Therapeutic Effectiveness SNOT 22-based interdose interval adjustment of dupilumab for CRSwNP.

IF 2.9 3区 医学 Q1 OTORHINOLARYNGOLOGY Clinical and Experimental Otorhinolaryngology Pub Date : 2024-10-31 DOI:10.21053/ceo.2024.00233
So Yeon Yoon, HyunKyung Cha, Seung-No Hong, Min-Suk Yang, Dae Woo Kim
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Abstract

Objectives: This study aims to evaluate whether Sino-nasal Outcome Test (SNOT-22)-based interdose interval adjustment of dupilumab demonstrates enduring efficacy and patient satisfaction in chronic rhinosinusitis with nasal polyps (CRSwNP).

Methods: A retrospective analysis was conducted using planned data collection from 44 patients who received dupilumab and had been followed up for more than 6 months, targeting individuals with CRSwNP based on the EPOS 2020 Criteria. Patients were treated with add-on dupilumab by adjusting the interdose interval based on SNOT-22, which was tapered when subjects with >40 SNOT-22 at pretreatment evaluation were controlled at the level of ≤20 SNOT-22; when subjects with ≤40 SNOT-22 at pretreatment evaluation were controlled at the level of ≥50% improvement. SNOT-22, nasal polyp scores (NPS), and a subjective satisfaction questionnaire modified from the Treatment Satisfaction Questionnaire for Medication (TSQM v.1.4) were assessed at each visit.

Results: The SNOT-22-based interdose interval adjustment of dupilumab showed sustained improvement in patients' subjective symptoms, satisfaction, and NPS. Mean scores (S.D) of SNOT-22 improved from 46.04 (22.30) to 14.72 (13.66) at 6 months (p=0.000); NPS improved from 3.20 (2.24) to 1.72 (1.46) at 6 months (p=0.000). Satisfaction scores (0-5) were well maintained above 3.5 points for up to 6 months(p=0.166). There was also a significant correlation between the improvement in the nasal symptom domain of SNOT-22 scores and higher satisfaction scores.

Conclusion: Adjusting dupilumab intervals based on SNOT-22 from the start leads to sustained efficacy and patient satisfaction in Korean CRSwNP. This will be of great clinical help in determining the optimal dupilumab interval.

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基于疗效 SNOT 22,调整杜必鲁单抗治疗 CRSwNP 的用药间隔。
研究目的本研究旨在评估基于SNOT-22结果测试(Sino-nasal Outcome Test)的dupilumab剂量间隔调整是否对伴有鼻息肉的慢性鼻炎(CRSwNP)具有持久疗效和患者满意度:根据EPOS 2020标准,针对CRSwNP患者进行了一项回顾性分析,计划收集44名接受过杜比单抗治疗且随访时间超过6个月的患者的数据。根据SNOT-22调整两次给药的间隔时间,当患者在治疗前评估时SNOT-22大于40,而治疗后SNOT-22控制在≤20的水平时,则减量给药;当患者在治疗前评估时SNOT-22≤40,而治疗后SNOT-22控制在改善≥50%的水平时,则减量给药。每次就诊时评估 SNOT-22、鼻息肉评分(NPS)和根据药物治疗满意度问卷(TSQM v.1.4)修改的主观满意度问卷:结果:基于 SNOT-22 的双鲁单抗剂量间隔调整显示,患者的主观症状、满意度和 NPS 均有持续改善。SNOT-22 的平均得分(S.D)从 46.04(22.30)分改善到 6 个月时的 14.72(13.66)分(P=0.000);NPS 从 3.20(2.24)分改善到 6 个月时的 1.72(1.46)分(P=0.000)。满意度评分(0-5 分)在 6 个月内一直保持在 3.5 分以上(p=0.166)。SNOT-22评分中鼻腔症状领域的改善与较高的满意度评分之间也存在明显的相关性:结论:在韩国 CRSwNP 患者中,从一开始就根据 SNOT-22 调整杜必鲁单抗的间隔时间可获得持续疗效和患者满意度。结论:根据 SNOT-22 从一开始就对韩国 CRSwNP 患者的疗效和满意度进行调整,可使疗效和满意度保持稳定,这对确定杜比鲁单抗的最佳治疗间隔有很大临床帮助。
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来源期刊
CiteScore
4.90
自引率
6.70%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Clinical and Experimental Otorhinolaryngology (Clin Exp Otorhinolaryngol, CEO) is an international peer-reviewed journal on recent developments in diagnosis and treatment of otorhinolaryngology-head and neck surgery and dedicated to the advancement of patient care in ear, nose, throat, head, and neck disorders. This journal publishes original articles relating to both clinical and basic researches, reviews, and clinical trials, encompassing the whole topics of otorhinolaryngology-head and neck surgery. CEO was first issued in 2008 and this journal is published in English four times (the last day of February, May, August, and November) per year by the Korean Society of Otorhinolaryngology-Head and Neck Surgery. The Journal aims at publishing evidence-based, scientifically written articles from different disciplines of otorhinolaryngology field. The readership contains clinical/basic research into current practice in otorhinolaryngology, audiology, speech pathology, head and neck oncology, plastic and reconstructive surgery. The readers are otolaryngologists, head and neck surgeons and oncologists, audiologists, and speech pathologists.
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