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A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer
Purpose: To develop an effective diagnostic model for bone metastasis of gastric cancer by combining (18)F-FDG PET/CT and clinical data. Materials and Methods: A total of 212 gastric cancer patients with abnormal bone imaging scans based on (18)F-FDG PET/CT were retrospectively enrolled between Sept...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712756/ https://www.ncbi.nlm.nih.gov/pubmed/34970546 http://dx.doi.org/10.3389/fcell.2021.783466 |
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author | Wu, Chunhui Lin, Xiaoping Li, Zhoulei Chen, Zhifeng Xie, Wenhui Zhang, Xiangsong Wang, Xiaoyan |
author_facet | Wu, Chunhui Lin, Xiaoping Li, Zhoulei Chen, Zhifeng Xie, Wenhui Zhang, Xiangsong Wang, Xiaoyan |
author_sort | Wu, Chunhui |
collection | PubMed |
description | Purpose: To develop an effective diagnostic model for bone metastasis of gastric cancer by combining (18)F-FDG PET/CT and clinical data. Materials and Methods: A total of 212 gastric cancer patients with abnormal bone imaging scans based on (18)F-FDG PET/CT were retrospectively enrolled between September 2009 and March 2020. Risk factors for bone metastasis of gastric cancer were identified by multivariate logistic regression analysis and used to create a nomogram. The performance of the nomogram was evaluated by using receiver operating characteristic curves and calibration plots. Results: The diagnostic power of the binary logistic regression model incorporating skeleton-related symptoms, anemia, the SUVmax of bone lesions, bone changes, the location of bone lesions, ALP, LDH, CEA, and CA19-9 was significantly higher than that of the model using only clinical factors (p = 0.008). The diagnostic model for bone metastasis of gastric cancer using a combination of clinical and imaging data showed an appropriate goodness of fit according to a calibration test (p = 0.294) and good discriminating ability (AUC = 0.925). Conclusions: The diagnostic model combined with the (18)F-FDG PET/CT findings and clinical data showed a better diagnosis performance for bone metastasis of gastric cancer than the other studied models. Compared with the model using clinical factors alone, the additional (18)F-FDG PET/CT findings could improve the diagnostic efficacy of identifying bone metastases in gastric cancer. |
format | Online Article Text |
id | pubmed-8712756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87127562021-12-29 A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer Wu, Chunhui Lin, Xiaoping Li, Zhoulei Chen, Zhifeng Xie, Wenhui Zhang, Xiangsong Wang, Xiaoyan Front Cell Dev Biol Cell and Developmental Biology Purpose: To develop an effective diagnostic model for bone metastasis of gastric cancer by combining (18)F-FDG PET/CT and clinical data. Materials and Methods: A total of 212 gastric cancer patients with abnormal bone imaging scans based on (18)F-FDG PET/CT were retrospectively enrolled between September 2009 and March 2020. Risk factors for bone metastasis of gastric cancer were identified by multivariate logistic regression analysis and used to create a nomogram. The performance of the nomogram was evaluated by using receiver operating characteristic curves and calibration plots. Results: The diagnostic power of the binary logistic regression model incorporating skeleton-related symptoms, anemia, the SUVmax of bone lesions, bone changes, the location of bone lesions, ALP, LDH, CEA, and CA19-9 was significantly higher than that of the model using only clinical factors (p = 0.008). The diagnostic model for bone metastasis of gastric cancer using a combination of clinical and imaging data showed an appropriate goodness of fit according to a calibration test (p = 0.294) and good discriminating ability (AUC = 0.925). Conclusions: The diagnostic model combined with the (18)F-FDG PET/CT findings and clinical data showed a better diagnosis performance for bone metastasis of gastric cancer than the other studied models. Compared with the model using clinical factors alone, the additional (18)F-FDG PET/CT findings could improve the diagnostic efficacy of identifying bone metastases in gastric cancer. Frontiers Media S.A. 2021-12-14 /pmc/articles/PMC8712756/ /pubmed/34970546 http://dx.doi.org/10.3389/fcell.2021.783466 Text en Copyright © 2021 Wu, Lin, Li, Chen, Xie, Zhang and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Wu, Chunhui Lin, Xiaoping Li, Zhoulei Chen, Zhifeng Xie, Wenhui Zhang, Xiangsong Wang, Xiaoyan A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title | A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title_full | A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title_fullStr | A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title_full_unstemmed | A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title_short | A Diagnostic Nomogram Based on (18)F-FDG PET/CT for Bone Metastasis of Gastric Cancer |
title_sort | diagnostic nomogram based on (18)f-fdg pet/ct for bone metastasis of gastric cancer |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712756/ https://www.ncbi.nlm.nih.gov/pubmed/34970546 http://dx.doi.org/10.3389/fcell.2021.783466 |
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