治疗-延长方案中的最大延伸间隔和视觉结果:CANTREAT随机试验的事后分析。

IF 2.1 4区 医学 Q2 OPHTHALMOLOGY
Ophthalmologica Pub Date : 2023-01-01 DOI:10.1159/000530364
Marko M Popovic, Tom Sheidow, Jason Baker, Peter J Kertes
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引用次数: 0

摘要

加拿大兰尼单抗治疗和延长分析试验(CANTREAT)是一项为期2年的多中心随机临床试验,旨在评估兰尼单抗治疗和延长(T&E)相对于每月给药治疗新生血管性年龄相关性黄斑变性(nAMD)。这项对CANTREAT试验的事后分析探讨了接受T&E雷尼单抗的患者耐受的最大延长间隔与视力结果之间的关系。方法:Treatment-naïve nAMD患者在加拿大的27个治疗中心随机接受每月一次的雷尼单抗或T&E方案,随访24个月。在这项事后分析中,T&E队列中的患者根据最大延长间隔被细分为以下组:4周、6周、8周、10周和12周。主要结果是ETDRS最佳矫正视力(BCVA)从基线到第24个月的变化,次要结果包括视网膜中央厚度(CRT)的变化。所有结果均采用描述性统计进行报告。结果:共有285名接受T&E治疗的参与者被纳入了这项事后分析。在第24个月,4周、6周、8周、10周和12周队列中,BCVA与基线相比的变化分别为+8.5±9.3、+7.7±13.8、+4.4±9.6、+4.4±18.5和+7.8±14.8个字母。第4周、第6周、第8周、第10周和第12周,第24个月的CRT变化分别为-79.2±95.0 μm、-143.9±128.9 μm、-97.7±101.1 μm、-120.9±105.3 μm和-133.2±108.8 μm。结论:延长的能力并不一定与改善的视力结果相关,延长8-10周的BCVA变化最差。BCVA变化最大,CRT下降最低的是最长延长4周的组。其他扩展组的BCVA变化与CRT变化之间存在相关性。未来的研究应该建立nAMD患者接受T&E成功延长的预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maximal Extension Interval and Visual Outcomes in a Treat-and-Extend Protocol: A Post Hoc Analysis of the CANTREAT Randomized Trial.

Introduction: The Canadian Treat-and-Extend Analysis Trial with Ranibizumab (CANTREAT) was a 2-year, multicentred, randomized clinical trial to evaluate treat-and-extend (T&E) relative to monthly administration of ranibizumab in neovascular age-related macular degeneration (nAMD). This post hoc analysis of the CANTREAT trial explores the relationship between the maximal extension interval tolerated by patients receiving T&E ranibizumab and visual acuity outcomes.

Methods: Treatment-naïve patients with nAMD were randomized to receive either a once-monthly dosing or T&E regimen of ranibizumab across 27 treatment centres in Canada and were followed for 24 months. For this post hoc analysis, patients in the T&E cohort were subdivided into the following groups based on maximum extension interval: 4 weeks, 6 weeks, 8 weeks, 10 weeks, and 12 weeks. The primary outcome was the change in ETDRS best-corrected visual acuity (BCVA) from baseline to month 24 while secondary outcomes included change in central retinal thickness (CRT). All results were reported using descriptive statistics.

Results: A total of 285 participants undergoing T&E were enrolled in this post hoc analysis. At month 24, the change in BCVA from baseline was +8.5 ± 9.3, +7.7 ± 13.8, +4.4 ± 9.6, +4.4 ± 18.5, and +7.8 ± 14.8 letters in the 4-, 6-, 8-, 10-, and 12-week cohorts, respectively. The change in CRT at month 24 was -79.2 ± 95.0, -143.9 ± 128.9, -97.7 ± 101.1, -120.9 ± 105.3, and -133.2 ± 108.8 μm in the 4-, 6-, 8-, 10-, and 12-week cohorts, respectively.

Conclusion: The capacity to extend does not necessarily associate with improved visual acuity outcomes, with the poorest change in BCVA seen in those extended 8-10 weeks. The highest change in BCVA and lowest decrease in CRT was in the group maximally extended for 4 weeks. There was a correlation between change in BCVA and change in CRT for other extension groups. Future studies should establish the predictive factors for successful extension in patients undergoing T&E in nAMD.

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来源期刊
Ophthalmologica
Ophthalmologica 医学-眼科学
CiteScore
5.10
自引率
3.80%
发文量
39
审稿时长
3 months
期刊介绍: Published since 1899, ''Ophthalmologica'' has become a frequently cited guide to international work in clinical and experimental ophthalmology. It contains a selection of patient-oriented contributions covering the etiology of eye diseases, diagnostic techniques, and advances in medical and surgical treatment. Straightforward, factual reporting provides both interesting and useful reading. In addition to original papers, ''Ophthalmologica'' features regularly timely reviews in an effort to keep the reader well informed and updated. The large international circulation of this journal reflects its importance.
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