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Prognostic significance of circulating tumor cells in non-small cell lung cancer patients undergoing chemotherapy

机译:非小细胞肺癌化疗患者循环肿瘤细胞的预后意义

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摘要

The utility of circulating tumor cells (CTCs) as prognostic biomarkers in non-small cell lung cancer (NSCLC) is inconclusive due to the limitations of current CTC detection methods. Using a novel high-efficiency detection method, we determined the ability of CTCs to predict survival and chemotherapeutic responses in NSCLC. In 127 patients with advanced NSCLC, CTCs were counted and analyzed at baseline and during follow-up. Median overall survival (OS) and progression-free survival (PFS) were longer in patients with baseline CTC counts <8 CTCs/3.2 mL (20.0 vs. 10.4 months [P = 0.009] and 7.2 vs. 5.5 months [P < 0.001], respectively). Patients with post-treatment increases in the CTC count had poorer OS and PFS than those without increases (12.0 vs. 13.3 months [P = 0.028] and 5.2 vs. 6.4 months [P = 0.022], respectively). There was no association between the baseline CTC count and chemotherapeutic response (P = 0.734). However, the rate of progressive disease in patients with and without post-treatment increases in the CTC count were 15.6% and 2.4% (P = 0.042), respectively. The baseline CTC count and the change in the CTC count during treatment were both valuable prognostic indicators for NSCLC.
机译:由于当前CTC检测方法的局限性,循环肿瘤细胞(CTC)在非小细胞肺癌(NSCLC)中作为预后生物标志物的用途尚无定论。使用新颖的高效检测方法,我们确定了CTC预测NSCLC存活和化疗反应的能力。在127例晚期NSCLC患者中,在基线和随访期间对CTC进行了计数和分析。基线CTC计数<8 CTC / 3.2 mL的患者中位总生存期(OS)和无进展生存期(PFS)更长(20.0 vs. 10.4个月[P = 0.009]和7.2 vs. 5.5个月[P <0.001] , 分别)。治疗后CTC计数增加的患者的OS和PFS较未升高的患者差(分别为12.0 vs. 13.3个月[P = 0.028]和5.2 vs. 6.4 mo [P = 0.022])。基线CTC计数与化疗反应之间没有关联(P = 0.734)。但是,在有或没有治疗后CTC计数增加的患者中,进行性疾病的发生率分别为15.6%和2.4%(P = 0.042)。基线CTC计数和治疗期间CTC计数的变化都是NSCLC有价值的预后指标。

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