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《抗 VEGF 治疗和按需治疗方案在新生血管性年龄相关性黄斑变性患者中的长期疗效:CANTREAT 研究的开放标签 12 个月扩展研究》。

Long-Term Efficacy of a Treat-and-Extend Regimen with Ranibizumab in Patients with Neovascular Age-Related Macular Disease: An Open-Label 12-Month Extension to the CANTREAT Study.

机构信息

Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario, Canada.

Ivey Eye Institute, Western University, London, Ontario, Canada.

出版信息

Ophthalmologica. 2022;245(3):230-238. doi: 10.1159/000521517. Epub 2021 Dec 30.

Abstract

INTRODUCTION

The objective of this study is to assess the long-term effectiveness of a treat-and-extend (T&E) anti-vascular endothelial growth factor regimen in patients with neovascular age-related macular degeneration who remain on T&E and those switched from once-monthly (OM) dosing to T&E (OM-T&E).

METHODS

In this 12-month extension of the 2-year CANTREAT study, patients received intravitreal ranibizumab 0.5 mg in a T&E regimen. Main outcome measures included mean change in best-corrected visual acuity (BCVA) from baseline and from month 24 to month 36; percentages of patients who gained ≥5, ≥10, or ≥15 Early Treatment of Diabetic Retinopathy Study (ETDRS) letters or lost ≥5, ≥10, or ≥15 letters from baseline and from month 24 to month 36; and number of injections administered from baseline and from month 24 to month 36 for both groups.

RESULTS

Of the 139 patients (73 T&E, 66 OM-T&E) in the extension, 121 (68 T&E, 53 OM-T&E) completed 36 months. Mean (standard deviation [SD]) BCVA changes from baseline to the extension last visit (month 33-36) were +6.6 (11.4) letters in the T&E group and +4.8 (14.3) letters in the OM-T&E group, representing maintenance of 24-month gains. The mean (SD) numbers of injections during the extension were 7.3 (2.7) for T&E and 7.1 (2.8) for OM-T&E.

DISCUSSION/CONCLUSION: These findings suggest that after 36 months of treatment, the mean BCVA improvement achieved at 24 months is maintained for both the patients exclusively treated with the T&E regimen and those that switched to T&E after 24 months in the OM regimen.

摘要

简介

本研究的目的是评估接受治疗和延长(T&E)抗血管内皮生长因子方案的患者的长期疗效,这些患者继续接受 T&E 治疗,以及从每月一次(OM)剂量转换为 T&E(OM-T&E)的患者。

方法

在这项为期 2 年的 CANTREAT 研究的 12 个月扩展研究中,患者接受玻璃体腔内雷珠单抗 0.5mg 的 T&E 方案治疗。主要观察指标包括从基线到 36 个月时最佳矫正视力(BCVA)的平均变化;从基线到 36 个月时,分别有多少患者增加了≥5、≥10 或≥15 个早期糖尿病视网膜病变治疗研究(ETDRS)字母,或丢失了≥5、≥10 或≥15 个字母;从基线到 36 个月时,两组的注射次数。

结果

在扩展研究的 139 名患者(73 名 T&E,66 名 OM-T&E)中,有 121 名(68 名 T&E,53 名 OM-T&E)完成了 36 个月的治疗。从基线到扩展最后一次就诊(第 33-36 个月)时,T&E 组的 BCVA 平均(标准差[SD])变化为+6.6(11.4)个字母,OM-T&E 组为+4.8(14.3)个字母,这表明维持了 24 个月的增益。扩展期间 T&E 组和 OM-T&E 组的平均(SD)注射次数分别为 7.3(2.7)次和 7.1(2.8)次。

讨论/结论:这些发现表明,在 36 个月的治疗后,在 24 个月时达到的平均 BCVA 改善得到维持,对于仅接受 T&E 方案治疗的患者和在 OM 方案治疗 24 个月后转换为 T&E 的患者都是如此。

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