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Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules

BACKGROUND: The use of FR + CTC to distinguish lung cancer from benign lung disease has been well studied. However, the effective method to differentiate precursor glandular lesions from benign/malignant pulmonary diseases is rare. METHODS: 380 patients with indeterminate pulmonary nodules were pros...

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Autores principales: Li, Zhixin, Cai, Jianqiao, Zhao, Yongqiang, Cai, Jie, Zhao, Xiaogang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550973/
https://www.ncbi.nlm.nih.gov/pubmed/36217263
http://dx.doi.org/10.1002/jcla.24654
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author Li, Zhixin
Cai, Jianqiao
Zhao, Yongqiang
Cai, Jie
Zhao, Xiaogang
author_facet Li, Zhixin
Cai, Jianqiao
Zhao, Yongqiang
Cai, Jie
Zhao, Xiaogang
author_sort Li, Zhixin
collection PubMed
description BACKGROUND: The use of FR + CTC to distinguish lung cancer from benign lung disease has been well studied. However, the effective method to differentiate precursor glandular lesions from benign/malignant pulmonary diseases is rare. METHODS: 380 patients with indeterminate pulmonary nodules were prospectively recruited. Peripheral blood samples were collected from all participants before surgery for analyzing FR + CTC levels. The performance of FR + CTC to identify lung precursor lesions were analyzed by receiver operating characteristic (ROC) curve. RESULTS: FR + CTC can effectively differentiate precursor from benign pulmonary diseases in all included patients (cutoff: 9.22 FU/3 ml, AUC = 0.807, (p < 0.0001, sensitivity: 69.17%, specificity: 82.46%) and patients with single pulmonary lesion (cutoff: 9.03 FU/3 ml, AUC = 0.842, p = 0.0001, sensitivity: 75.20%, specificity: 83.00%). However, FR + CTC cannot differentiate precursor from benign pulmonary diseases in multiple lesions patients (p = 0.110). FR + CTC neither differentiate precursor from malignant pulmonary lesions in all included patients (p = 0.715), single nor multiple lesions patients (p = 0.867, p = 0.692, respectively). Total number of pulmonary nodules, MTD, location (lower vs upper) were independent risk factors for malignancy (AOR, 95% CI: 3.104 (1.525, 6.316), 3.148 (1.722, 5.754), 2.098 (1.132, 3.888), respectively. CONCLUSION: Preoperative FR + CTC can be identified in precursor glandular lesions and utilized to differentiate from benign pulmonary diseases. Total number of pulmonary nodules, MTD, location (lower vs upper) were independent risk factors for malignancy.
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spelling pubmed-95509732022-10-14 Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules Li, Zhixin Cai, Jianqiao Zhao, Yongqiang Cai, Jie Zhao, Xiaogang J Clin Lab Anal Research Articles BACKGROUND: The use of FR + CTC to distinguish lung cancer from benign lung disease has been well studied. However, the effective method to differentiate precursor glandular lesions from benign/malignant pulmonary diseases is rare. METHODS: 380 patients with indeterminate pulmonary nodules were prospectively recruited. Peripheral blood samples were collected from all participants before surgery for analyzing FR + CTC levels. The performance of FR + CTC to identify lung precursor lesions were analyzed by receiver operating characteristic (ROC) curve. RESULTS: FR + CTC can effectively differentiate precursor from benign pulmonary diseases in all included patients (cutoff: 9.22 FU/3 ml, AUC = 0.807, (p < 0.0001, sensitivity: 69.17%, specificity: 82.46%) and patients with single pulmonary lesion (cutoff: 9.03 FU/3 ml, AUC = 0.842, p = 0.0001, sensitivity: 75.20%, specificity: 83.00%). However, FR + CTC cannot differentiate precursor from benign pulmonary diseases in multiple lesions patients (p = 0.110). FR + CTC neither differentiate precursor from malignant pulmonary lesions in all included patients (p = 0.715), single nor multiple lesions patients (p = 0.867, p = 0.692, respectively). Total number of pulmonary nodules, MTD, location (lower vs upper) were independent risk factors for malignancy (AOR, 95% CI: 3.104 (1.525, 6.316), 3.148 (1.722, 5.754), 2.098 (1.132, 3.888), respectively. CONCLUSION: Preoperative FR + CTC can be identified in precursor glandular lesions and utilized to differentiate from benign pulmonary diseases. Total number of pulmonary nodules, MTD, location (lower vs upper) were independent risk factors for malignancy. John Wiley and Sons Inc. 2022-08-10 /pmc/articles/PMC9550973/ /pubmed/36217263 http://dx.doi.org/10.1002/jcla.24654 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Li, Zhixin
Cai, Jianqiao
Zhao, Yongqiang
Cai, Jie
Zhao, Xiaogang
Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title_full Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title_fullStr Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title_full_unstemmed Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title_short Folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
title_sort folate receptor‐positive circulating tumor cells in the preoperative diagnosis of indeterminate pulmonary nodules
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550973/
https://www.ncbi.nlm.nih.gov/pubmed/36217263
http://dx.doi.org/10.1002/jcla.24654
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