The Christie NHS Foundation Trust and Division of Cancer Sciences, University of Manchester, Manchester, M20 4BX, UK.
Division of Cancer Sciences, Manchester Cancer Research Centre, University of Manchester, Manchester, M20 4GJ, UK.
Nat Commun. 2018 Nov 7;9(1):4672. doi: 10.1038/s41467-018-07174-1.
Oncological use of anti-angiogenic VEGF inhibitors has been limited by the lack of informative biomarkers. Previously we reported circulating Tie2 as a vascular response biomarker for bevacizumab-treated ovarian cancer patients. Using advanced MRI and circulating biomarkers we have extended these findings in metastatic colorectal cancer (n = 70). Bevacizumab (10 mg/kg) was administered to elicit a biomarker response, followed by FOLFOX6-bevacizumab until disease progression. Bevacizumab induced a correlation between Tie2 and the tumor vascular imaging biomarker, K (R:-0.21 to 0.47) implying that Tie2 originated from the tumor vasculature. Tie2 trajectories were independently associated with pre-treatment tumor vascular characteristics, tumor response, progression free survival (HR for progression = 3.01, p = 0.00014; median PFS 248 vs. 348 days p = 0.0008) and the modeling of progressive disease (p < 0.0001), suggesting that Tie2 should be monitored clinically to optimize VEGF inhibitor use. A vascular response is defined as a 30% reduction in Tie2; vascular progression as a 40% increase in Tie2 above the nadir. Tie2 is the first, validated, tumor vascular response biomarker for VEGFi.
抗血管生成 VEGF 抑制剂的肿瘤学应用受到缺乏信息性生物标志物的限制。我们之前曾报道过循环 Tie2 是贝伐珠单抗治疗卵巢癌患者的血管反应生物标志物。我们使用先进的 MRI 和循环生物标志物,将这些发现扩展到转移性结直肠癌患者中(n=70)。给予贝伐珠单抗(10mg/kg)以引起生物标志物反应,然后给予 FOLFOX6-贝伐珠单抗直至疾病进展。贝伐珠单抗诱导 Tie2 与肿瘤血管成像生物标志物 K(R:-0.21 至 0.47)之间的相关性,表明 Tie2 来源于肿瘤血管。Tie2 轨迹与治疗前肿瘤血管特征、肿瘤反应、无进展生存期(进展的 HR=3.01,p=0.00014;中位 PFS 248 与 348 天,p=0.0008)和进行性疾病的建模独立相关,这表明应临床监测 Tie2 以优化 VEGF 抑制剂的使用。血管反应定义为 Tie2 减少 30%;血管进展定义为 Tie2 比最低点增加 40%。Tie2 是第一个经过验证的 VEGFi 肿瘤血管反应生物标志物。