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Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies
OBJECTIVES: This study aimed to evaluate the diagnostic performance of the lung zero-echo time (ZTE) sequence in FDG PET/MRI for detection and differentiation of lung lesions in oncologic patients in comparison with conventional two-point Dixon-based MR imaging. METHODS: In this single-institution r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431435/ https://www.ncbi.nlm.nih.gov/pubmed/32300969 http://dx.doi.org/10.1007/s00330-020-06848-z |
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author | Zeng, Feibi Nogami, Munenobu Ueno, Yoshiko R. Kanda, Tomonori Sofue, Keitaro Kubo, Kazuhiro Kurimoto, Takako Murakami, Takamichi |
author_facet | Zeng, Feibi Nogami, Munenobu Ueno, Yoshiko R. Kanda, Tomonori Sofue, Keitaro Kubo, Kazuhiro Kurimoto, Takako Murakami, Takamichi |
author_sort | Zeng, Feibi |
collection | PubMed |
description | OBJECTIVES: This study aimed to evaluate the diagnostic performance of the lung zero-echo time (ZTE) sequence in FDG PET/MRI for detection and differentiation of lung lesions in oncologic patients in comparison with conventional two-point Dixon-based MR imaging. METHODS: In this single-institution retrospective study approved by the institutional review board, 209 patients with malignancies (97 men and 112 women; age range, 17–89 years; mean age, 66.5 ± 12.9 years) underwent (18)F-FDG PET/MRI between August 2017 and August 2018, with diagnostic Dixon and ZTE under respiratory gating acquired simultaneously with PET. Image analysis was performed for PET/Dixon and PET/ZTE fused images by two readers to assess the detectability and differentiation of lung lesions. The reference standard was pathological findings and/or the data from a chest CT. The detection and differentiation abilities were evaluated for all lesions and subgroups divided by lesion size and maximum standardized uptake value (SUVmax). RESULTS: Based on the reference standard, 227 lung lesions were identified in 113 patients. The detectability of PET/ZTE was significantly better than that of PET/Dixon for overall lesions, lesions with a SUVmax less than 3.0 and lesions smaller than 4 mm (p < 0.01). The diagnostic performance of PET/ZTE was significantly better than that of PET/Dixon for overall lesions and lesions smaller than 4 mm (p < 0.01). CONCLUSIONS: ZTE can improve diagnostic performance in the detection and differentiation of both FDG-avid and non-FDG-avid lung lesions smaller than 4 mm in size, yielding a promising tool to enhance the utility of FDG PET/MRI in oncology patients with lung lesions. KEY POINTS: • The detection rate of PET/ZTE for lesions with a SUVmax of less than 1.0 was significantly better than that of PET/Dixon. • The performance for differentiation of PET/ZTE for lesions that were even smaller than 4 mm in size were significantly better than that of PET/Dixon. • Inter-rater agreement of PET/ZTE for the differentiation of lesions less than 4 mm in size was substantial and better than that of PET/Dixon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-06848-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7431435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-74314352020-08-19 Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies Zeng, Feibi Nogami, Munenobu Ueno, Yoshiko R. Kanda, Tomonori Sofue, Keitaro Kubo, Kazuhiro Kurimoto, Takako Murakami, Takamichi Eur Radiol Oncology OBJECTIVES: This study aimed to evaluate the diagnostic performance of the lung zero-echo time (ZTE) sequence in FDG PET/MRI for detection and differentiation of lung lesions in oncologic patients in comparison with conventional two-point Dixon-based MR imaging. METHODS: In this single-institution retrospective study approved by the institutional review board, 209 patients with malignancies (97 men and 112 women; age range, 17–89 years; mean age, 66.5 ± 12.9 years) underwent (18)F-FDG PET/MRI between August 2017 and August 2018, with diagnostic Dixon and ZTE under respiratory gating acquired simultaneously with PET. Image analysis was performed for PET/Dixon and PET/ZTE fused images by two readers to assess the detectability and differentiation of lung lesions. The reference standard was pathological findings and/or the data from a chest CT. The detection and differentiation abilities were evaluated for all lesions and subgroups divided by lesion size and maximum standardized uptake value (SUVmax). RESULTS: Based on the reference standard, 227 lung lesions were identified in 113 patients. The detectability of PET/ZTE was significantly better than that of PET/Dixon for overall lesions, lesions with a SUVmax less than 3.0 and lesions smaller than 4 mm (p < 0.01). The diagnostic performance of PET/ZTE was significantly better than that of PET/Dixon for overall lesions and lesions smaller than 4 mm (p < 0.01). CONCLUSIONS: ZTE can improve diagnostic performance in the detection and differentiation of both FDG-avid and non-FDG-avid lung lesions smaller than 4 mm in size, yielding a promising tool to enhance the utility of FDG PET/MRI in oncology patients with lung lesions. KEY POINTS: • The detection rate of PET/ZTE for lesions with a SUVmax of less than 1.0 was significantly better than that of PET/Dixon. • The performance for differentiation of PET/ZTE for lesions that were even smaller than 4 mm in size were significantly better than that of PET/Dixon. • Inter-rater agreement of PET/ZTE for the differentiation of lesions less than 4 mm in size was substantial and better than that of PET/Dixon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-06848-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-04-16 2020 /pmc/articles/PMC7431435/ /pubmed/32300969 http://dx.doi.org/10.1007/s00330-020-06848-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Oncology Zeng, Feibi Nogami, Munenobu Ueno, Yoshiko R. Kanda, Tomonori Sofue, Keitaro Kubo, Kazuhiro Kurimoto, Takako Murakami, Takamichi Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title | Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title_full | Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title_fullStr | Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title_full_unstemmed | Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title_short | Diagnostic performance of zero-TE lung MR imaging in FDG PET/MRI for pulmonary malignancies |
title_sort | diagnostic performance of zero-te lung mr imaging in fdg pet/mri for pulmonary malignancies |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431435/ https://www.ncbi.nlm.nih.gov/pubmed/32300969 http://dx.doi.org/10.1007/s00330-020-06848-z |
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