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肿瘤内微血管密度对接受化疗联合贝伐珠单抗治疗的晚期非小细胞肺癌患者的预测价值。

Predictive value of intratumoral microvascular density in patients with advanced non-small cell lung cancer receiving chemotherapy plus bevacizumab.

机构信息

State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, People's Republic of China.

出版信息

J Thorac Oncol. 2012 Jan;7(1):71-5. doi: 10.1097/JTO.0b013e31823085f4.

Abstract

INTRODUCTION

The use of bevacizumab combined with chemotherapy represents a recent advance in clinical oncology for significantly improving the survival of patients who have non-small cell lung cancer (NSCLC). There is an unmet need for biomarkers that can predict response to such treatment and identify patients sensitive to it. Our study was designed to investigate the predictive value of intratumoral microvascular density (MVD) in patients with NSCLC treated with bevacizumab.

METHODS

Sixteen patients with NSCLC who underwent chemotherapy combined with bevacizumab were included into this study. Paraffin-embedded tumor samples were sectioned and stained immunohistochemically for the blood vessel markers CD34 and CD31 to characterize the intratumoral vasculature. A computerized image analysis program was used to quantitatively calculate the intratumoral MVD. Treatment response was evaluated by computed tomography scanning.

RESULTS

Two types of blood vessels, undifferentiated (CD31*/CD34*) and differentiated (CD34*), were identified. A positive correlation was found between the largest percentage of tumor shrinkage and the MVD of undifferentiated (CD31*/CD34*) vessels, with Spearman correlation coefficient being 0.576 (p = 0.019). No correlation between tumor shrinkage and differentiated vessel MVD (CD34*) was found. Moreover, seven of the eight patients with more undifferentiated vessels showed a partial response, versus only one of the seven patients with fewer undifferentiated vessels (p = 0.009).

CONCLUSIONS

There are two major types of microvessel in lung cancer vasculature. The MVD of undifferentiated vessels is a favorable predictor for patients with NSCLC treated with a chemotherapy regimen plus bevacizumab, with a higher MVD value correlating with better treatment response. Further studies are needed to verify the predictive role of MVD in treatment of NSCLC with bevacizumab.

摘要

简介

贝伐珠单抗联合化疗的应用是临床肿瘤学的一项重大进展,显著改善了非小细胞肺癌(NSCLC)患者的生存。目前需要寻找生物标志物来预测此类治疗的反应,并确定对其敏感的患者。我们的研究旨在探讨 NSCLC 患者接受贝伐珠单抗治疗时肿瘤内微血管密度(MVD)的预测价值。

方法

本研究纳入了 16 例接受化疗联合贝伐珠单抗治疗的 NSCLC 患者。对石蜡包埋的肿瘤样本进行免疫组织化学染色,以血管标志物 CD34 和 CD31 标记血管,以描述肿瘤内血管。使用计算机图像分析程序定量计算肿瘤内 MVD。通过计算机断层扫描评估治疗反应。

结果

鉴定出两种类型的血管,未分化(CD31*/CD34*)和分化(CD34*)。最大肿瘤退缩百分比与未分化(CD31*/CD34*)血管的 MVD 呈正相关,Spearman 相关系数为 0.576(p = 0.019)。未发现肿瘤退缩与分化血管 MVD(CD34*)之间存在相关性。此外,8 例未分化血管较多的患者中有 7 例出现部分缓解,而未分化血管较少的 7 例患者中仅有 1 例出现部分缓解(p = 0.009)。

结论

肺癌血管中有两种主要类型的微血管。未分化血管的 MVD 是接受化疗联合贝伐珠单抗治疗的 NSCLC 患者的有利预测指标,MVD 值越高,治疗反应越好。需要进一步研究以验证 MVD 在 NSCLC 贝伐珠单抗治疗中的预测作用。

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