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Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer

OBJECTIVE: In this cohort study, we determined the clinical value of the maximum standardized uptake value (SUVmax) of primary tumors in non‐small cell lung cancer (NSCLC). STUDY DESIGN: A retrospective review of NSCLC patients was performed from January 2011 to December 2017. Peripheral cN0 NSCLC p...

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Autores principales: Wang, Shuai, Lin, Dong, Yang, Xiaodong, Zhan, Cheng, Zhao, Shihai, Luo, Rongkui, Wang, Qun, Tan, Lijie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131855/
https://www.ncbi.nlm.nih.gov/pubmed/32056387
http://dx.doi.org/10.1002/cam4.2900
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author Wang, Shuai
Lin, Dong
Yang, Xiaodong
Zhan, Cheng
Zhao, Shihai
Luo, Rongkui
Wang, Qun
Tan, Lijie
author_facet Wang, Shuai
Lin, Dong
Yang, Xiaodong
Zhan, Cheng
Zhao, Shihai
Luo, Rongkui
Wang, Qun
Tan, Lijie
author_sort Wang, Shuai
collection PubMed
description OBJECTIVE: In this cohort study, we determined the clinical value of the maximum standardized uptake value (SUVmax) of primary tumors in non‐small cell lung cancer (NSCLC). STUDY DESIGN: A retrospective review of NSCLC patients was performed from January 2011 to December 2017. Peripheral cN0 NSCLC patients with tumor size ≤2 cm were included. SUVmax was calculated as a continuous variable for semiquantitative analyses. A receiver operating characteristic curve was analyzed to assess the cutoff threshold of SUVmax on pathological (p) nodal metastasis. We further evaluated the clinical relevance of SUVmax in peripheral cN0 NSCLC patients. RESULTS: A total of 670 peripheral NSCLC patients with tumor size ≤2 cm were deemed cN0 by preoperative PET/CT scan. Statistical analyses suggested significant correlations of SUVmax with smoking status (P = .026), tumor volume (P = .001), pathology type (P = .008), tumor differentiation (P < .001), vessel invasion (P = .001), plural invasion (P < .001), pT stage (P < .001), nodal involvement (P < .001), and pathological tumor node metastasis stage (P < .001). A cutoff point of SUVmax of 3.8 (P < .001) could be used to predict pathological nodal metastasis. Multivariable analyses indicated that preoperative SUVmax >3.8 (odds ratio, 12.149; P < .001) was an independent predictor of nodal metastasis. Overall survival analyses further suggested that SUVmax was an independent prognostic indicator (hazard ratio, 2.050; P = .017). CONCLUSION: Preoperative SUVmax is a predictor of pathological nodal metastasis and prognosis for peripheral cN0 NSCLC patients with tumor size ≤2 cm. Our results indicate that assessment of PET SUVmax could improve stratification of these patients.
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spelling pubmed-71318552020-04-06 Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer Wang, Shuai Lin, Dong Yang, Xiaodong Zhan, Cheng Zhao, Shihai Luo, Rongkui Wang, Qun Tan, Lijie Cancer Med Clinical Cancer Research OBJECTIVE: In this cohort study, we determined the clinical value of the maximum standardized uptake value (SUVmax) of primary tumors in non‐small cell lung cancer (NSCLC). STUDY DESIGN: A retrospective review of NSCLC patients was performed from January 2011 to December 2017. Peripheral cN0 NSCLC patients with tumor size ≤2 cm were included. SUVmax was calculated as a continuous variable for semiquantitative analyses. A receiver operating characteristic curve was analyzed to assess the cutoff threshold of SUVmax on pathological (p) nodal metastasis. We further evaluated the clinical relevance of SUVmax in peripheral cN0 NSCLC patients. RESULTS: A total of 670 peripheral NSCLC patients with tumor size ≤2 cm were deemed cN0 by preoperative PET/CT scan. Statistical analyses suggested significant correlations of SUVmax with smoking status (P = .026), tumor volume (P = .001), pathology type (P = .008), tumor differentiation (P < .001), vessel invasion (P = .001), plural invasion (P < .001), pT stage (P < .001), nodal involvement (P < .001), and pathological tumor node metastasis stage (P < .001). A cutoff point of SUVmax of 3.8 (P < .001) could be used to predict pathological nodal metastasis. Multivariable analyses indicated that preoperative SUVmax >3.8 (odds ratio, 12.149; P < .001) was an independent predictor of nodal metastasis. Overall survival analyses further suggested that SUVmax was an independent prognostic indicator (hazard ratio, 2.050; P = .017). CONCLUSION: Preoperative SUVmax is a predictor of pathological nodal metastasis and prognosis for peripheral cN0 NSCLC patients with tumor size ≤2 cm. Our results indicate that assessment of PET SUVmax could improve stratification of these patients. John Wiley and Sons Inc. 2020-02-13 /pmc/articles/PMC7131855/ /pubmed/32056387 http://dx.doi.org/10.1002/cam4.2900 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Wang, Shuai
Lin, Dong
Yang, Xiaodong
Zhan, Cheng
Zhao, Shihai
Luo, Rongkui
Wang, Qun
Tan, Lijie
Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title_full Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title_fullStr Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title_full_unstemmed Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title_short Clinical significance of PET/CT uptake for peripheral clinical N0 non‐small cell lung cancer
title_sort clinical significance of pet/ct uptake for peripheral clinical n0 non‐small cell lung cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131855/
https://www.ncbi.nlm.nih.gov/pubmed/32056387
http://dx.doi.org/10.1002/cam4.2900
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