Correlation between activated circulating endothelial cells and efficacy of anti-angiogenic therapy in non-small cell lung cancer patients

Xi-yin Wei, Jing Wang, F. Zang, Fei Zhang, Zhu-jun Liu, Cui-cui Zhang, Kai Li
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Abstract

Objective: This study aimed to examine the number of activated circulating endothelial cells (aCECs) in the peripheral blood of patients with non-small cell lung cancer (NSCLC), and investigate the relationship among aCECs, anti-angiogenic therapy, and prognosis of NSCLC patients. This study also aimed to identify novel predictive markers for anti-angiogenic therapy, and provide basic data and experimental basis for establishing an evaluation system for this therapy. Methods: A total of 142 NSCLC patients were randomly divided into the chemotherapy group (Group 1) and combined therapy group (i.e., chemotherapy plus endostatin, Group 2). The number of aCECs was measured using flow cytometry by detecting the expression status of CD105 and CD146 in the peripheral blood. The correlation between the changes in aCECs and efficacy of drug treatment was statistically analyzed using SPSS software. Results: The number of aCECs in Group 2 increased significantly at 8 and 29 d, two cycles, 50 and 71 d, and four cycles after treatment, respectively (P<0.05). In particular, aCECs amount in cases of progressive disease increased more significantly after combined therapy (P<0.05). A negative correlation was found between the treatment cycle and difference in aCECs amount before and after therapy (r= -0.970, P=0.001). A negative correlation was also observed between the difference in aCECs amount and time to tumor progression (TTP) (r=-0.351, P=0.039). Therefore, the difference in aCECs amount before and after therapy could serve as an important predictor for TTP in NSCLC patients. Conclusion: CD105 and CD146 reflected the activation status of endothelial cells, and responded to the drug treatment. Thus, CD105 and CD146 could act as ideal markers for aCECs. The number of aCECs increased during cancer progression, but significantly decreased after long-term treatment. Therefore, the change in aCECs amount may be a useful marker in predicting the efficacy of anti-angiogenic therapy.
活化循环内皮细胞与非小细胞肺癌患者抗血管生成治疗疗效的相关性
目的:本研究旨在检测非小细胞肺癌(NSCLC)患者外周血中活化循环内皮细胞(aCECs)的数量,探讨aCECs与抗血管生成治疗及NSCLC患者预后的关系。本研究旨在寻找新的抗血管生成治疗的预测标志物,为建立抗血管生成治疗的评价体系提供基础数据和实验依据。方法:142例NSCLC患者随机分为化疗组(1组)和联合治疗组(化疗+内皮抑素组,2组),通过检测外周血CD105、CD146的表达情况,采用流式细胞术检测aCECs的数量。采用SPSS软件对aCECs变化与药物治疗效果的相关性进行统计分析。结果:2组aCECs数量分别在治疗后8、29 d、2个周期、50、71 d和4个周期显著增加(P<0.05)。特别是在病情进展的情况下,联合治疗后aCECs数量增加更为显著(P<0.05)。治疗周期与治疗前后aCECs量差异呈负相关(r= -0.970, P=0.001)。aCECs量与肿瘤进展时间(TTP)的差异也呈负相关(r=-0.351, P=0.039)。因此,治疗前后aCECs量的差异可作为NSCLC患者TTP的重要预测指标。结论:CD105和CD146反映了内皮细胞的活化状态,并对药物治疗有反应。因此,CD105和CD146可以作为acec的理想标记物。aCECs数量在癌症进展过程中增加,但在长期治疗后显著减少。因此,aCECs数量的变化可能是预测抗血管生成治疗效果的有用指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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