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Prognostic Relevance of Circulating Tumor Cells and Circulating Cell-Free DNA Association in Metastatic Non-Small Cell Lung Cancer Treated with Nivolumab

机译:尼古鲁单抗治疗转移性非小细胞肺癌中循环肿瘤细胞和循环中游离DNA缔合的预后相关性

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摘要

The treatment of advanced non-small cell lung cancer (NSCLC) has been revolutionized by immune checkpoint inhibitors (ICIs). The identification of prognostic and predictive factors in ICIs-treated patients is presently challenging. Circulating tumor cells (CTCs) and cell-free DNA (cfDNA) were evaluated in 89 previously treated NSCLC patients receiving nivolumab. Blood samples were collected before therapy and at the first and second radiological response assessments. CTCs were isolated by a filtration-based method. cfDNA was extracted from plasma and estimated by quantitative PCR. Patients with baseline CTC number and cfDNA below their median values (2 and 836.5 ng from 3 mL of blood and plasma, respectively) survived significantly longer than those with higher values (p = 0.05 and p = 0.04, respectively). The two biomarkers were then used separately and jointly as time-dependent covariates in a regression model confirming their prognostic role. Additionally, a four-fold risk of death for the subgroup presenting both circulating biomarkers above the median values was observed (p < 0.001). No significant differences were found between circulating biomarkers and best response. However, progressing patients with concomitant lower CTCs and cfDNA performed clinically well (p = 0.007), suggesting that jointed CTCs and cfDNA might help discriminate a low-risk population which might benefit from continuing ICIs beyond progression.
机译:免疫检查点抑制剂(ICIs)已彻底改变了晚期非小细胞肺癌(NSCLC)的治疗方法。在ICIs治疗的患者中确定预后和预测因素目前具有挑战性。在89名接受过nivolumab治疗的NSCLC患者中评估了循环肿瘤细胞(CTC)和无细胞DNA(cfDNA)。在治疗之前以及在第一次和第二次放射反应评估中收集血样。通过基于过滤的方法分离四氯化碳。从血浆中提取cfDNA,并通过定量PCR进行估算。基线CTC值和cfDNA低于其中值(分别来自3 mL血液和血浆的2和836.5 ng)的患者生存时间明显长于具有更高值的患者(分别为p = 0.05和p = 0.04)。然后,在回归模型中将这两个生物标志物分别用作时间依赖性协变量,以共同确认其预后作用。此外,观察到两个循环生物标志物均高于中值的亚组有四倍的死亡风险(p <0.001)。在循环生物标志物和最佳反应之间未发现显着差异。但是,伴有较低CTC和cfDNA的进展期患者在临床上表现良好(p = 0.007),这表明联合使用CTC和cfDNA可能有助于区分低危人群,这些人群可能会受益于持续发展的ICIs。

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