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基于SNOT-22的度普利尤单抗给药间隔调整对伴鼻息肉慢性鼻-鼻窦炎的治疗效果

Therapeutic Effectiveness of SNOT 22-Based Interdose Interval Adjustment of Dupilumab for Chronic Rhinosinusitis With Nasal Polyps.

作者信息

Yoon So Yeon, Cha HyunKyung, Hong Seung-No, Yang Min-Suk, Kim Dae Woo

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Catholic Kwandong University College of Medicine, Incheon, Korea.

Department of Otorhinolaryngology-Head and Neck Surgery, Soonchunhyang University Cheonan Hospital, Soonchunhyang University College of Medicine, Cheonan, Korea.

出版信息

Clin Exp Otorhinolaryngol. 2024 Nov;17(4):317-325. doi: 10.21053/ceo.2024.00233. Epub 2024 Oct 31.

Abstract

OBJECTIVES

This study evaluates the enduring efficacy and patient satisfaction of dupilumab with interdose interval adjustments based on the Sino-Nasal Outcome Test (SNOT-22) in chronic rhinosinusitis with nasal polyps (CRSwNP).

METHODS

A retrospective analysis was conducted on 44 patients who had been treated with dupilumab for over 6 months. This study targeted individuals diagnosed with CRSwNP according to the 2020 edition of the European Position Paper on Rhinosinusitis and Nasal Polyps Criteria. The treatment involved an add-on dupilumab regimen, where the interdose interval was adjusted based on the SNOT-22 scores. Dosage adjustments were made such that patients with initial SNOT-22 scores greater than 40 were tapered to a target level of 20 or less. Similarly, for patients with initial scores of 40 or less, the treatment aimed for an improvement of 50% or more. At each visit, the effectiveness of the treatment was evaluated using SNOT-22, nasal polyp scores (NPS), and a subjective satisfaction questionnaire adapted from the Treatment Satisfaction Questionnaire for Medication (TSQM v.1.4).

RESULTS

The adjustment of the interdose interval for dupilumab based on SNOT-22 scores demonstrated sustained improvements in patients' subjective symptoms, satisfaction, and NPS. The mean (standard deviation) SNOT-22 scores significantly decreased from 46.04 (22.30) to 14.72 (13.66) over 6 months (P<0.001). Similarly, NPS scores improved from 3.20 (2.24) to 1.72 (1.46) within the same period (P<0.001). Satisfaction scores, ranging from 0 to 5, consistently remained above 3.5 for up to 6 months (P=0.166). Additionally, there was a significant correlation between the improvement in the nasal symptom domain of the SNOT-22 scores and higher satisfaction scores.

CONCLUSION

Adjusting dupilumab dosing intervals based on SNOT-22 scores from the outset resulted in sustained efficacy and patient satisfaction in Korean patients with CRSwNP. This approach will meaningfully assist clinicians in determining the optimal dupilumab dosing interval.

摘要

目的

本研究评估了在伴鼻息肉的慢性鼻-鼻窦炎(CRSwNP)患者中,基于鼻-鼻窦结局测试(SNOT-22)调整度普利尤单抗给药间隔后的持久疗效及患者满意度。

方法

对44例接受度普利尤单抗治疗超过6个月的患者进行回顾性分析。本研究纳入了根据2020年版《欧洲鼻窦炎和鼻息肉立场文件》标准诊断为CRSwNP的个体。治疗采用度普利尤单抗附加治疗方案,根据SNOT-22评分调整给药间隔。进行剂量调整,使初始SNOT-22评分大于40的患者逐渐减量至目标水平20或更低。同样,对于初始评分40或更低的患者,治疗目标是改善50%或更多。每次就诊时,使用SNOT-22、鼻息肉评分(NPS)以及改编自药物治疗满意度问卷(TSQM v.1.4)的主观满意度问卷评估治疗效果。

结果

基于SNOT-22评分调整度普利尤单抗的给药间隔显示,患者的主观症状、满意度和NPS持续改善。6个月内,平均(标准差)SNOT-22评分从46.04(22.30)显著降至14.72(13.66)(P<0.001)。同样,同期NPS评分从3.20(2.24)改善至1.72(1.46)(P<0.001)。满意度评分范围为0至5,在长达6个月的时间里始终保持在3.5以上(P=0.166)。此外,SNOT-22评分的鼻部症状领域改善与更高的满意度评分之间存在显著相关性。

结论

从一开始就根据SNOT-22评分调整度普利尤单抗的给药间隔,在韩国CRSwNP患者中产生了持续疗效和患者满意度。这种方法将有效地帮助临床医生确定度普利尤单抗的最佳给药间隔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/11626100/9fdd4e4e20ce/ceo-2024-00233f1.jpg

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