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Predictive value of microvascular density for response to anlotinib in advanced NSCLC
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 receiv...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772671/ https://www.ncbi.nlm.nih.gov/pubmed/35060554 http://dx.doi.org/10.1097/MD.0000000000028647 |
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author | Liu, Danqing Ding, Guozheng |
author_facet | Liu, Danqing Ding, Guozheng |
author_sort | Liu, Danqing |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8772671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-87726712022-01-21 Predictive value of microvascular density for response to anlotinib in advanced NSCLC Liu, Danqing Ding, Guozheng Medicine (Baltimore) 5700 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. Lippincott Williams & Wilkins 2022-01-21 /pmc/articles/PMC8772671/ /pubmed/35060554 http://dx.doi.org/10.1097/MD.0000000000028647 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 5700 Liu, Danqing Ding, Guozheng Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title | Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title_full | Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title_fullStr | Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title_full_unstemmed | Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title_short | Predictive value of microvascular density for response to anlotinib in advanced NSCLC |
title_sort | predictive value of microvascular density for response to anlotinib in advanced nsclc |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772671/ https://www.ncbi.nlm.nih.gov/pubmed/35060554 http://dx.doi.org/10.1097/MD.0000000000028647 |
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