疗最后八周的平均调整症状评分(AASS)。次要终点包括个体鼻和眼症状评分、急救药物使用情况以及日本鼻结膜炎生活质量问卷(JRQLQ)评分。

结果

与安慰剂组相比,300 IR组和500 IR组在治疗最后八周的AASS均显著改善(P < 0.001)。在300 IR组中,起效时间为第8 - 10周。两个活性治疗组的所有四种鼻症状均显著改善;300 IR组的急救药物使用情况和JRQLQ结果有所改善。大多数不良事件(AE)为轻度,报告了16例严重不良事件(SAE);然而,它们均与药物无关。

结论

300 IR和500 IR的HDM片剂进行一年治疗有效,且无重大安全问题。AR的推荐治疗剂量为300 IR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3d/5324568/d9a7fb6702d1/ALL-72-435-g001.jpg

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