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Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma
OBJECTIVE: Invasive lung adenocarcinoma is composed of five different histological subgroups with diverse biological behavior and heterogeneous morphology, the acinar/papillary-predominant lung adenocarcinomas are the most common subgroups and recognized as an intermediate-grade group. In the real w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816566/ https://www.ncbi.nlm.nih.gov/pubmed/36620572 http://dx.doi.org/10.3389/fonc.2022.1090544 |
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author | Liu, Wei Zhang, Qian Zhang, Tiantian Li, Li Xu, Chunhua |
author_facet | Liu, Wei Zhang, Qian Zhang, Tiantian Li, Li Xu, Chunhua |
author_sort | Liu, Wei |
collection | PubMed |
description | OBJECTIVE: Invasive lung adenocarcinoma is composed of five different histological subgroups with diverse biological behavior and heterogeneous morphology, the acinar/papillary-predominant lung adenocarcinomas are the most common subgroups and recognized as an intermediate-grade group. In the real world, clinicians primarily consider predominant patterns and ignore the impact of minor components in the prognosis of lung adenocarcinoma. The study evaluated the clinicopathologic characteristics of the lepidic, solid, and micropapillary patterns as non-predominant components and whether the minimal patterns had prognostic value on acinar/papillary-predominant lung adenocarcinomas. METHODS: A total of 153 acinar/papillary-predominant lung adenocarcinoma patients with tumor size ≤4 cm were classified into four risk subgroups based on the presence of lepidic and micropapillary/solid components: MP/S(−)Lep(+), MP/S(+)Lep(+), MP/S(−)Lep(−), and MP/S(+)Lep(−) groups. The Cox-proportional hazard regression model was used to assess disease-free survival (DFS). RESULTS: The risk subgroups based on the non-predominant patterns were associated with differentiation (P = 0.001), lymphovascular invasion (P = 0.001), and recurrence (P = 0.003). In univariate analysis, DFS was correlated with non-predominant components (P = 0.014), lymphovascular invasion (P = 0.001), carcinoembryonic antigen (CEA) (P = 0.001), and platelet-to-lymphocyte ratio (PLR) (P = 0.012). In the multivariate analysis, non-predominant components (P = 0.043) and PLR (P = 0.032) were independent prognostic factors for DFS. The 5-year survival rates of MP/S(−)Lep(+), MP/S(+)Lep(+), MP/S(−)Lep(−) and MP/S(+)Lep(−) subgroups were 93.1%,92.9%,73.1%,61.9%, respectively. The MP/S(−)Lep(+) subgroup had the favorable prognosis than MP/S(+)Lep(−) subgroup with a statistically significant difference (P = 0.002). As minor components, the lepidic patterns were a protective factor, and the solid and micropapillary components were poor factors. The recurrence was related to the presence of non-predominant patterns rather than their proportion. Adjuvant chemotherapy did not significantly improve the prognosis of the MP/S(+)Lep(-) subgroup (P = 0.839). CONCLUSIONS: Regardless of the proportion, the presence of micropapillary/solid components and the absence of lepidic patterns are aggressive factors of DFS in patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-9816566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98165662023-01-07 Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma Liu, Wei Zhang, Qian Zhang, Tiantian Li, Li Xu, Chunhua Front Oncol Oncology OBJECTIVE: Invasive lung adenocarcinoma is composed of five different histological subgroups with diverse biological behavior and heterogeneous morphology, the acinar/papillary-predominant lung adenocarcinomas are the most common subgroups and recognized as an intermediate-grade group. In the real world, clinicians primarily consider predominant patterns and ignore the impact of minor components in the prognosis of lung adenocarcinoma. The study evaluated the clinicopathologic characteristics of the lepidic, solid, and micropapillary patterns as non-predominant components and whether the minimal patterns had prognostic value on acinar/papillary-predominant lung adenocarcinomas. METHODS: A total of 153 acinar/papillary-predominant lung adenocarcinoma patients with tumor size ≤4 cm were classified into four risk subgroups based on the presence of lepidic and micropapillary/solid components: MP/S(−)Lep(+), MP/S(+)Lep(+), MP/S(−)Lep(−), and MP/S(+)Lep(−) groups. The Cox-proportional hazard regression model was used to assess disease-free survival (DFS). RESULTS: The risk subgroups based on the non-predominant patterns were associated with differentiation (P = 0.001), lymphovascular invasion (P = 0.001), and recurrence (P = 0.003). In univariate analysis, DFS was correlated with non-predominant components (P = 0.014), lymphovascular invasion (P = 0.001), carcinoembryonic antigen (CEA) (P = 0.001), and platelet-to-lymphocyte ratio (PLR) (P = 0.012). In the multivariate analysis, non-predominant components (P = 0.043) and PLR (P = 0.032) were independent prognostic factors for DFS. The 5-year survival rates of MP/S(−)Lep(+), MP/S(+)Lep(+), MP/S(−)Lep(−) and MP/S(+)Lep(−) subgroups were 93.1%,92.9%,73.1%,61.9%, respectively. The MP/S(−)Lep(+) subgroup had the favorable prognosis than MP/S(+)Lep(−) subgroup with a statistically significant difference (P = 0.002). As minor components, the lepidic patterns were a protective factor, and the solid and micropapillary components were poor factors. The recurrence was related to the presence of non-predominant patterns rather than their proportion. Adjuvant chemotherapy did not significantly improve the prognosis of the MP/S(+)Lep(-) subgroup (P = 0.839). CONCLUSIONS: Regardless of the proportion, the presence of micropapillary/solid components and the absence of lepidic patterns are aggressive factors of DFS in patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816566/ /pubmed/36620572 http://dx.doi.org/10.3389/fonc.2022.1090544 Text en Copyright © 2022 Liu, Zhang, Zhang, Li and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Liu, Wei Zhang, Qian Zhang, Tiantian Li, Li Xu, Chunhua Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title | Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title_full | Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title_fullStr | Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title_full_unstemmed | Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title_short | Minor histological components predict the recurrence of patients with resected stage I acinar- or papillary-predominant lung adenocarcinoma |
title_sort | minor histological components predict the recurrence of patients with resected stage i acinar- or papillary-predominant lung adenocarcinoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816566/ https://www.ncbi.nlm.nih.gov/pubmed/36620572 http://dx.doi.org/10.3389/fonc.2022.1090544 |
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