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Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score

BACKGROUND: Poor prognosis associated with adenocarcinoma of International Association for the Study of Lung Cancer (IASLC) grade 3 has been recognized. In this study we aimed to develop a scoring system for predicting IASLC grade 3 based before surgery. METHODS: Two retrospective datasets with sign...

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Autores principales: Woo, Wongi, Cha, Yoon Jin, Park, Chul Hwan, Moon, Duk Hwan, Lee, Sungsoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317591/
https://www.ncbi.nlm.nih.gov/pubmed/37201906
http://dx.doi.org/10.1111/1759-7714.14932
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author Woo, Wongi
Cha, Yoon Jin
Park, Chul Hwan
Moon, Duk Hwan
Lee, Sungsoo
author_facet Woo, Wongi
Cha, Yoon Jin
Park, Chul Hwan
Moon, Duk Hwan
Lee, Sungsoo
author_sort Woo, Wongi
collection PubMed
description BACKGROUND: Poor prognosis associated with adenocarcinoma of International Association for the Study of Lung Cancer (IASLC) grade 3 has been recognized. In this study we aimed to develop a scoring system for predicting IASLC grade 3 based before surgery. METHODS: Two retrospective datasets with significant heterogeneity were used to develop and evaluate a scoring system. The development set was comprised of patients with pathological stage I nonmucinous adenocarcinoma and they were randomly divided into training (n = 375) and validation (n = 125) datasets. Using multivariate logistic regression, a scoring system was developed and internally validated. Later, this new score was further tested in the testing set which was comprised of patients with clinical stage 0–I non‐small cell lung cancer (NSCLC) (n = 281). RESULTS: Four factors that were related to IASLC grade 3 were used to develop the new scoring system the MOSS score; male (M, point 1), overweight (O, point 1), size>10 mm (S, point 1), and solid lesions (S, point 3). Predictability of IASLC grade 3 increased from 0.4% to 75.2% with scores from 0 to 6. The area under the curve (AUC) of the MOSS was 0.889 and 0.765 for the training and validation datasets, respectively. The MOSS score exhibited similar predictability in the testing set (AUC: 0.820). CONCLUSION: The MOSS score, which combines preoperative variables, can be used to identify high‐risk early‐stage NSCLC patients with aggressive histological features. It can support clinicians in determining a treatment plan and surgical extent. Further refinement of this scoring system with prospective validation is needed.
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spelling pubmed-103175912023-07-04 Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score Woo, Wongi Cha, Yoon Jin Park, Chul Hwan Moon, Duk Hwan Lee, Sungsoo Thorac Cancer Original Articles BACKGROUND: Poor prognosis associated with adenocarcinoma of International Association for the Study of Lung Cancer (IASLC) grade 3 has been recognized. In this study we aimed to develop a scoring system for predicting IASLC grade 3 based before surgery. METHODS: Two retrospective datasets with significant heterogeneity were used to develop and evaluate a scoring system. The development set was comprised of patients with pathological stage I nonmucinous adenocarcinoma and they were randomly divided into training (n = 375) and validation (n = 125) datasets. Using multivariate logistic regression, a scoring system was developed and internally validated. Later, this new score was further tested in the testing set which was comprised of patients with clinical stage 0–I non‐small cell lung cancer (NSCLC) (n = 281). RESULTS: Four factors that were related to IASLC grade 3 were used to develop the new scoring system the MOSS score; male (M, point 1), overweight (O, point 1), size>10 mm (S, point 1), and solid lesions (S, point 3). Predictability of IASLC grade 3 increased from 0.4% to 75.2% with scores from 0 to 6. The area under the curve (AUC) of the MOSS was 0.889 and 0.765 for the training and validation datasets, respectively. The MOSS score exhibited similar predictability in the testing set (AUC: 0.820). CONCLUSION: The MOSS score, which combines preoperative variables, can be used to identify high‐risk early‐stage NSCLC patients with aggressive histological features. It can support clinicians in determining a treatment plan and surgical extent. Further refinement of this scoring system with prospective validation is needed. John Wiley & Sons Australia, Ltd 2023-05-18 /pmc/articles/PMC10317591/ /pubmed/37201906 http://dx.doi.org/10.1111/1759-7714.14932 Text en © 2023 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. 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 Original Articles
Woo, Wongi
Cha, Yoon Jin
Park, Chul Hwan
Moon, Duk Hwan
Lee, Sungsoo
Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title_full Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title_fullStr Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title_full_unstemmed Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title_short Predictive scoring of high‐grade histology among early‐stage lung cancer patients: The MOSS score
title_sort predictive scoring of high‐grade histology among early‐stage lung cancer patients: the moss score
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317591/
https://www.ncbi.nlm.nih.gov/pubmed/37201906
http://dx.doi.org/10.1111/1759-7714.14932
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