Reichel Felix F, Guggenberger Vanessa, Faber Hanna, Neubauer Jonas, Voykov Bogomil
University Eye Hospital, Centre for Ophthalmology, Tübingen, Baden-Württemberg, Germany.
Institute for Ophthalmic Research, Centre for Ophthalmology, Tübingen, Germany.
J Ophthalmol. 2024 Oct 26;2024:3895054. doi: 10.1155/2024/3895054. eCollection 2024.
No consensus has been reached on the adequate dose of mitomycin C (MMC) in XEN45 gel stent implantation. Lower doses have the potential to reduce MMC-linked side effects. This study aimed to evaluate treatment efficacy of ab interno XEN45 gel stent in primary open-angle glaucoma (POAG) with three different MMC doses. This retrospective single-centre nonrandomised trail included 54 patients (56 eyes) who underwent XEN45 gel stent implantation for POAG with above-target intraocular pressure (IOP) under medical therapy. Eyes were grouped according to the received MMC dose: Group 1 (20 g; = 21), Group 2 (10 g; = 14) and Group 3 (5 g; = 21). The primary endpoint was the mean IOP change in the three MMC dose groups after 6, 12 and 24 months. Secondary endpoints included the success rate defined as lowering of baseline IOP ≥ 20% and below a cut-off IOP set at three different levels: ≤ 18, ≤ 16 and ≤ 14 mmHg (Criteriums 1, 2 and 3), the mean number of ocular hypotensive medications and the frequency of needling procedures. After 24 months, the overall mean (standard error) IOP was significantly reduced from 24.7 (0.9) mmHg to 15.2 (0.7) mmHg ( < 0.0001). The average IOP change (standard error) in MMC dose groups 1, 2 and 3 was -8.6 (2) mmHg, -10.1 (2.1) mmHg and -10.4 (2.8) mmHg. Complete success (Criterium 1) was achieved in 50%, 62% and 43% of the eyes in groups 1, 2 and 3. No statistically significant difference was found within the first 24 months between the three MMC dose groups for IOP change, success rate, number of ocular hypotensive medications and the frequency of needling procedures. XE45 was effective in all three dose groups. As the success rate did not significantly differ between the MMC doses, these results may support the use of the lowest dose. ClinicalTrials.gov identifier: 559/2016BO2.
在XEN45凝胶支架植入术中,对于丝裂霉素C(MMC)的合适剂量尚未达成共识。较低剂量有可能减少与MMC相关的副作用。本研究旨在评估三种不同MMC剂量下,XEN45凝胶支架经内路植入治疗原发性开角型青光眼(POAG)的疗效。这项回顾性单中心非随机试验纳入了接受药物治疗但眼压仍高于目标值的54例(56只眼)POAG患者,他们接受了XEN45凝胶支架植入术。根据接受的MMC剂量将眼部分组:第1组(20μg;n = 21),第2组(10μg;n = 14)和第3组(5μg;n = 21)。主要终点是三个MMC剂量组在6、12和24个月后的平均眼压变化。次要终点包括成功率,定义为基线眼压降低≥20%且低于设定在三个不同水平的眼压临界值:≤18、≤16和≤14 mmHg(标准1、2和3),降眼压药物的平均数量以及针刺手术的频率。24个月后,总体平均(标准误)眼压从24.7(0.9)mmHg显著降至15.2(0.7)mmHg(P < 0.0001)。MMC剂量组1、2和3的平均眼压变化(标准误)分别为-8.6(2)mmHg、-10.1(2.1)mmHg和-10.4(2.8)mmHg。第1、2和3组分别有50%、62%和43%的眼达到完全成功(标准1)。在最初的24个月内,三个MMC剂量组在眼压变化、成功率、降眼压药物数量和针刺手术频率方面未发现统计学显著差异。XE45在所有三个剂量组中均有效。由于MMC剂量之间的成功率没有显著差异,这些结果可能支持使用最低剂量。ClinicalTrials.gov标识符:559/2016BO2。