Departments of 1 Otolaryngology-Head and Neck Surgery.
Neurologic Surgery, and.
J Neurosurg. 2017 Aug;127(2):380-387. doi: 10.3171/2016.5.JNS153013. Epub 2016 Nov 25.
OBJECTIVE Over the last 30 years, stereotactic radiosurgery (SRS) has become an established noninvasive treatment alternative for small- to medium-sized vestibular schwannoma (VS). This study aims to further define long-term SRS tumor control in patients with documented pretreatment tumor growth for whom conservative observation failed. METHODS A prospective clinical database was queried, and patients with sporadic VS who elected initial observation and subsequently underwent SRS after documented tumor growth between 2004 and 2014 were identified. Posttreatment tumor growth or shrinkage was determined by a ≥ 2-mm increase or decrease in maximum linear dimension, respectively. RESULTS Sixty-eight patients met study inclusion criteria. The median pre- and posttreatment observation periods were 16 and 43.5 months, respectively. The median dose to the tumor margin was 13 Gy (range 12-14 Gy), and the median maximum dose was 26 Gy (range 24-28 Gy). At the time of treatment, 59 tumors exhibited extracanalicular (EC) extension, and 9 were intracanalicular (IC). Of the 59 EC VSs, 50 (85%) remained stable or decreased in size following treatment, and 9 (15%) enlarged by > 2 mm. Among EC tumors, the median pretreatment tumor growth rate was 2.08 mm/year for tumors that decreased or were stable, compared with 3.26 mm/year for tumors that grew following SRS (p = 0.009). Patients who demonstrated a pretreatment growth rate of < 2.5 mm/year exhibited a 97% tumor control rate, compared with 69% for those demonstrating ≥ 2.5 mm/year of growth prior to SRS (p = 0.007). No other analyzed variables were found to predict tumor growth following SRS. CONCLUSIONS Overall, SRS administered using a marginal dose between 12-14 Gy is highly effective in treating VSs in which initial observation fails. Tumor control is achieved in 97% of VSs that exhibit slow (< 2.5 mm/year) pretreatment growth; however, SRS is less successful in treating tumors exhibiting rapid growth (≥ 2.5 mm/year).
在过去的 30 年中,立体定向放射外科(SRS)已成为治疗小至中型前庭神经鞘瘤(VS)的一种成熟的非侵入性治疗选择。本研究旨在进一步确定对保守观察失败后出现记录的肿瘤生长的患者进行 SRS 治疗的长期肿瘤控制情况。
对前瞻性临床数据库进行了查询,并确定了 2004 年至 2014 年期间因记录的肿瘤生长而选择初始观察并随后接受 SRS 治疗的散发性 VS 患者。通过最大线性尺寸分别增加或减少≥2mm 来确定治疗后的肿瘤生长或缩小。
68 名患者符合研究纳入标准。治疗前和治疗后的中位观察期分别为 16 个月和 43.5 个月。肿瘤边缘的中位剂量为 13Gy(范围为 12-14Gy),最大剂量的中位数为 26Gy(范围为 24-28Gy)。在治疗时,59 个肿瘤有管外(EC)延伸,9 个是管内(IC)。在 59 个 EC VS 中,50 个(85%)在治疗后保持稳定或缩小,9 个(15%)增大> 2mm。在 EC 肿瘤中,与 SRS 后生长的肿瘤相比,缩小或稳定的肿瘤的中位预处理肿瘤生长速度为 2.08mm/年,而生长的肿瘤的生长速度为 3.26mm/年(p = 0.009)。显示预处理生长速度<2.5mm/年的患者肿瘤控制率为 97%,而 SRS 前生长速度≥2.5mm/年的患者为 69%(p = 0.007)。未发现其他分析变量可预测 SRS 后的肿瘤生长。
总体而言,使用 12-14Gy 之间的边缘剂量进行 SRS 治疗,对于初始观察失败的 VS 非常有效。在显示出缓慢(<2.5mm/年)预处理生长的 97%VS 中实现了肿瘤控制;但是,SRS 在治疗生长迅速(≥2.5mm/年)的肿瘤方面效果较差。