Real-world surveillance of standardized quality (SQ) house dust mite sublingual immunotherapy tablets for 3 years in Japan.

IF 2.6 3区 医学 Q2 ALLERGY
Minoru Gotoh, Yuriko Maekawa, Shiori Saito, Noboru Kato, Eiji Horikawa, Noriaki Nishino
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引用次数: 0

Abstract

Background: Standardized quality (SQ) house-dust mite (HDM) sublingual immunotherapy tablets (10,000 Japanese allergy units [JAU], equivalent to 6 SQ-HDM in Europe and the United States) are licensed for the treatment of HDM-induced allergic rhinitis (AR) without age restriction, based on 52-week administration clinical trials. There are no large-scale data on the administration of 10,000 JAU for > 1 year in actual clinical practice. Objective: To examine the safety and effectiveness of 10,000 JAU during use for up to 3 years at real-world clinical sites in Japan. Methods: This survey was a multicenter, observational, prospective study. We assessed the safety and effectiveness of the long-term administration of 10,000 JAU as well as effectiveness after its discontinuation in patients with HDM AR with an observation period of 3 years. Results: The safety analysis included 815 patients, and the effectiveness analysis included 768 patients. Adverse reactions that occurred in 144 patients (17.67%) were mainly site-related events that occurred early in the dosing period. Serious adverse reactions were dyspnea and anaphylactic reaction in one patient each, and both patients recovered. With regard to effectiveness, compared with scores before the administration of SQ-HDM, nasal symptom scores decreased, depending on the administration period, from 6 months to 3 years. Overall, 67.34% of the patients had improved quality of life after 6 months, and this improvement continued after 12 months. The proportion of patients with "improved and slightly improved" of overall improvement exceeded 90% after 2 years. Treatment discontinuation because "symptoms disappeared" occurred in 24.42% of the patients at 3 years. Patients who discontinued 10,000 JAU (n = 39) had a sustained improvement in nasal symptom scores compared with baseline, even 1 year after discontinuing treatment. Conclusion: The real-world safety and effectiveness of 10,000 JAU SQ-HDM sublingual immunotherapy tablets were confirmed in Japanese patients with HDM AR. No new safety and effectiveness precautions were required.

在日本对标准化质量(SQ)屋尘螨舌下免疫治疗片进行了3年的实际监测。
背景:基于52周给药临床试验,标准化质量(SQ)屋尘螨(HDM)舌下免疫治疗片(10,000日本过敏单位[JAU],相当于欧洲和美国的6 SQ-HDM)获准用于治疗HDM诱导的变应性鼻炎(AR),不受年龄限制。在实际的临床实践中,并没有10000 JAU长达100年的大规模数据。目的:在日本真实世界的临床试验中,研究10000 JAU在长达3年的使用期间的安全性和有效性。方法:本研究为多中心、观察性、前瞻性研究。我们评估了长期服用10,000 JAU的安全性和有效性,以及HDM AR患者停药后的有效性,观察期为3年。结果:安全性分析纳入815例,有效性分析纳入768例。144例(17.67%)患者的不良反应主要发生在给药期早期的部位相关事件。严重不良反应为呼吸困难、过敏反应各1例,均痊愈。在疗效方面,与给予SQ-HDM前的评分相比,根据给药时间的不同,鼻症状评分从6个月到3年不等。总体而言,67.34%的患者在6个月后生活质量得到改善,这种改善在12个月后仍在继续。2年后总体改善“改善和略改善”的患者比例超过90%。3年时,因“症状消失”而停止治疗的患者占24.42%。停止10000 JAU治疗的患者(n = 39)在停止治疗1年后,与基线相比,鼻症状评分持续改善。结论:10000 JAU SQ-HDM舌下免疫治疗片在日本HDM AR患者的实际安全性和有效性得到证实,无需新的安全性和有效性注意事项。
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来源期刊
CiteScore
5.70
自引率
35.70%
发文量
106
审稿时长
6-12 weeks
期刊介绍: Allergy & Asthma Proceedings is a peer reviewed publication dedicated to distributing timely scientific research regarding advancements in the knowledge and practice of allergy, asthma and immunology. Its primary readership consists of allergists and pulmonologists. The goal of the Proceedings is to publish articles with a predominantly clinical focus which directly impact quality of care for patients with allergic disease and asthma. Featured topics include asthma, rhinitis, sinusitis, food allergies, allergic skin diseases, diagnostic techniques, allergens, and treatment modalities. Published material includes peer-reviewed original research, clinical trials and review articles.
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