EVEREST II研究中息肉样病变完全消退的预测因素和重要性:息肉样脉络膜血管病变中息肉消退的预测因素。

Colin S Tan, Chui Ming Gemmy Cheung, Timothy Y Y Lai, Ramune Pataluskaite, Philippe Margaron, Tock Han Lim
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引用次数: 0

摘要

目的:探讨息肉样脉络膜血管病变完全性病变(CPREG)的预测因素。方法:EVEREST ii的事后分析——一项为期24个月、多中心、随机对照的临床试验,322例息肉样脉络膜血管病变患者,随机接受雷尼单抗联合或不联合光动力治疗。吲哚菁绿血管造影(ICGA)图像由中央阅读中心分级。然后进行具有显著基线预测因子的多重逻辑回归分析,以评估第12个月CPREG的调整优势比。结果:治疗组间ICGA基线特征具有可比性。接受联合治疗的患者在M12时达到CPREG的几率更高(校正优势比= 4.64;95%置信区间2.85-7.55;P < 0.001)。在M12时,ICGA上没有息肉样病变搏动也与CPREG相关(校正优势比= 2.62;95%置信区间为1.32-5.21;P = 0.006)。M3时CPREG的存在在M12时维持CPREG的几率更高(校正优势比= 6.60;95%置信区间3.77 ~ 11.57;P < 0.001),与持续性息肉样病变相比。结论:在M12时,联合治疗比单抗治疗获得CPREG的可能性更高。这些结果有助于进一步了解息肉样病变对治疗的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PREDICTORS AND IMPORTANCE OF COMPLETE POLYPOIDAL LESION REGRESSION IN THE EVEREST II STUDY: Predictors of Polyp Regression in Polypoidal Choroidal Vasculopathy.

Purpose: To evaluate the predictors of complete polypoidal lesion regression (CPREG) in polypoidal choroidal vasculopathy.

Methods: Post hoc analysis of EVEREST II-a 24-month, multicenter, randomized, controlled clinical trial of 322 patients with polypoidal choroidal vasculopathy, randomized to receive ranibizumab with or without photodynamic therapy. Images of indocyanine green angiography (ICGA) were graded by a central reading center. Multiple logistic regression analysis with significant baseline predictors then was conducted to assess adjusted odds ratios for CPREG at month (M) 12.

Results: Baseline ICGA characteristics were comparable between the treatment groups. Patients treated with combination therapy had higher odds of achieving CPREG at M12 (adjusted odds ratio = 4.64; 95% confidence interval, 2.85-7.55; P < 0.001) compared with those in the monotherapy group. Absence of polypoidal lesion pulsation on ICGA was also associated with CPREG at M12 (adjusted odds ratio = 2.62; 95% confidence interval, 1.32-5.21; P = 0.006). The presence of CPREG at M3 had higher odds of maintaining CPREG at M12 (adjusted odds ratio = 6.60; 95% confidence interval, 3.77-11.57; P < 0.001) compared with those with persistent polypoidal lesions.

Conclusion: At M12, treatment with combination therapy was associated with higher probability of achieving CPREG than with ranibizumab monotherapy. The results contribute to the further understanding of the response of polypoidal lesions to treatment.

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