Suppr超能文献

用于治疗6个月至未满2岁患者眼胱氨酸病的Cystadrops眼药水

Cystadrops Eye Drops for the Management of Ocular Cystinosis in Patients Aged 6 Months to < 2 Years.

作者信息

Biswas Susmito, Casteels Ingele, Bremond-Gignac Dominique, Hogan Julien, Iarossi Giancarlo

机构信息

Manchester Royal Eye Hospital, Manchester, UK.

Department of Pediatric Ophthalmology, University Hospitals, Leuven, Belgium.

出版信息

Ophthalmol Ther. 2025 Aug 31. doi: 10.1007/s40123-025-01231-x.

Abstract

INTRODUCTION

Cystinosis is a multisystemic disease manifesting in the eyes initially as asymptomatic corneal cystine crystals and later with photophobia and serious visual impairment. Systemic effects of cystinosis arise from multiple cellular dysfunctions, causing early presymptomatic effects and progressive complications. Corneal crystals are observed across all layers of the cornea from infancy, and crystal accumulation during childhood is rapid. Early treatment is imperative, but in Europe, at the time of this study, no topical therapy was licensed for patients < 2 years of age.

METHODS

This study was a paediatric investigation plan approved by the European Medicines Agency to assess the safety profile and efficacy of Cystadrops (cysteamine hydrochloride 0.55%) over a 90-day period in patients aged 6 to < 24 months. Five patients were monitored for adverse events throughout the study. Corneal crystal score, photophobia, and best corrected visual acuity were assessed in each patient at day 1 and day 90, where possible. Compliance to Cystadrops treatment was recorded.

RESULTS

All primary endpoints were met. Any adverse events were mild and did not prevent treatment continuation. Corneal cystine crystal and photophobia scores declined or remained constant in all patients at a stage in life when an increase might be expected.

CONCLUSION

Although the rarity of the disease renders large studies on infants impracticable, there is no indication that the safety and efficacy profile of Cystadrops differs in patients above or below 2 years of age. The authors recommend treatment initiation as soon as corneal crystals are apparent.

CLINICAL TRIAL REGISTRY

Clinical Trials No: 2018-002984-24.

摘要

引言

胱氨酸病是一种多系统疾病,最初在眼部表现为无症状的角膜胱氨酸结晶,随后出现畏光和严重视力损害。胱氨酸病的全身影响源于多种细胞功能障碍,导致早期无症状影响和进行性并发症。从婴儿期开始,在角膜的所有层均可观察到角膜结晶,儿童期结晶积累迅速。早期治疗至关重要,但在欧洲,在本研究开展时,尚无适用于2岁以下患者的局部治疗方法获批。

方法

本研究是一项由欧洲药品管理局批准的儿科研究计划,旨在评估胱氨酸滴眼液(0.55%盐酸半胱胺)在6至未满24个月的患者中90天的安全性和有效性。在整个研究过程中对5名患者的不良事件进行监测。在第1天和第90天,尽可能对每位患者的角膜结晶评分、畏光情况和最佳矫正视力进行评估。记录患者对胱氨酸滴眼液治疗的依从性。

结果

所有主要终点均达成。任何不良事件均为轻度,未妨碍治疗的继续进行。在所有患者中,角膜胱氨酸结晶和畏光评分在预期会升高的生命阶段有所下降或保持不变。

结论

尽管该疾病罕见,对婴儿进行大型研究不切实际,但没有迹象表明胱氨酸滴眼液在2岁以上或以下患者中的安全性和有效性存在差异。作者建议一旦角膜结晶出现即开始治疗。

临床试验注册

临床试验编号:2018 - 002984 - 24。

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