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The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma

BACKGROUND: Stage I pulmonary adenocarcinoma (PA) can offer an unfavorable prognosis. The aim of this study was to classify the prognosis of stage I PA on the basis of the lepidic component and to confirm whether the lepidic component can be used as a criterion for predicting the prognosis of stage...

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Autores principales: Moon, Youngkyu, Sung, Sook Whan, Lee, Kyo Young, Kim, Young Kyoon, Park, Jae Kil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754885/
https://www.ncbi.nlm.nih.gov/pubmed/26879575
http://dx.doi.org/10.1186/s12957-016-0791-y
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author Moon, Youngkyu
Sung, Sook Whan
Lee, Kyo Young
Kim, Young Kyoon
Park, Jae Kil
author_facet Moon, Youngkyu
Sung, Sook Whan
Lee, Kyo Young
Kim, Young Kyoon
Park, Jae Kil
author_sort Moon, Youngkyu
collection PubMed
description BACKGROUND: Stage I pulmonary adenocarcinoma (PA) can offer an unfavorable prognosis. The aim of this study was to classify the prognosis of stage I PA on the basis of the lepidic component and to confirm whether the lepidic component can be used as a criterion for predicting the prognosis of stage I PA. METHODS: We conducted a retrospective study of patients who underwent curative surgery for stage I and IIA PA. Stage I disease was divided into three groups on the basis of the lepidic component: group 1, ≤10 %; group 2, >10 to 50 %; and group 3, >50 %. We compared recurrence-free survival (RFS) rates among groups 1, 2, and 3, and stage IIA disease. We also evaluated risk factors for disease recurrence with multivariate analysis. RESULTS: A total of 224 patients were included in our study; most patients (n = 201) had stage I disease. Three-year RFS rates in group 1 (n = 73), group 2 (n = 75), and group 3 (n = 53) were 74.1, 90.4, and 90.0 %, respectively. There was a significant difference in RFS between group 1 and group 2 (p = 0.009). The 3-year RFS rate in stage IIA disease was 61.4 %. There were no significant differences in RFS between group 1 and stage IIA disease (p = 0.163). In multivariate analysis, group 1 had the highest risk of recurrence (HR 5.806, p = 0.006) in stage I PA. CONCLUSIONS: Stage I PA with a lepidic component ≤10 % was associated with an unfavorable prognosis that was similar to the prognosis of stage IIA disease. The prognosis for stage I PA should not be based on general criteria, but instead, the lepidic component should be evaluated and considered when determining disease prognosis.
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spelling pubmed-47548852016-02-17 The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma Moon, Youngkyu Sung, Sook Whan Lee, Kyo Young Kim, Young Kyoon Park, Jae Kil World J Surg Oncol Research BACKGROUND: Stage I pulmonary adenocarcinoma (PA) can offer an unfavorable prognosis. The aim of this study was to classify the prognosis of stage I PA on the basis of the lepidic component and to confirm whether the lepidic component can be used as a criterion for predicting the prognosis of stage I PA. METHODS: We conducted a retrospective study of patients who underwent curative surgery for stage I and IIA PA. Stage I disease was divided into three groups on the basis of the lepidic component: group 1, ≤10 %; group 2, >10 to 50 %; and group 3, >50 %. We compared recurrence-free survival (RFS) rates among groups 1, 2, and 3, and stage IIA disease. We also evaluated risk factors for disease recurrence with multivariate analysis. RESULTS: A total of 224 patients were included in our study; most patients (n = 201) had stage I disease. Three-year RFS rates in group 1 (n = 73), group 2 (n = 75), and group 3 (n = 53) were 74.1, 90.4, and 90.0 %, respectively. There was a significant difference in RFS between group 1 and group 2 (p = 0.009). The 3-year RFS rate in stage IIA disease was 61.4 %. There were no significant differences in RFS between group 1 and stage IIA disease (p = 0.163). In multivariate analysis, group 1 had the highest risk of recurrence (HR 5.806, p = 0.006) in stage I PA. CONCLUSIONS: Stage I PA with a lepidic component ≤10 % was associated with an unfavorable prognosis that was similar to the prognosis of stage IIA disease. The prognosis for stage I PA should not be based on general criteria, but instead, the lepidic component should be evaluated and considered when determining disease prognosis. BioMed Central 2016-02-16 /pmc/articles/PMC4754885/ /pubmed/26879575 http://dx.doi.org/10.1186/s12957-016-0791-y Text en © Moon et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Moon, Youngkyu
Sung, Sook Whan
Lee, Kyo Young
Kim, Young Kyoon
Park, Jae Kil
The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title_full The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title_fullStr The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title_full_unstemmed The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title_short The importance of the lepidic component as a prognostic factor in stage I pulmonary adenocarcinoma
title_sort importance of the lepidic component as a prognostic factor in stage i pulmonary adenocarcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754885/
https://www.ncbi.nlm.nih.gov/pubmed/26879575
http://dx.doi.org/10.1186/s12957-016-0791-y
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