Department of Radiation Oncology, Stanford University Medical Center, Stanford, CA 94305-5847, USA.
Int J Radiat Oncol Biol Phys. 2011 May 1;80(1):213-20. doi: 10.1016/j.ijrobp.2010.01.040.
To evaluate spinal cord dose-volume effects, we present a retrospective review of stereotactic radiosurgery (SRS) treatments for spinal cord hemangioblastomas.
From November 2001 to July 2008, 27 spinal hemangioblastomas were treated in 19 patients with SRS. Seventeen tumors received a single fraction with a median dose of 20 Gy (range, 18-30 Gy). Ten lesions were treated using 18-25 Gy in two to three sessions. Cord volumes receiving 8, 10, 12, 14, 16, 18, 20, 22, and 24 Gy and dose to 10, 100, 250, 500, 1000, and 2000 mm(3) of cord were determined. Multisession treatments were converted to single-fraction biologically effective dose (SFBED).
Single-fraction median cord D(max) was 22.7 Gy (range, 17.8-30.9 Gy). Median V10 was 454 mm(3) (range, 226-3543 mm(3)). Median dose to 500 mm(3) cord was 9.5 Gy (range, 5.3-22.5 Gy). Fractionated median SFBED(3) cord D(max) was 14.1 Gy(3) (range, 12.3-19.4 Gy(3)). Potential toxicities included a Grade 2 unilateral foot drop 5 months after SRS and 2 cases of Grade 1 sensory deficits. The actuarial 3-year local tumor control estimate was 86%.
Despite exceeding commonly cited spinal cord dose constraints, SRS for spinal hemangioblastomas is safe and effective. Consistent with animal experiments, these data support a partial-volume tolerance model for the human spinal cord. Because irradiated cord volumes were generally small, application of these data to other clinical scenarios should be made cautiously. Further prospective studies of spinal radiosurgery are needed.
为了评估脊髓剂量-体积效应,我们回顾性分析了立体定向放射外科(SRS)治疗脊髓血管母细胞瘤的疗效。
从 2001 年 11 月至 2008 年 7 月,19 例患者的 27 个脊髓血管母细胞瘤接受了 SRS 治疗。17 个肿瘤接受了单次分割治疗,中位剂量为 20 Gy(范围 18-30 Gy)。10 个病变采用 18-25 Gy 的剂量进行 2-3 次分割治疗。确定脊髓接受 8、10、12、14、16、18、20、22 和 24 Gy 及剂量为 10、100、250、500、1000 和 2000 mm(3)的脊髓体积。多分割治疗转化为单次分割生物有效剂量(SFBED)。
单次分割中位脊髓 D(max)为 22.7 Gy(范围 17.8-30.9 Gy)。中位 V10 为 454 mm(3)(范围 226-3543 mm(3))。中位 500 mm(3)脊髓剂量为 9.5 Gy(范围 5.3-22.5 Gy)。分次中位 SFBED(3)脊髓 D(max)为 14.1 Gy(3)(范围 12.3-19.4 Gy(3))。潜在的毒性包括 SRS 后 5 个月出现的 2 级单侧足下垂和 2 例 1 级感觉缺陷。3 年局部肿瘤控制率估计为 86%。
尽管脊髓剂量超过了常见的限制,但 SRS 治疗脊髓血管母细胞瘤是安全有效的。与动物实验一致,这些数据支持人类脊髓的部分体积耐受模型。由于受照射脊髓体积通常较小,应谨慎将这些数据应用于其他临床情况。需要进一步进行前瞻性的脊髓放射外科研究。