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Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors

BACKGROUND: Thymic epithelial tumors (TETs) exhibit irregular shapes reflective of the heterogeneity in tumor growth and invasive properties. We aimed to identify the prognostic value of the pathological tumor long‐to‐short axis (L/S) ratio in TETs. METHODS: A retrospective study was performed on pa...

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Autores principales: Tian, Dong, Shiiya, Haruhiko, Sato, Masaaki, Shinozaki‐Ushiku, Aya, Yan, Hao‐Ji, Nakajima, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436687/
https://www.ncbi.nlm.nih.gov/pubmed/35861051
http://dx.doi.org/10.1111/1759-7714.14582
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author Tian, Dong
Shiiya, Haruhiko
Sato, Masaaki
Shinozaki‐Ushiku, Aya
Yan, Hao‐Ji
Nakajima, Jun
author_facet Tian, Dong
Shiiya, Haruhiko
Sato, Masaaki
Shinozaki‐Ushiku, Aya
Yan, Hao‐Ji
Nakajima, Jun
author_sort Tian, Dong
collection PubMed
description BACKGROUND: Thymic epithelial tumors (TETs) exhibit irregular shapes reflective of the heterogeneity in tumor growth and invasive properties. We aimed to identify the prognostic value of the pathological tumor long‐to‐short axis (L/S) ratio in TETs. METHODS: A retrospective study was performed on patients with TETs who underwent extended thymectomy between January 1999 and December 2019 in our institute. Patients were divided into two groups according to the threshold of the L/S ratio. Overall survival (OS) and progression‐free survival (PFS) were evaluated by Kaplan‐Meier analysis. The independent prognostic factors of TETs were identified by multivariate analysis. The performance of prediction models for the above survival outcomes with and without the L/S ratio was evaluated using an integrated time‐dependent area under the curve (iAUC). RESULTS: Eligible patients were divided into two groups based on higher (n = 42) and lower (n = 94) L/S ratios according to a threshold value of 1.39. A significant difference was found between the two groups only in disease progression (p = 0.001). Poorer survival outcomes were found from Kaplan‐Meier curves in the higher L/S ratio group (p < 0.05). In the multivariable analysis, the L/S ratio showed significant effects on OS and PFS (p < 0.05). The performance of models with the L/S ratio was better than that without the L/S ratio in predicting survival outcomes. CONCLUSIONS: The pathological tumor L/S ratio is an independent prognostic factor for OS and PFS in patients with TETs, and an L/S ratio >1.39 is associated with worse survival outcomes.
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spelling pubmed-94366872022-09-09 Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors Tian, Dong Shiiya, Haruhiko Sato, Masaaki Shinozaki‐Ushiku, Aya Yan, Hao‐Ji Nakajima, Jun Thorac Cancer Original Articles BACKGROUND: Thymic epithelial tumors (TETs) exhibit irregular shapes reflective of the heterogeneity in tumor growth and invasive properties. We aimed to identify the prognostic value of the pathological tumor long‐to‐short axis (L/S) ratio in TETs. METHODS: A retrospective study was performed on patients with TETs who underwent extended thymectomy between January 1999 and December 2019 in our institute. Patients were divided into two groups according to the threshold of the L/S ratio. Overall survival (OS) and progression‐free survival (PFS) were evaluated by Kaplan‐Meier analysis. The independent prognostic factors of TETs were identified by multivariate analysis. The performance of prediction models for the above survival outcomes with and without the L/S ratio was evaluated using an integrated time‐dependent area under the curve (iAUC). RESULTS: Eligible patients were divided into two groups based on higher (n = 42) and lower (n = 94) L/S ratios according to a threshold value of 1.39. A significant difference was found between the two groups only in disease progression (p = 0.001). Poorer survival outcomes were found from Kaplan‐Meier curves in the higher L/S ratio group (p < 0.05). In the multivariable analysis, the L/S ratio showed significant effects on OS and PFS (p < 0.05). The performance of models with the L/S ratio was better than that without the L/S ratio in predicting survival outcomes. CONCLUSIONS: The pathological tumor L/S ratio is an independent prognostic factor for OS and PFS in patients with TETs, and an L/S ratio >1.39 is associated with worse survival outcomes. John Wiley & Sons Australia, Ltd 2022-07-21 2022-09 /pmc/articles/PMC9436687/ /pubmed/35861051 http://dx.doi.org/10.1111/1759-7714.14582 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tian, Dong
Shiiya, Haruhiko
Sato, Masaaki
Shinozaki‐Ushiku, Aya
Yan, Hao‐Ji
Nakajima, Jun
Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title_full Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title_fullStr Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title_full_unstemmed Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title_short Pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
title_sort pathological tumor long‐to‐short axis ratio as a prognostic factor in patients with thymic epithelial tumors
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436687/
https://www.ncbi.nlm.nih.gov/pubmed/35861051
http://dx.doi.org/10.1111/1759-7714.14582
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