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低级别颅底脑膜瘤辅助放射外科治疗后的肿瘤控制和颅神经结局。

Tumor Control and Cranial Nerve Outcomes After Adjuvant Radiosurgery for Low-Grade Skull Base Meningiomas.

机构信息

Department of Neurological Surgery and Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Department of Neurological Surgery and Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

出版信息

World Neurosurg. 2019 Jul;127:e221-e229. doi: 10.1016/j.wneu.2019.03.052. Epub 2019 Mar 14.

Abstract

OBJECTIVE

We evaluated the tumor control and cranial nerve (CN) outcomes after adjuvant stereotactic radiosurgery (SRS) for petroclival, cavernous sinus, and cerebellopontine angle meningiomas.

METHODS

From our prospectively maintained database of 2022 patients with meningioma who had undergone Leksell SRS during a 30-year interval, we found 43 patients with petroclival, 94 with cavernous sinus, and 13 patients with cerebellopontine angle meningiomas who had undergone adjuvant SRS after surgical resection of the meningioma. The patients included in the present report had had ≥1 CN deficit at the initial presentation and a minimum follow-up period of 12 months. The median age at SRS was 54 years (range, 22-81). SRS was performed for residual tumor in 104 patients (69%) and recurrent tumor in 46 patients (31%). The median tumor volume treated with SRS was 8.1 cm (range, 0.3-42), and the median margin dose was 13 Gy (range, 10-20).

RESULTS

Tumor control was achieved in 135 patients (90%) at a median follow-up point of 75 months. The progression-free survival rate after SRS was 99.5% at 1 year, 98% at 3 years, 95% at 5 years, and 90% at 10 years. Overall, 29 of the 150 patients (19%) reported improvement in CN function. Deterioration in CN function after SRS developed in 15 patients (10%). The rate of deterioration was 3.5% at 1 year, 5.5% at 3 years, and 7% at 5 years.

CONCLUSIONS

Adjuvant SRS provides effective tumor control and a low rate of new or worsening CN deficits.

摘要

目的

我们评估了立体定向放射外科(SRS)辅助治疗岩斜区、海绵窦和桥小脑角脑膜瘤的肿瘤控制和颅神经(CN)结果。

方法

从我们前瞻性维护的 2022 例脑膜瘤患者数据库中,我们发现 43 例岩斜区、94 例海绵窦和 13 例桥小脑角脑膜瘤患者在手术切除脑膜瘤后接受了辅助 SRS。本报告中包括的患者在初始表现时至少有 1 种 CN 缺陷,且随访时间至少为 12 个月。SRS 时的中位年龄为 54 岁(范围,22-81 岁)。104 例患者(69%)因残留肿瘤,46 例患者(31%)因复发性肿瘤行 SRS。SRS 治疗的中位肿瘤体积为 8.1cm(范围,0.3-42),中位边缘剂量为 13Gy(范围,10-20)。

结果

135 例患者(90%)在中位随访 75 个月时实现肿瘤控制。SRS 后 1 年、3 年、5 年和 10 年的无进展生存率分别为 99.5%、98%、95%和 90%。总体而言,150 例患者中有 29 例(19%)报告 CN 功能改善。15 例患者(10%)在 SRS 后出现 CN 功能恶化。1 年、3 年和 5 年的恶化率分别为 3.5%、5.5%和 7%。

结论

辅助 SRS 可提供有效的肿瘤控制和较低的新发或加重 CN 缺陷发生率。

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