Niranjan Ajay, Raju Sudesh S, Kano Hideyuki, Flickinger John C, Lunsford Lawrence Dade
Department of Neurological Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States.
Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States.
J Neurol Surg B Skull Base. 2021 Oct;82(5):491-499. doi: 10.1055/s-0040-1714110. Epub 2020 Aug 14.
The purpose of this study was to evaluate long-term clinical outcomes and tumor control after stereotactic radiosurgery (SRS) for trigeminal schwannoma (TS). During a 28-year period (1989-2017), 50 patients underwent SRS for TS. The median patient age was 51 years (range: 15-87 years). A total of 17 patients had a previous tumor resection: 10 had a single procedure, 5 had two procedures, and 2 had three procedures. The median and mean times between tumor resection and SRS were 12 and 24 months (range: 1-90 months), respectively. Four patients had neurofibromatosis II (NF2). Based on location, tumors were classified as root type (7), ganglion type (22), or dumbbell type (21). The median radiosurgery target volume was 3.4 cm (range: 0.10-18 cm ), median target dose was 14 Gy (range: 12-20 Gy), and the median number of isocenters was 6 (range: 1-15). The median and mean times to last follow-up was 36.9 and 55.2 months (range: 4-205 months), respectively. Eighteen patients (36%) had longer than 5-year follow-up, and seven patients (14%) had longer than 10-year follow-up. The tumor control rate was 92% and the clinical improvement or stabilization rate was 94%. After SRS, the rates of progression free survival (PFS) at 1, 5, and 10 years were 98, 84, and 84%, respectively. Factors associated with improved PFS were female sex ( = 0.014) and smaller tumor volume ( = 0.022). In this series, we did not find that tumor type (root, ganglion, and dumbbell) had a statistically significant correlation to PFS. Forty-seven patients had neurological signs or symptoms at presentation. At last follow-up, neurological signs or symptoms improved in 22/47 (47%), remained unchanged in 24/50 (48%), and worsened due to tumor progression in 3/50 (6%). One patient (2%) developed temporary symptomatic adverse radiation effect (ARE) and three additional patients (6%) had transient imaging evidence of peritumoral reactive edema but no new symptoms. As a single outpatient procedure, SRS was associated with long-term freedom from additional management in 84% of patients. Nearly half the treated patients experienced improvement in neurological symptoms or signs.
本研究的目的是评估立体定向放射外科治疗(SRS)三叉神经鞘瘤(TS)后的长期临床疗效和肿瘤控制情况。在1989年至2017年的28年期间,50例患者接受了TS的SRS治疗。患者的中位年龄为51岁(范围:15 - 87岁)。共有17例患者曾接受过肿瘤切除术:10例接受过一次手术,5例接受过两次手术,2例接受过三次手术。肿瘤切除与SRS之间的中位时间和平均时间分别为12个月和24个月(范围:1 - 90个月)。4例患者患有神经纤维瘤病II型(NF2)。根据肿瘤位置,分为根部型(7例)、神经节型(22例)或哑铃型(21例)。放射外科治疗的中位靶体积为3.4 cm³(范围:0.10 - 18 cm³),中位靶剂量为14 Gy(范围:12 - 20 Gy),等中心点的中位数量为6个(范围:1 - 15个)。末次随访的中位时间和平均时间分别为36.9个月和55.2个月(范围:4 - 205个月)。18例患者(36%)随访时间超过5年,7例患者(14%)随访时间超过10年。肿瘤控制率为92%,临床改善或稳定率为94%。SRS后,1年、5年和10年的无进展生存率(PFS)分别为98%、84%和84%。与PFS改善相关的因素为女性(P = 0.014)和较小的肿瘤体积(P = 0.022)。在本系列研究中,我们未发现肿瘤类型(根部、神经节和哑铃型)与PFS有统计学显著相关性。47例患者在就诊时有神经体征或症状。在末次随访时,22/47(47%)的神经体征或症状得到改善,24/50(48%)保持不变,3/50(6%)因肿瘤进展而恶化。1例患者(2%)出现了短暂的症状性放疗不良反应(ARE),另外3例患者(6%)有肿瘤周围反应性水肿的短暂影像学证据,但无新症状。作为一种门诊单一治疗方法,SRS使84%的患者长期无需额外治疗。近一半接受治疗的患者神经症状或体征有所改善。