Suppr超能文献

评估生物制剂治疗慢性鼻-鼻窦炎伴鼻息肉临床试验的入组和结局标准。

Evaluating enrollment and outcome criteria in trials of biologics for chronic rhinosinusitis with nasal polyps.

机构信息

Departments of Medicine and Microbiology, University of Virginia Health System, Charlottesville, Virginia.

Department of Otorhinolaryngology-Head and Neck Surgery, Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Ann Allergy Asthma Immunol. 2022 Aug;129(2):160-168. doi: 10.1016/j.anai.2022.04.004. Epub 2022 Apr 8.

Abstract

OBJECTIVE

Treatment for chronic rhinosinusitis with nasal polyps (CRSwNP) generally involves intranasal corticosteroids (INCS) and saline irrigation, followed by short courses of systemic corticosteroids (SCS) or surgery with postoperative medical therapy for patients who do not respond to INCS. However, both SCS use and surgery are associated with a range of adverse effects or complications, have a high recurrence rate, and are unsuitable for some patients. Biologics targeting the underlying pathophysiology are promising treatment alternatives for these patients. Dupilumab, omalizumab, and mepolizumab are approved for use in patients with severe, uncontrolled CRSwNP. However, the lack of a consistent definition of severe CRSwNP makes the decision to initiate biologic treatment particularly complex. Furthermore, the position of each biologic in the overall management of CRSwNP remains to be clarified.

DATA SOURCES

Publications reporting results of phase III trials of dupilumab, omalizumab, mepolizumab, and benralizumab in the treatment of CRSwNP.

STUDY SELECTIONS

Randomized, controlled phase III trials of biologics approved for CRSwNP.

RESULTS

These trials all used different enrollment criteria. We discuss the complexities of assessing CRSwNP disease severity and highlight how these impact comparisons of the populations and outcomes of the phase III biologic trials.

CONCLUSION

To position biologic agents appropriately within the existing CRSwNP treatment paradigm, future trials will need to include comparable patient populations and standardized outcome measures. Such trials will help to ensure that biologic treatment is targeted appropriately to support optimal clinical outcomes.

摘要

目的

治疗伴有鼻息肉的慢性鼻-鼻窦炎(CRSwNP)一般包括鼻内皮质类固醇(INCS)和盐水冲洗,然后对 INCS 治疗无反应的患者给予短疗程全身皮质类固醇(SCS)或手术,并在术后给予药物治疗。然而,SCS 的使用和手术都与一系列不良反应或并发症相关,且复发率较高,不适合某些患者。针对潜在病理生理学的生物制剂是这些患者有前途的治疗选择。度普利尤单抗、奥马珠单抗和美泊利珠单抗已获准用于治疗严重、控制不佳的 CRSwNP。然而,严重 CRSwNP 缺乏一致的定义,使得启动生物治疗的决策特别复杂。此外,每种生物制剂在 CRSwNP 整体管理中的地位仍有待阐明。

资料来源

报告度普利尤单抗、奥马珠单抗、美泊利珠单抗和贝那利珠单抗治疗 CRSwNP 的 III 期试验结果的出版物。

研究选择

已批准用于 CRSwNP 的生物制剂的随机、对照 III 期试验。

结果

这些试验均使用了不同的纳入标准。我们讨论了评估 CRSwNP 疾病严重程度的复杂性,并强调了这些因素如何影响 III 期生物试验人群和结果的比较。

结论

为了在现有的 CRSwNP 治疗模式中正确定位生物制剂,未来的试验需要纳入可比的患者人群和标准化的结局指标。此类试验将有助于确保生物治疗有针对性地进行,以支持最佳的临床结局。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验