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Biomarkers as Predictors of Response to Treatment with Motesanib in Patients with Progressive Advanced Thyroid Cancer

机译:生物标志物作为进展期甲状腺癌患者对莫替沙尼治疗反应的预测指标

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Context: Antiangiogenic therapies have shown potential in the treatment of advanced thyroid cancer, but it is uncertain which patients are most likely to benefit from therapy.Objective: This prespecified exploratory analysis investigated whether baseline levels and/or changes in circulating biomarkers could predict tumor response and/or progression-free survival (PFS) among patients enrolled in a phase 2 study of motesanib in advanced thyroid cancer.Design/Setting/Patients: Patients with progressive locally advanced or metastatic medullary or differentiated thyroid cancer received motesanib 125 mg once daily for up to 48 wk in a phase 2 interventional study. Samples for assessment of circulating biomarkers of angiogenesis or apoptosis were collected at study wk 1 (baseline), 2, 4, 8, 16, 24, 32, 40, 48, and 4 wk after cessation of motesanib treatment. Tumor response was assessed per Response Evaluation Criteria in Solid Tumors by independent review.Results: Change from baseline in serum placental growth factor (PlGF) after 1 wk of treatment correlated with best tumor response (Kendall rank correlation, 0.28; P < 0.0001). Using a Fisher exact test, the most significant separation between patients who had an objective response and those who did not was at a 4.7-fold increase in PlGF. The response rate among patients with a greater than 4.7-fold increase in PlGF was 30% compared with 3% below this threshold. There was also a significant separation between responders and nonresponders at a 1.6-fold decrease in soluble vascular endothelial growth factor (VEGF) receptor 2 after 3 wk of treatment. Patients with baseline serum VEGF less than 671 pg/ml had significantly longer PFS times than the remainder of patients.Conclusions: Changes in PlGF and soluble VEGF receptor 2 levels after initiation of therapy predicted response to motesanib in patients with advanced differentiated thyroid cancer or metastatic medullary thyroid cancer. Lower baseline VEGF levels were associated with longer PFS.
机译:背景:抗血管生成疗法已显示出可治疗晚期甲状腺癌的潜力,但尚不确定哪些患者最有可能从治疗中受益。目的:这项预先确定的探索性分析调查了基线水平和/或循环生物标志物的变化是否可以预测肿瘤反应接受Motesanib晚期甲状腺癌2期研究的患者的无进展生存期(PFS)和/或无进展生存期(PFS)设计/设置/患者:进行性局部晚期或转移性髓样或分化型甲状腺癌的患者每天接受125 mg的motesanib治疗在第2阶段的介入研究中最高可达48周。在停止莫替沙尼治疗后第1、2、4、8、16、24、32、40、48和4周(基线)收集用于评估血管生成或凋亡循环生物标记物的样品。结果:在治疗1周后,血清胎盘生长因子(PlGF)从基线的变化与最佳的肿瘤反应相关(Kendall等级相关性,0.28; P <0.0001)。使用Fisher精确检验,具有客观反应的患者和没有客观反应的患者之间的最显着分离是PlGF的4.7倍增加。 PlGF增加4.7倍以上的患者的缓解率为30%,低于此阈值的3%。治疗3周后,可溶性血管内皮生长因子(VEGF)受体2降低1.6倍,应答者和非应答者之间也存在显着分离。基线血清VEGF小于671 pg / ml的患者的PFS时间明显比其余患者更长。结论:治疗开始后PlGF和可溶性VEGF受体2水平的变化预测了晚期分化型甲状腺癌或转移性患者对莫替沙尼的反应甲状腺髓样癌。较低的基线VEGF水平与较长的PFS相关。

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