Department of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Int J Radiat Oncol Biol Phys. 2013 Aug 1;86(5):873-9. doi: 10.1016/j.ijrobp.2013.04.029. Epub 2013 May 29.
Virtually all patients with malignant glioma (MG) eventually recur. This study evaluates the safety of concurrent stereotactic radiosurgery (SRS) and bevacizumab (BVZ), an antiangiogenic agent, in treatment of recurrent MG.
Fifteen patients with recurrent MG, treated at initial diagnosis with surgery and adjuvant radiation therapy/temozolomide and then at least 1 salvage chemotherapy regimen, were enrolled in this prospective trial. Lesions <3 cm in diameter were treated in a single fraction, whereas those 3 to 5 cm in diameter received 5 5-Gy fractions. BVZ was administered immediately before SRS and 2 weeks later. Neurocognitive testing (Mini-Mental Status Exam, Trail Making Test A/B), Functional Assessment of Cancer Therapy-Brain (FACT-Br) quality-of-life assessment, physical exam, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) were performed immediately before SRS and 1 week and 2 months following completion of SRS. The primary endpoint was central nervous system (CNS) toxicity. Secondary endpoints included survival, quality of life, microvascular properties as measured by DCE-MRI, steroid usage, and performance status.
One grade 3 (severe headache) and 2 grade 2 CNS toxicities were observed. No patients experienced grade 4 to 5 toxicity or intracranial hemorrhage. Neurocognition, quality of life, and Karnofsky performance status did not change significantly with treatment. DCE-MRI results suggest a significant decline in tumor perfusion and permeability 1 week after SRS and further decline by 2 months.
Treatment of recurrent MG with concurrent SRS and BVZ was not associated with excessive toxicity in this prospective trial. A randomized trial of concurrent SRS/BVZ versus conventional salvage therapy is needed to establish the efficacy of this approach.
几乎所有恶性胶质瘤(MG)患者最终都会复发。本研究评估了立体定向放射外科(SRS)联合抗血管生成药物贝伐单抗(BVZ)治疗复发性 MG 的安全性。
本前瞻性试验纳入了 15 例复发性 MG 患者,这些患者在初始诊断时接受了手术和辅助放疗/替莫唑胺治疗,然后至少接受了 1 种挽救性化疗方案。直径<3cm 的病灶接受单次分割治疗,而直径 3-5cm 的病灶接受 5 次 5Gy 分割治疗。BVZ 在 SRS 前即刻和 2 周后给予。在 SRS 前、SRS 完成后 1 周和 2 个月,进行神经认知测试(简易精神状态检查、连线测试 A/B)、癌症治疗脑功能评估量表-脑(FACT-Br)生活质量评估、体格检查和动态对比增强磁共振成像(DCE-MRI)。主要终点是中枢神经系统(CNS)毒性。次要终点包括生存、生活质量、DCE-MRI 测量的微血管特性、类固醇使用和功能状态。
观察到 1 例 3 级(严重头痛)和 2 例 2 级 CNS 毒性。无患者发生 4 级至 5 级毒性或颅内出血。神经认知、生活质量和卡氏功能状态评分在治疗后无显著变化。DCE-MRI 结果表明,SRS 后 1 周肿瘤灌注和通透性显著下降,2 个月后进一步下降。
在这项前瞻性试验中,复发性 MG 患者接受 SRS 联合 BVZ 治疗并未出现过度毒性。需要进行 SRS/BVZ 联合常规挽救性治疗的随机试验,以确定这种方法的疗效。