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Duration of skin photosensitivity and incidence of photosensitivity reactions after administration of verteporfin.

机译:施用维替泊芬后皮肤光敏持续时间和光敏反应发生率。

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BACKGROUND: Verteporfin (Visudyne, Novartis AG) is a light-activated drug that reduces the risk of vision loss in patients with certain types of choroidal neovascularization (CNV). Because photosensitivity can occur with photosensitizers, it is important for ophthalmologists providing verteporfin therapy to understand its time course and duration, as well as the incidence of photosensitivity reactions. METHODS: Data were obtained from three sources: 1) the time course of skin photosensitivity in 17 volunteers by measuring erythema/edema over time after verteporfin, using red light exposure; 2) the duration of skin photosensitivity in 30 patients with skin cancer by exposing skin to simulated solar light and calculating the daily minimal erythematous dose; and 3) the incidences of photosensitivity reactions as recorded in three phase III trials in patients with CNV secondary to age-related macular degeneration or pathologic myopia who received the regimen of verteporfin therapy currently approved by regulatory authorities (infusion of 6 mg/m(2) body surface area). RESULTS: 1) Skin photosensitivity was high at the first timepoint of 1.5 hours after dosing and decreased rapidly thereafter; 2) the duration of skin photosensitivity was dose dependent, ranging from 2.0 to 6.7 days at 6 to 20 mg/m(2), respectively (mean of 2 days at a dose of 6 mg/m(2)); and 3) photosensitivity reactions occurred in only 2.2% of patients in the phase III trials, including two severe events, one secondary to extravasation. All treatment-related reactions in the phase III trials occurred within the first 2 days after dosing, with the exception of two mild reactions and one moderate reaction that occurred 3 days after treatment. CONCLUSIONS: Verteporfin is associated with short-lived photosensitivity and a low incidence of photosensitivity reactions in clinical trials, most of which could probably have been avoided by adherence to protocol instructions for skin protection.
机译:背景:维替泊芬(Visudyne,Novartis AG)是一种光活化药物,可降低患有某些类型脉络膜新生血管(CNV)的患者视力丧失的风险。由于光敏剂会发生光敏性,因此对于提供Verteporfin治疗的眼科医生来说,了解其时间过程和持续时间以及光敏反应的发生率非常重要。方法:数据来自以下三个方面:1)17名志愿者的皮肤光敏性的时程,通过使用红光暴露测量维替泊芬后一段时间内的红斑/水肿; 2)通过将皮肤暴露于模拟太阳光下并计算每日最小红斑剂量,对30名皮肤癌患者的皮肤光敏持续时间; (3)在三期III期临床试验中,在接受监管机构批准的Verteporfin治疗方案的年龄相关性黄斑变性或病理性近视继发的CNV患者中进行的光敏反应发生率(输注6 mg / m(2 )身体表面积)。结果:1)在给药后1.5小时的第一个时间点皮肤光敏性很高,此后迅速下降。 2)皮肤光敏性的持续时间是剂量依赖性的,在6至20 mg / m(2)时分别为2.0至6.7天(在6 mg / m(2)时平均2天); (3)在III期临床试验中,仅2.2%的患者发生了光敏反应,其中包括两次严重事件,其中一项继发于外渗。 III期试验中所有与治疗相关的反应均在给药后的前2天内发生,但在治疗后3天内发生了2次轻度反应和1次中度反应。结论:Verteporfin与短暂的光敏性相关,并且在临床试验中光敏性反应的发生率较低,可以通过遵守皮肤保护规程来避免大多数此类光敏性。

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