Department of Radiation Oncology, Peking University Third Hospital, Beijing, China.
, Beijing, People's Republic of China.
Mol Cancer. 2019 Feb 7;18(1):21. doi: 10.1186/s12943-019-0950-1.
Vascular damage is followed by vascular endothelial growth factor (VEGF) expression at high levels, which is an important mechanism forradiation brain necrosis development. Bevacizumab alleviates brain edema symptoms caused by radiation brain necrosis through inhibiting VEGF and acting on vascular tissue around the brain necrosis area. Many studies have confirmed that bevacizumab effectively relieves symptoms caused by brain necrosis, improves patients' Karnofsky performance status (KPS) scores and brain necrosis imaging. However, necrosis is irreversible, and hypoxia and ischemia localized in the brain necrosis area may easily lead to radiation brain necrosis recurrence after bevacizumab is discontinued. Further studies are necessary to investigate brain necrosis diagnoses, bevacizumab indications, and the optimal mode of administration, bevacizumab resistance and necrosis with a residual or recurrent tumor.
血管损伤后会高水平表达血管内皮生长因子(VEGF),这是放射性脑坏死发展的重要机制。贝伐单抗通过抑制 VEGF 并作用于脑坏死区域周围的血管组织,缓解放射性脑坏死引起的脑水肿症状。许多研究证实,贝伐单抗能有效缓解脑坏死引起的症状,改善患者的卡诺夫斯基表现状态(KPS)评分和脑坏死影像学表现。然而,坏死是不可逆的,脑坏死区域的局部缺氧和缺血很容易导致贝伐单抗停药后放射性脑坏死复发。需要进一步研究来探讨脑坏死的诊断、贝伐单抗的适应证、最佳给药方式、贝伐单抗耐药性以及伴有残留或复发肿瘤的坏死。