Department of Urology, University of Munich, Klinikum Grosshadern, Munich, Germany.
BJU Int. 2011 Sep;108(5):673-8. doi: 10.1111/j.1464-410X.2010.09895.x. Epub 2010 Dec 13.
• To analyse the safety and efficacy of simultaneous standard anti-angiogenic therapy and stereotactic radiosurgery (SRS) in patients with spinal and cerebral metastases from renal cell carcinoma.
• In all, 106 patients with spinal (n= 55) or cerebral (n= 51) metastatic lesions and an Eastern Cooperative Oncology Group status of 0 or 1 were treated with sorafenib or sunitinib and simultaneous SRS. • The primary endpoint was local control. • Secondary endpoints were toxicity and overall survival.
• Median follow up was 14.7 months (range 1-42 months). Forty-five patients were treated with sunitinb and 61 patients with sorafenib. Two patients had asymptomatic tumour haemorrhage after SRS. • No skin toxicity, neurotoxicity or myelopathy occurred after SRS, and SRS did not alter the adverse effects of anti-angiogenic therapy. • Local tumour control 15 months after SRS was 98% (95% confidence interval 89-99%). The median pain score before SRS was 5 (range 1-8) and was lowered to 0 (range 0-2, P < 0.01) after SRS. There were no treatment-related deaths or late complications after SRS. • Overall survival was 17.4 months in patients with spinal lesions and 11.1 month in patients with cerebral lesions (P= 0.038).
• Simultaneous systemic anti-angiogenic therapy and SRS for selected patients with renal cell carcinoma who have spinal and cerebral metastases is safe and effective. • Single-fraction delivery allows for efficacious integration of focal radiation treatment into oncological treatment concepts without additional toxicity. • Further studies are needed to determine the limits of SRS for renal cell carcinoma metastases outside the brain and spine.
所有脊柱(n=55)或脑(n=51)转移瘤且东部肿瘤协作组(ECOG)状态为 0 或 1 的 106 例患者均接受索拉非尼或舒尼替尼治疗和 SRS 同步治疗。
主要终点为局部控制。
次要终点为毒性和总生存期。
中位随访时间为 14.7 个月(范围 1-42 个月)。45 例患者接受舒尼替尼治疗,61 例患者接受索拉非尼治疗。2 例患者 SRS 后出现无症状肿瘤出血。
SRS 后无皮肤毒性、神经毒性或脊髓病发生,SRS 也未改变抗血管生成治疗的不良反应。
SRS 后 15 个月的局部肿瘤控制率为 98%(95%置信区间 89-99%)。SRS 前疼痛评分中位数为 5(范围 1-8),SRS 后降为 0(范围 0-2,P<0.01)。SRS 后无治疗相关死亡或迟发性并发症。
脊柱病变患者的总生存期为 17.4 个月,脑病变患者为 11.1 个月(P=0.038)。
对于有脊柱和脑转移的肾细胞癌患者,选择同时进行全身抗血管生成治疗和 SRS 是安全有效的。
单次分割放疗可将有效的局部放射治疗有效地整合到肿瘤治疗方案中,而不会增加毒性。
还需要进一步的研究来确定 SRS 在脑外和脊柱外肾细胞癌转移中的应用范围。