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Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis

AIM: This study was designed to determine the risk factors of lymph node metastasis in non‐small cell lung cancer (NSCLC) patients with tumors ≤ 2 cm, using the Shanghai Chest Hospital Lung Cancer Database. METHODS: Five hundred and eighteen patients with NSCLC ≤ 2 cm were included in this study, an...

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Autores principales: Yu, Xiyan, Li, Yanwen, Shi, Chunlei, Han, Baohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754297/
https://www.ncbi.nlm.nih.gov/pubmed/29034994
http://dx.doi.org/10.1111/1759-7714.12490
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author Yu, Xiyan
Li, Yanwen
Shi, Chunlei
Han, Baohui
author_facet Yu, Xiyan
Li, Yanwen
Shi, Chunlei
Han, Baohui
author_sort Yu, Xiyan
collection PubMed
description AIM: This study was designed to determine the risk factors of lymph node metastasis in non‐small cell lung cancer (NSCLC) patients with tumors ≤ 2 cm, using the Shanghai Chest Hospital Lung Cancer Database. METHODS: Five hundred and eighteen patients with NSCLC ≤ 2 cm were included in this study, and were classified into lymph node‐positive and lymph node‐negative groups. Univariate and multivariate logistic regression analyses were performed to select the independent risk factors for lymph node metastasis in NSCLC patients. RESULTS: No evidence of metastasis was found in tumors ≤ 1 cm, all positive results were in tumors sized 1–2 cm. Imaging characteristics, including solid and part‐solid nodules, were strongly associated with lymph node metastasis (odds ratio [OR] 24.959, 95% confidence interval [CI] 5.999–103.835, P < 0.001; OR 12.559, 95% CI 3.564–44.259, P < 0.001) and subgroup logistic analysis (OR 21.384, 95% CI 5.058–90.407, P < 0.001; OR 11.632, 95% CI 3.290–41.126, P < 0.001). Greater lymph node metastasis was observed in non‐adeno non‐squamous carcinoma. The presence of pleural invasion and carcinoembryonic antigen levels indicated lymph node dissection. Similar results were revealed in subgroup analysis in tumors ≤ 2 to > 1 cm. CONCLUSION: Size had a great impact on lymph node metastasis, especially tumors of 1–2 cm. Preoperative imaging, non‐adeno non‐squamous carcinoma, pleural invasion, and carcinoembryonic antigen all indicated lymph node dissection. There was no discrepancy between N1 and N2 positive lymph nodes.
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spelling pubmed-57542972018-01-09 Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis Yu, Xiyan Li, Yanwen Shi, Chunlei Han, Baohui Thorac Cancer Original Articles AIM: This study was designed to determine the risk factors of lymph node metastasis in non‐small cell lung cancer (NSCLC) patients with tumors ≤ 2 cm, using the Shanghai Chest Hospital Lung Cancer Database. METHODS: Five hundred and eighteen patients with NSCLC ≤ 2 cm were included in this study, and were classified into lymph node‐positive and lymph node‐negative groups. Univariate and multivariate logistic regression analyses were performed to select the independent risk factors for lymph node metastasis in NSCLC patients. RESULTS: No evidence of metastasis was found in tumors ≤ 1 cm, all positive results were in tumors sized 1–2 cm. Imaging characteristics, including solid and part‐solid nodules, were strongly associated with lymph node metastasis (odds ratio [OR] 24.959, 95% confidence interval [CI] 5.999–103.835, P < 0.001; OR 12.559, 95% CI 3.564–44.259, P < 0.001) and subgroup logistic analysis (OR 21.384, 95% CI 5.058–90.407, P < 0.001; OR 11.632, 95% CI 3.290–41.126, P < 0.001). Greater lymph node metastasis was observed in non‐adeno non‐squamous carcinoma. The presence of pleural invasion and carcinoembryonic antigen levels indicated lymph node dissection. Similar results were revealed in subgroup analysis in tumors ≤ 2 to > 1 cm. CONCLUSION: Size had a great impact on lymph node metastasis, especially tumors of 1–2 cm. Preoperative imaging, non‐adeno non‐squamous carcinoma, pleural invasion, and carcinoembryonic antigen all indicated lymph node dissection. There was no discrepancy between N1 and N2 positive lymph nodes. John Wiley & Sons Australia, Ltd 2017-10-16 2018-01 /pmc/articles/PMC5754297/ /pubmed/29034994 http://dx.doi.org/10.1111/1759-7714.12490 Text en © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Yu, Xiyan
Li, Yanwen
Shi, Chunlei
Han, Baohui
Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title_full Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title_fullStr Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title_full_unstemmed Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title_short Risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: A monocentric population‐based analysis
title_sort risk factors of lymph node metastasis in patients with non‐small cell lung cancer ≤ 2 cm in size: a monocentric population‐based analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754297/
https://www.ncbi.nlm.nih.gov/pubmed/29034994
http://dx.doi.org/10.1111/1759-7714.12490
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