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Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule

OBJECTIVE: To analyze multiple factors developing lung adenocarcinoma lesion from solitary pulmonary nodule (SPN). METHODS: A total of 70 patients diagnosed with lung adenocarcinoma after finding SPN by chest CT and treated in our hospital (01, 2018–01, 2021) were selected as the malignant lesion gr...

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Autores principales: Yu, Linxiang, Zhang, Bin, Zou, Haosheng, Shi, Yi, Cheng, Liang, Zhang, Ying, Zhen, Haiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9155859/
https://www.ncbi.nlm.nih.gov/pubmed/35795880
http://dx.doi.org/10.1155/2022/8330111
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author Yu, Linxiang
Zhang, Bin
Zou, Haosheng
Shi, Yi
Cheng, Liang
Zhang, Ying
Zhen, Haiwen
author_facet Yu, Linxiang
Zhang, Bin
Zou, Haosheng
Shi, Yi
Cheng, Liang
Zhang, Ying
Zhen, Haiwen
author_sort Yu, Linxiang
collection PubMed
description OBJECTIVE: To analyze multiple factors developing lung adenocarcinoma lesion from solitary pulmonary nodule (SPN). METHODS: A total of 70 patients diagnosed with lung adenocarcinoma after finding SPN by chest CT and treated in our hospital (01, 2018–01, 2021) were selected as the malignant lesion group, and another 70 patients diagnosed with benign lesion after finding SPN by CT in the same period were included in the benign lesion group. All patients had complete medical records. With univariate analysis and multivariate logistic regression, the independent risk factors for developing lung adenocarcinoma lesions from SPN were analyzed. RESULTS: By conducting univariate analysis of patients' general information (age, course of disease, BMI, nodule diameter, and gender), smoking status (smoking history and number of cigarettes smoked per year), medical history (family history of lung cancer, history of extrapulmonary malignant tumor, and history of autoimmune diseases), basic complications (hypertension and diabetes), and laboratory examinations (CEA, NSE, CYFRA21-1, SCC-Ag, and CA125), it was concluded that age, course of disease, nodule diameter, CEA positive, CYFRA21-1 positive, and CA125 positive were significantly different between the two groups (P < 0.05); the logistic regression results showed that high age, increased nodule diameter, and CYFRA21-1 positive were the independent risk factors developing lung adenocarcinoma from SPN (P < 0.05). CONCLUSION: In patients with SPN, higher age, longer course of disease, greater nodule diameter, and CYFRA21-1 positive imply increased risk for triggering lung adenocarcinoma lesion. Therefore, high attention should be paid in the clinic to such SPN patients for early diagnosis and treatment.
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spelling pubmed-91558592022-07-05 Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule Yu, Linxiang Zhang, Bin Zou, Haosheng Shi, Yi Cheng, Liang Zhang, Ying Zhen, Haiwen Contrast Media Mol Imaging Research Article OBJECTIVE: To analyze multiple factors developing lung adenocarcinoma lesion from solitary pulmonary nodule (SPN). METHODS: A total of 70 patients diagnosed with lung adenocarcinoma after finding SPN by chest CT and treated in our hospital (01, 2018–01, 2021) were selected as the malignant lesion group, and another 70 patients diagnosed with benign lesion after finding SPN by CT in the same period were included in the benign lesion group. All patients had complete medical records. With univariate analysis and multivariate logistic regression, the independent risk factors for developing lung adenocarcinoma lesions from SPN were analyzed. RESULTS: By conducting univariate analysis of patients' general information (age, course of disease, BMI, nodule diameter, and gender), smoking status (smoking history and number of cigarettes smoked per year), medical history (family history of lung cancer, history of extrapulmonary malignant tumor, and history of autoimmune diseases), basic complications (hypertension and diabetes), and laboratory examinations (CEA, NSE, CYFRA21-1, SCC-Ag, and CA125), it was concluded that age, course of disease, nodule diameter, CEA positive, CYFRA21-1 positive, and CA125 positive were significantly different between the two groups (P < 0.05); the logistic regression results showed that high age, increased nodule diameter, and CYFRA21-1 positive were the independent risk factors developing lung adenocarcinoma from SPN (P < 0.05). CONCLUSION: In patients with SPN, higher age, longer course of disease, greater nodule diameter, and CYFRA21-1 positive imply increased risk for triggering lung adenocarcinoma lesion. Therefore, high attention should be paid in the clinic to such SPN patients for early diagnosis and treatment. Hindawi 2022-05-24 /pmc/articles/PMC9155859/ /pubmed/35795880 http://dx.doi.org/10.1155/2022/8330111 Text en Copyright © 2022 Linxiang Yu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yu, Linxiang
Zhang, Bin
Zou, Haosheng
Shi, Yi
Cheng, Liang
Zhang, Ying
Zhen, Haiwen
Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title_full Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title_fullStr Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title_full_unstemmed Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title_short Multivariate Analysis on Development of Lung Adenocarcinoma Lesion from Solitary Pulmonary Nodule
title_sort multivariate analysis on development of lung adenocarcinoma lesion from solitary pulmonary nodule
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9155859/
https://www.ncbi.nlm.nih.gov/pubmed/35795880
http://dx.doi.org/10.1155/2022/8330111
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