Division of Oncology and Hematology, University of Nebraska Medical Center, 987680, Omaha, NE, 68198-7680, USA.
Target Oncol. 2013 Jun;8(2):117-25. doi: 10.1007/s11523-013-0254-0. Epub 2013 Jan 24.
Plasma profiling of patients treated with antiangiogenic agents may identify markers that correlate with toxicity. Objectives were to correlate changes in cytokine and angiogenic factors as potential markers of toxicity to aflibercept. Circulating cytokine and angiogenic factors were measured in 28 patients with recurrent glioblastoma in a single-arm phase II study of aflibercept. Plasma samples were analyzed at baseline, 24 h, and 28 days using multiplex assays or ELISA. We evaluated log-transformed baseline biomarker expressions with Cox proportional hazard regression models to assess the effect of markers on any grade II-IV (Gr II-IV) toxicity, on-target toxicity (hypertension, proteinuria, thromboembolism), and fatigue. All tests were two sided with a statistical significance level of p = 0.05. Among 28 pts, there were 116 Gr II-IV events. Changes in IL-13 from baseline to 24 h predicted on-target toxicities. Increases in IL-1b, IL-6, and IL-10 at 24 h were significantly associated with fatigue. Progression-free survival was 14.9 months for patients in the all-toxicity group and 9.0 months for patients in the on-target toxicity group compared to 4.3 months for those who did not develop any Gr II-IV toxicity (p = 0.002 and p = 0.045, respectively). Toxicity from antiangiogenic therapy remains an important cause of antiangiogenic treatment discontinuation and patient morbidity. Changes in IL6, IL10, and IL13 were repeatedly correlated with toxicity. Profiling of IL-13 as a surrogate for endothelial dysfunction could individualize patients at risk during antiangiogenic therapy, as could identifying those at higher risk for fatigue using IL-6 and IL-10.
接受抗血管生成药物治疗的患者的血浆分析可能可以确定与毒性相关的标志物。目的是将细胞因子和血管生成因子的变化作为潜在的毒性标志物与阿柏西普相关联。在一项阿柏西普单臂 II 期研究中,对 28 例复发性胶质母细胞瘤患者进行了循环细胞因子和血管生成因子的测量。使用多重分析或 ELISA 在基线、24 小时和 28 天分析血浆样本。我们使用对数转换的基线生物标志物表达与 Cox 比例风险回归模型进行评估,以评估标志物对任何 II-IV 级(Gr II-IV)毒性、靶毒性(高血压、蛋白尿、血栓栓塞)和疲劳的影响。所有检验均为双侧检验,统计显著性水平为 p = 0.05。在 28 例患者中,有 116 例 Gr II-IV 事件。与基线相比,24 小时时 IL-13 的变化预测靶毒性。24 小时时 IL-1b、IL-6 和 IL-10 的增加与疲劳显著相关。全毒性组患者的无进展生存期为 14.9 个月,靶毒性组患者为 9.0 个月,而未发生任何 Gr II-IV 毒性的患者为 4.3 个月(p = 0.002 和 p = 0.045)。抗血管生成治疗的毒性仍然是抗血管生成治疗中断和患者发病率的一个重要原因。IL6、IL10 和 IL13 的变化与毒性反复相关。IL-13 作为内皮功能障碍的替代物进行分析,可以个体化识别在抗血管生成治疗期间有风险的患者,也可以使用 IL-6 和 IL-10 识别那些疲劳风险更高的患者。