Treatment with the SQ tree sublingual immunotherapy tablet is safe and well tolerated in real-life

IF 4.6 2区 医学 Q2 ALLERGY Clinical and Translational Allergy Pub Date : 2024-07-02 DOI:10.1002/clt2.12373
Oliver Pfaar, Hendrik Wolf, Rainer Reiber, André Knulst, Kirsten Sidenius, Mika J. Mäkelä, Sverre Steinsvåg, Christer Janson, Leonard van der Zwan, Elena Uss, Peter Arvidsson, Kathrin Borchert, Helena Himmelhaus, Eike Wüstenberg
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Abstract

Background

The SQ tree sublingual immunotherapy (SLIT)-tablet is authorised for treatment of allergic rhinoconjunctivitis with or without asthma in trees of the birch homologous group in 21 European countries. The primary objective of this study was to explore the safety in real-life.

Methods

In a prospective, non-interventional post-authorisation safety study (EUPAS31470), adverse events (AEs) and adverse drug reactions (ADRs) at first administration and follow-up visits, symptoms, medication use, and pollen food syndrome were recorded by physicians in 6 European countries during the first 4–6 months of treatment.

Results

ADRs with the SQ tree SLIT-tablet were reported in 57.7% of 1069 total patients (median age 36.0 years, 53.7% female) during the entire observation period (severity, mild-to-moderate: 70.1%, severe: 4.7%, serious: 0.7%) and in 45.9% after first administration. ADRs were not increased with pollen exposure at first administration. With coadministration of the SQ tree and grass SLIT-tablet AEs were reported in 73.8% of patients and in 52.8% with the SQ tree SLIT-tablet alone. Nasal and eye symptoms improved in 86.9% and 80.9% of patients and use of symptomatic medication in 76.0%. PFS with symptoms was reported in 43.0% of patients at baseline and in 4.3% at the individual last visit.

Conclusions

The results of this non-interventional safety study with the SQ tree SLIT-tablet confirm the safety profile from placebo-controlled clinical trials and support effectiveness in real-life according to the published efficacy data. Safety was not impaired by pollen exposure at first administration or co-administration with other SLIT-tablets.

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在现实生活中,使用 SQ 树舌下免疫疗法片剂进行治疗是安全且耐受性良好的。
背景:欧洲 21 个国家授权使用 SQ 树舌下免疫疗法(SLIT)片剂治疗伴有或不伴有哮喘的桦树同族过敏性鼻结膜炎。本研究的主要目的是探讨其在实际生活中的安全性:在一项前瞻性、非干预性的授权后安全性研究(EUPAS31470)中,欧洲 6 个国家的医生记录了首次用药和随访时的不良事件 (AE) 和药物不良反应 (ADR)、症状、用药情况和花粉食物综合征:在整个观察期内,1069 名患者中有 57.7%(中位年龄 36.0 岁,53.7% 为女性)报告了 SQ tree SLIT 片剂的 ADR(严重程度:轻度至中度:70.1%,严重:4.7%,严重:0.7%),首次用药后有 45.9%的患者报告了 ADR。首次用药后,ADR 并未随着花粉暴露量的增加而增加。73.8%的患者在同时服用SQ树和草SLIT片剂时出现了不良反应,52.8%的患者在单独服用SQ树SLIT片剂时出现了不良反应。86.9%和80.9%的患者鼻部和眼部症状有所改善,76.0%的患者使用了对症药物。43.0%的患者在基线时出现症状,4.3%的患者在最后一次就诊时出现症状:这项关于SQ tree SLIT片剂的非干预性安全性研究结果证实了安慰剂对照临床试验的安全性,并根据已公布的疗效数据支持其在现实生活中的有效性。首次给药时接触花粉或与其他 SLIT 片剂同时给药不会影响安全性。
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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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