符合研究性AU-011治疗条件的脉络膜黑色素瘤患者质子束照射后的结果

IF 0.9 Q4 OPHTHALMOLOGY
Frances Wu, Anne Marie Lane, Alexei Trofimov, Helen A. Shih, Evangelos S. Gragoudas, Ivana K. Kim
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引用次数: 0

摘要

& lt; b> & lt; i>简介:& lt; / i> & lt; / b>视力丧失在葡萄膜黑色素瘤放疗患者中很常见。在质子束照射(PBI)中,规定剂量的剂量在靶体积外急剧减少。然而,当肿瘤位于视神经或中央凹附近时,放射并发症很可能发生。光活化的AU-011 (belzupacap sarotalocan)是一种专门针对肿瘤细胞的研究药物,可以避免这些并发症。我们评估了符合AU-011治疗资格标准并接受PBI治疗的历史组患者的结果。& lt; b> & lt; i>方法:& lt; / i> & lt; / b>在1986年至2016年期间,在单一中心连续接受PBI治疗小脉络膜黑色素瘤的患者被确定。与AU-011临床试验的资格标准一致,当肿瘤尺寸最大厚度不超过2.5 mm,最大基底直径(LBD)不超过10.0 mm时纳入患者。Snellen视敏度转换为logMAR进行分析。对初始视力为logMAR 0.7或更高(相当于Snellen 20/100)的患者的视力结果进行分析。使用Kaplan-Meier法计算视力丧失率和死亡率。采用对数秩检验比较肿瘤位置造成的视力损失。肿瘤复发率,新生血管性青光眼(NVG)和视力丧失也被描述。& lt; b> & lt; i>结果:& lt; / i> & lt; / b>222名患者参与了这项研究。中位年龄为60.7岁(21.3-94.8岁)。中位肿瘤厚度2.0 mm(范围1.2-2.5 mm),中位LBD为8.0 mm(范围4.0-10.0 mm)。中位随访时间为6.9年(1.0-30.2年)。在204例基线logMAR视力为0.7或更高的患者中,平均基线视力为0.15(相当于Snellen 20/25), PBI后5年降至0.52(约为Snellen 20/70)。肿瘤位于视盘和/或中央窝3mm以内的患者的视力结果明显较差。肿瘤复发(1.4%)、NVG(4.5%)和视力丧失(2.7%)不常见。& lt; b> & lt; i>讨论:& lt; / i> & lt; / b>尽管质子的剂量分布有利,但超过一半位于视盘或中央凹附近的小脉络膜黑色素瘤患者在PBI后5年的视力相当于20/80或更差。AU-011治疗可以更好地保护放疗后视力丧失高风险的小肿瘤患者的视力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes after proton beam irradiation in patients with choroidal melanoma eligible for investigational AU-011 treatment
Introduction: Vision loss is common in patients treated with radiotherapy for uveal melanoma. With proton beam irradiation (PBI), the prescribed dose is delivered to the tumor with a sharp dose reduction outside the target volume. However, radiation complications are likely to develop when tumors are located near the optic nerve or fovea. Treatment with light-activated AU-011 (belzupacap sarotalocan), an investigational drug which specifically targets tumor cells, may avoid these complications. We evaluated outcomes in a historical group of patients who fit eligibility criteria for AU-011 therapy and were treated with PBI. Methods: A consecutive series of patients who received PBI for small choroidal melanoma at a single center between 1986 and 2016 were identified. Consistent with eligibility criteria in clinical trials of AU-011, patients were included when tumor dimensions did not exceed 2.5 mm in maximum thickness and 10.0 mm in largest basal diameter (LBD). Snellen visual acuities were converted to logMAR for analysis. Visual acuity outcomes were analyzed in patients with an initial acuity of logMAR 0.7 or better (equivalent to Snellen 20/100). Rates of visual acuity loss and mortality were calculated using the Kaplan-Meier method. Acuity loss by tumor location was compared using log-rank testing. Rates of tumor recurrence, neovascular glaucoma (NVG), and eye loss were also described. Results: Two hundred and 22 patients were included in the study. The median age was 60.7 years (range 21.3–94.8 years). Median tumor thickness was 2.0 mm (range 1.2–2.5 mm), and median LBD was 8.0 mm (range 4.0–10.0 mm). Median follow-up was 6.9 years (range 1.0–30.2 years). In 204 patients with a baseline logMAR visual acuity of 0.7 or better, the mean baseline acuity was 0.15 (equivalent to Snellen 20/25), which decreased to 0.52 (approximately Snellen 20/70) by 5 years after PBI. Visual outcomes were significantly worse for patients with tumors located within 3 mm of the optic disc and/or fovea. Tumor recurrence (1.4%), NVG (4.5%), and eye loss (2.7%) were uncommon. Discussion: Despite the advantageous dose distribution of protons, over half of patients with small choroidal melanomas located near the optic disc or fovea had a visual acuity equivalent to 20/80 or worse at 5 years after PBI. Treatment with AU-011 may allow better vision preservation in small tumors that carry a high risk of vision loss with radiotherapy.
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