Department of Neurosurgery, University of Virginia, Charlottesville, Virginia.
Gamma Knife Center Cairo, Nasser Institute Hospital, Cairo, Egypt.
Neurosurgery. 2021 Mar 15;88(4):828-837. doi: 10.1093/neuros/nyaa544.
Stereotactic radiosurgery (SRS) is increasingly used for management of perioptic meningiomas.
To study the safety and effectiveness of SRS for perioptic meningiomas.
From 12 institutions participating in the International Radiosurgery Research Foundation (IRRF), we retrospectively assessed treatment parameters and outcomes following SRS for meningiomas located within 3 mm of the optic apparatus.
A total of 438 patients (median age 51 yr) underwent SRS for histologically confirmed (29%) or radiologically suspected (71%) perioptic meningiomas. Median treatment volume was 8.01 cm3. Median prescription dose was 12 Gy, and median dose to the optic apparatus was 8.50 Gy. A total of 405 patients (93%) underwent single-fraction SRS and 33 patients (7%) underwent hypofractionated SRS. During median imaging follow-up of 55.6 mo (range: 3.15-239 mo), 33 (8%) patients experienced tumor progression. Actuarial 5-yr and 10-yr progression-free survival was 96% and 89%, respectively. Prescription dose of ≥12 Gy (HR: 0.310; 95% CI [0.141-0.679], P = .003) and single-fraction SRS (HR: 0.078; 95% CI [0.016-0.395], P = .002) were associated with improved tumor control. A total of 31 (10%) patients experienced visual decline, with actuarial 5-yr and 10-yr post-SRS visual decline rates of 9% and 21%, respectively. Maximum dose to the optic apparatus ≥10 Gy (HR = 2.370; 95% CI [1.086-5.172], P = .03) and tumor progression (HR = 4.340; 95% CI [2.070-9.097], P < .001) were independent predictors of post-SRS visual decline.
SRS provides durable tumor control and quite acceptable rates of vision preservation in perioptic meningiomas. Margin dose of ≥12 Gy is associated with improved tumor control, while a dose to the optic apparatus of ≥10 Gy and tumor progression are associated with post-SRS visual decline.
立体定向放射外科(SRS)越来越多地用于眶内脑膜瘤的治疗。
研究 SRS 治疗眶内脑膜瘤的安全性和有效性。
从参与国际放射外科研究基金会(IRRF)的 12 个机构中,我们回顾性评估了 SRS 治疗位于视神经装置 3 毫米以内的脑膜瘤的治疗参数和结果。
共有 438 名患者(中位年龄 51 岁)接受了 SRS 治疗,组织学证实(29%)或影像学怀疑(71%)为眶内脑膜瘤。中位治疗体积为 8.01cm³。中位处方剂量为 12Gy,视神经剂量中位数为 8.50Gy。405 名患者(93%)接受单次 SRS 治疗,33 名患者(7%)接受分次 SRS 治疗。在中位影像学随访 55.6 个月(范围:3.15-239 个月)期间,33 名患者(8%)发生肿瘤进展。5 年和 10 年无进展生存率分别为 96%和 89%。处方剂量≥12Gy(HR:0.310;95%CI [0.141-0.679],P=0.003)和单次 SRS(HR:0.078;95%CI [0.016-0.395],P=0.002)与肿瘤控制改善相关。共有 31 名患者(10%)出现视力下降,SRS 后 5 年和 10 年的视力下降发生率分别为 9%和 21%。视神经最高剂量≥10Gy(HR=2.370;95%CI [1.086-5.172],P=0.03)和肿瘤进展(HR=4.340;95%CI [2.070-9.097],P<.001)是 SRS 后视力下降的独立预测因素。
SRS 为眶内脑膜瘤提供了持久的肿瘤控制和相当可接受的视力保留率。边缘剂量≥12Gy 与肿瘤控制改善相关,而视神经剂量≥10Gy 和肿瘤进展与 SRS 后视力下降相关。