Batchelor Tracy T, Reardon David A, de Groot John F, Wick Wolfgang, Weller Michael
Stephen E. and Catherine Pappas Center for Neuro-Oncology, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts.
Center for Neuro-Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.
Clin Cancer Res. 2014 Nov 15;20(22):5612-9. doi: 10.1158/1078-0432.CCR-14-0834.
Glioblastoma is characterized by high expression levels of proangiogenic cytokines and microvascular proliferation, highlighting the potential value of treatments targeting angiogenesis. Antiangiogenic treatment likely achieves a beneficial impact through multiple mechanisms of action. Ultimately, however, alternative proangiogenic signal transduction pathways are activated, leading to the development of resistance, even in tumors that initially respond. The identification of biomarkers or imaging parameters to predict response and to herald resistance is of high priority. Despite promising phase II clinical trial results and patient benefit in terms of clinical improvement and longer progression-free survival, an overall survival benefit has not been demonstrated in four randomized phase III trials of bevacizumab or cilengitide in newly diagnosed glioblastoma or cediranib or enzastaurin in recurrent glioblastoma. However, future studies are warranted. Predictive markers may allow appropriate patient enrichment, combination with chemotherapy may ultimately prove successful in improving overall survival, and novel agents targeting multiple proangiogenic pathways may prove effective.
胶质母细胞瘤的特征是促血管生成细胞因子的高表达水平和微血管增殖,这突出了靶向血管生成治疗的潜在价值。抗血管生成治疗可能通过多种作用机制产生有益影响。然而,最终替代的促血管生成信号转导途径会被激活,导致耐药性的产生,即使在最初有反应的肿瘤中也是如此。识别预测反应和预示耐药性的生物标志物或成像参数是当务之急。尽管贝伐单抗或西仑吉肽用于新诊断胶质母细胞瘤、或阿昔替尼或恩扎斯托林用于复发性胶质母细胞瘤的四项随机III期试验取得了有前景的II期临床试验结果且患者在临床改善和更长的无进展生存期方面受益,但尚未证明有总体生存获益。然而,未来的研究是必要的。预测性标志物可能使合适的患者得到富集,与化疗联合最终可能在改善总体生存方面取得成功,并且靶向多种促血管生成途径的新型药物可能被证明是有效的。