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The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung
BACKGROUND: The literature is inconclusive as to whether the percentage of the lepidic component of an invasive adenocarcinoma (AC) of the lung influences prognosis. We studied a population-based series of selected, resected invasive pulmonary ACs to determine if incremental increases in the lepidic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498518/ https://www.ncbi.nlm.nih.gov/pubmed/26159539 http://dx.doi.org/10.1186/s13000-015-0335-8 |
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author | Strand, Trond-Eirik Rostad, Hans Strøm, Erik H. Hasleton, Philip |
author_facet | Strand, Trond-Eirik Rostad, Hans Strøm, Erik H. Hasleton, Philip |
author_sort | Strand, Trond-Eirik |
collection | PubMed |
description | BACKGROUND: The literature is inconclusive as to whether the percentage of the lepidic component of an invasive adenocarcinoma (AC) of the lung influences prognosis. We studied a population-based series of selected, resected invasive pulmonary ACs to determine if incremental increases in the lepidic component were an independent, prognostic variable. METHODS: Patients undergoing resection for lung cancer reported to the Cancer Registry of Norway and diagnosed in the period 1993-2002 with a bronchioloalveolar carcinoma (BAC) (old terminology) (adenocarcinoma in situ, AIS in the new terminology) in the lung were selected. A pulmonary pathologist reviewed all sections and estimated the percentage of the lepidic component. Follow-up of survival was to the end of 2013. RESULTS: One hundred thirty-one patients were identified, 102 had AC with lepidic growth. Of these, 44 had AC with a component of lepidic growth less than 50 % and seven had AC with 95 % lepidic component or more. One of the latter cases was considered to be AIS. In regression analyses, superior survival was associated with a greater lepidic component (p = 0.041). Mucinous tumors had a worse prognosis than non-mucinous (p = 0.012) in regression analyses, as did increasing age and stage. The five-year observed survival was 69.0 % for non-mucinous cases and 66.7 % for the group with a lepidic component of 80 % or greater. CONCLUSION: The percentage of the lepidic component appears to be an independent, significant prognostic factor in a selection of pulmonary AC. |
format | Online Article Text |
id | pubmed-4498518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44985182015-07-11 The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung Strand, Trond-Eirik Rostad, Hans Strøm, Erik H. Hasleton, Philip Diagn Pathol Research BACKGROUND: The literature is inconclusive as to whether the percentage of the lepidic component of an invasive adenocarcinoma (AC) of the lung influences prognosis. We studied a population-based series of selected, resected invasive pulmonary ACs to determine if incremental increases in the lepidic component were an independent, prognostic variable. METHODS: Patients undergoing resection for lung cancer reported to the Cancer Registry of Norway and diagnosed in the period 1993-2002 with a bronchioloalveolar carcinoma (BAC) (old terminology) (adenocarcinoma in situ, AIS in the new terminology) in the lung were selected. A pulmonary pathologist reviewed all sections and estimated the percentage of the lepidic component. Follow-up of survival was to the end of 2013. RESULTS: One hundred thirty-one patients were identified, 102 had AC with lepidic growth. Of these, 44 had AC with a component of lepidic growth less than 50 % and seven had AC with 95 % lepidic component or more. One of the latter cases was considered to be AIS. In regression analyses, superior survival was associated with a greater lepidic component (p = 0.041). Mucinous tumors had a worse prognosis than non-mucinous (p = 0.012) in regression analyses, as did increasing age and stage. The five-year observed survival was 69.0 % for non-mucinous cases and 66.7 % for the group with a lepidic component of 80 % or greater. CONCLUSION: The percentage of the lepidic component appears to be an independent, significant prognostic factor in a selection of pulmonary AC. BioMed Central 2015-07-09 /pmc/articles/PMC4498518/ /pubmed/26159539 http://dx.doi.org/10.1186/s13000-015-0335-8 Text en © Strand et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Strand, Trond-Eirik Rostad, Hans Strøm, Erik H. Hasleton, Philip The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title | The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title_full | The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title_fullStr | The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title_full_unstemmed | The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title_short | The percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
title_sort | percentage of lepidic growth is an independent prognostic factor in invasive adenocarcinoma of the lung |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498518/ https://www.ncbi.nlm.nih.gov/pubmed/26159539 http://dx.doi.org/10.1186/s13000-015-0335-8 |
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