Department of Radiotherapy and Radiation Oncology, Philipps-University Marburg, Marburg, Germany.
J Neurol. 2013 Aug;260(8):2156-62. doi: 10.1007/s00415-013-6936-9. Epub 2013 May 28.
This retrospective study aimed to investigate long-term outcome in patients with arteriovenous malformations (AVM) treated with stereotactic radiosurgery (SRS). Between 1998 and 2008, 164 patients with AVM received SRS. Median age was 36 years (range 7-69 years). Before SRS, 39 % of the patients experienced haemorrhage and 27 % suffered from epileptic seizures, whereas 43 % received previously embolization, 7.9 % neurosurgery and 1.8 % proton radiotherapy. Primary SRS was applied in 51.2 % of the patients. Median single dose was 19 Gy (80 % isodose; range 18-20 Gy) and median target volume was 4 cc (range 0.1-24.4). Median follow-up was 93 months (range 12-140). Complete obliteration (CO) was observed in 100 (61 %) patients at a median time of 29 months (range 6.1-88.5). The 3 and 5-year CO rates were 61 and 88 %, respectively. In multivariate analysis, radiation dose ≥ 19 Gy (p = 0.044) and target volume <4 cc (p = 0.015) were associated with significantly higher rates of CO. Intracranial haemorrhage was seen in nine patients (5.5 %) after SRS, whereas three patients (1.8 %) died as a consequence of bleeding. The annual bleeding risk was 1.3 % after 1 year and 1.3 % after 2 years, respectively. In multivariate analysis, only target volume >4 cm(3) (p = 0.031) and Spetzler-Martin grade III-V (p = 0.046) retained significance for increased risk of intracranial bleeding. After SRS an improvement in epileptic episodes, headaches and motor-sensory deficits was found in 8.5, 14 and 15 % of patients, respectively. Our long-term follow-up data show that SRS is an effective treatment option in AVM with low toxicity and bleeding risk, depending on AVM size and Spetzler-Martin grade. An improvement of neurologic symptoms is achievable.
本回顾性研究旨在探讨接受立体定向放射外科治疗的动静脉畸形(AVM)患者的长期预后。1998 年至 2008 年间,164 例 AVM 患者接受了 SRS 治疗。中位年龄为 36 岁(7-69 岁)。SRS 前,39%的患者发生出血,27%的患者发生癫痫发作,43%的患者接受了先前的栓塞治疗,7.9%的患者接受了神经外科治疗,1.8%的患者接受了质子放疗。51.2%的患者接受了原发性 SRS。中位单次剂量为 19Gy(80%等剂量线;范围 18-20Gy),中位靶体积为 4cc(范围 0.1-24.4cc)。中位随访时间为 93 个月(12-140 个月)。100 例(61%)患者在中位时间 29 个月(6.1-88.5 个月)达到完全闭塞(CO)。3 年和 5 年 CO 率分别为 61%和 88%。多变量分析显示,剂量≥19Gy(p=0.044)和靶体积<4cc(p=0.015)与更高的 CO 率显著相关。SRS 后 9 例(5.5%)患者出现颅内出血,3 例(1.8%)患者因出血死亡。多变量分析显示,只有靶体积>4cm3(p=0.031)和 Spetzler-Martin 分级 III-V 级(p=0.046)与颅内出血风险增加相关。SRS 后,8.5%、14%和 15%的患者癫痫发作、头痛和运动感觉障碍分别得到改善。我们的长期随访数据显示,SRS 是一种有效的 AVM 治疗选择,具有低毒性和出血风险,取决于 AVM 大小和 Spetzler-Martin 分级。可改善神经症状。