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微血管密度对晚期 NSCLC 阿帕替尼治疗反应的预测价值。

Predictive value of microvascular density for response to anlotinib in advanced NSCLC.

机构信息

Pulmonary and Critical Care Medicine, Anqing Hospital Affiliated to Anhui Medical University, Anhui, China.

出版信息

Medicine (Baltimore). 2022 Jan 21;101(3):e28647. doi: 10.1097/MD.0000000000028647.

DOI:10.1097/MD.0000000000028647
PMID:35060554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8772671/
Abstract

Nonsmall cell lung cancer (NSCLC) is the most common type of lung cancer. This study aimed to categorize the microvessels in advanced NSCLC and determine the relationship between intratumoral microvascular density (MVD) and the efficacy of anlotinib for NSCLC.The clinical data of 68 patients receiving anlotinib as third-line treatment or beyond for advanced NSCLC were retrospectively collected. Microvessels were stained for CD31 and CD34 by using immunohistochemical staining and were classified as undifferentiated (CD31+ CD34-) and differentiated vessels (CD31+ CD34+). The relationship between MVD and anlotinib efficacy and patient prognosis was analyzed.Patients were divided into the high or low MVD groups according to the median MVD of differentiated (9.4 vessels/field) and undifferentiated microvessels (6.5 vessels/field). There were significantly more patients with high undifferentiated-vessel MVD in the disease control group than in the disease progression group (72.7% vs 16.7%, P < .001). Patients with high undifferentiated-vessel MVD had significantly longer median progression-free survival than those with low undifferentiated-vessel MVD (7.1 vs 3.7 months, P < .001).Anlotinib as third- or beyond line therapy is safe and effective for advanced NSCLC. Patients with a higher density of undifferentiated microvessels have better response to anlotinib and longer progression-free survival.

摘要

非小细胞肺癌(NSCLC)是最常见的肺癌类型。本研究旨在对晚期 NSCLC 中的微血管进行分类,并确定肿瘤内微血管密度(MVD)与安罗替尼治疗 NSCLC 疗效之间的关系。回顾性收集了 68 例接受安罗替尼三线或以上治疗的晚期 NSCLC 患者的临床资料。采用免疫组织化学染色法对 CD31 和 CD34 进行染色,并将微血管分为未分化(CD31+CD34-)和分化血管(CD31+CD34+)。分析 MVD 与安罗替尼疗效和患者预后的关系。根据分化(9.4 个/视野)和未分化微血管(6.5 个/视野)的中位 MVD 将患者分为高或低 MVD 组。疾病控制组中高未分化微血管 MVD 的患者明显多于疾病进展组(72.7%比 16.7%,P<0.001)。高未分化微血管 MVD 的患者中位无进展生存期明显长于低未分化微血管 MVD 的患者(7.1 比 3.7 个月,P<0.001)。安罗替尼作为三线或以上治疗方案,对晚期 NSCLC 安全有效。未分化微血管密度较高的患者对安罗替尼的反应更好,无进展生存期更长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/f3cc117a39ca/medi-101-e28647-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/6f56fae52724/medi-101-e28647-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/1808f7b1505f/medi-101-e28647-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/93dc8d3694c7/medi-101-e28647-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/f3cc117a39ca/medi-101-e28647-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/6f56fae52724/medi-101-e28647-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/1808f7b1505f/medi-101-e28647-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/93dc8d3694c7/medi-101-e28647-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f97/8772671/f3cc117a39ca/medi-101-e28647-g004.jpg

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