Department of Medicine, Surgery and Neuroscience, Radiation Oncology Unit, University of Siena, Siena, Italy.
Radiation Oncology Unit, University of Pittsburgh Medical Center Hillman Cancer Center, San Pietro Hospital FBF, Rome, Italy.
J Neurooncol. 2020 May;148(1):47-55. doi: 10.1007/s11060-020-03442-7. Epub 2020 Feb 25.
To assess the neurocognitive function and neurological toxicity of frameless linear accelerator (LINAC)-based stereotactic radiosurgery (SRS) in patients with 10 or more brain metastases (BM).
Forty consecutive adult patients who received SRS for ten or more 10 BM < 3 cm in maximum size were evaluated. All plans were generated using a single-isocenter multiple-target (SIMT) SRS technique with doses of 22 Gy for lesions < 2 cm and 16-18 Gy for those ≥ 2 cm in size. Survival analyses were estimated by Kaplan-Meier method from the date of SRS. Neurocognitive function using the Hopkins verbal learning test-revised (HVLT-R) and activity of daily living scale (ADLS) were collected prospectively at baseline and at 3,6 and 12-month follow-up. Toxicity was assessed by the National Cancer Institute Common Toxicity Criteria for Adverse Events (Version 5.0).
With a median follow-up of 10.8 months, 1-year survival and local control rates were 65% and 86%, respectively. Grade 2 or 3 toxicity occurred in eleven patients, being associated with radiological changes suggestive of radiation necrosis in seven patients. Three months after SRS, the mean relative decline was 14.2% for HVLT-R delayed recall, 12.3% for HVLT-R recognition, and 9.8% for HVLT-R total recall. A significant deterioration of HVLT-R scores ranged from 5.5 to 18.7% of patients at different time points. ADLS scores declined over time, but changes were not significant.
SRS is an effective and safe approach for patients with 10 or more BM able to maintain the pretreatment neurocognitive function in the majority of patients.
评估 10 个或更多脑转移瘤(BM)患者接受无框架直线加速器(LINAC)立体定向放射外科(SRS)治疗后的神经认知功能和神经毒性。
对 40 例连续接受 10 个或更多最大直径<3cm 的 BM 立体定向 SRS 治疗的成年患者进行评估。所有计划均采用单等中心多靶(SIMT)SRS 技术生成,病灶<2cm 时给予 22Gy 剂量,病灶≥2cm 时给予 16-18Gy 剂量。从 SRS 日期开始,采用 Kaplan-Meier 方法进行生存分析。采用 Hopkins 言语学习测验修订版(HVLT-R)和日常生活活动量表(ADLS)进行前瞻性的神经认知功能评估,分别在基线、3、6 和 12 个月随访时采集数据。采用国立癌症研究所不良事件通用毒性标准(版本 5.0)评估毒性。
中位随访时间为 10.8 个月,1 年生存率和局部控制率分别为 65%和 86%。11 例患者出现 2 级或 3 级毒性,其中 7 例患者的影像学改变提示放射性坏死。SRS 治疗后 3 个月,HVLT-R 延迟回忆的平均相对下降率为 14.2%,HVLT-R 识别的平均相对下降率为 12.3%,HVLT-R 总回忆的平均相对下降率为 9.8%。不同时间点有 5.5%至 18.7%的患者 HVLT-R 评分显著恶化。ADLS 评分随时间下降,但变化无统计学意义。
SRS 是 10 个或更多 BM 患者的一种有效且安全的治疗方法,大多数患者可保持治疗前的神经认知功能。