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Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer

BACKGROUND: Patients with pathologic stage (p-Stage) IA non-small cell lung cancer (NSCLC) have a good survival rate because of possible curative resection. However, up to 10% of these patients relapse postoperatively. To identify unfavorable prognostic factors, we retrospectively analyzed the clini...

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Autores principales: Hamanaka, Rurika, Yokose, Tomoyuki, Sakuma, Yuji, Tsuboi, Masahiro, Ito, Hiroyuki, Nakayama, Haruhiko, Yamada, Kouzo, Masuda, Ryota, Iwazaki, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413537/
https://www.ncbi.nlm.nih.gov/pubmed/25884820
http://dx.doi.org/10.1186/s13000-015-0249-5
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author Hamanaka, Rurika
Yokose, Tomoyuki
Sakuma, Yuji
Tsuboi, Masahiro
Ito, Hiroyuki
Nakayama, Haruhiko
Yamada, Kouzo
Masuda, Ryota
Iwazaki, Masayuki
author_facet Hamanaka, Rurika
Yokose, Tomoyuki
Sakuma, Yuji
Tsuboi, Masahiro
Ito, Hiroyuki
Nakayama, Haruhiko
Yamada, Kouzo
Masuda, Ryota
Iwazaki, Masayuki
author_sort Hamanaka, Rurika
collection PubMed
description BACKGROUND: Patients with pathologic stage (p-Stage) IA non-small cell lung cancer (NSCLC) have a good survival rate because of possible curative resection. However, up to 10% of these patients relapse postoperatively. To identify unfavorable prognostic factors, we retrospectively analyzed the clinicopathological features of p-Stage IA disease, focusing on vascular invasion. METHODS: Of 467 patients with p-Stage I NSCLC, 335 were diagnosed with p-Stage IA or IB disease based on a lesion size ≤3 cm and the presence of pleural invasion (PL). Univariate and multivariate analyses of recurrence-free survival (RFS) were performed with age, sex, PL, and vascular invasion (blood vessel invasion [v] and lymphatic vessel invasion [ly]) as variables. To examine vascular invasion, hematoxylin-eosin (HE), Elastica van Gieson staining, and immunostaining with anti-podoplanin antibody were performed. The presence or absence of v and ly was recorded; the number of involved vessels was counted. Survival rates were obtained using the Kaplan–Meier method and log-rank test. Multivariate analyses were performed using the Cox proportional hazards model. RESULTS: RFS differed significantly between patients with no or one involved blood vessel (0 v or 1 v) and those with ≥2 involved vessels (≥2 v). Similarly, RFS differed significantly between patients with no lymphatic vessel involvement (0 ly) and those with one involved lymphatic vessel (1 ly). Thus, BVI(+) and BVI(−) were defined as ≥2 v and 0 v + 1 v, and LVI(+) and LVI(−) as ≥1 ly and 0 ly, respectively. BVI and LVI together represented tumor vessel invasion (TVI). On multivariate analyses, PL and TVI were independently associated with recurrence. Additionally, patients with p-Stage IA TVI(+) disease had a comparable recurrence rate to those with p-Stage IB disease. CONCLUSIONS: Similar to PL, TVI is an important factor increasing the likelihood of recurrence. As HE staining alone is insufficient for evaluating vascular invasion, specific staining is necessary. Moreover, patients with p-Stage IA TVI(+) disease had a recurrence rate comparable to those with p-Stage IB disease; therefore, further studies should aim to elucidate whether patients with p-Stage IA TVI(+) disease should be administered postoperative chemotherapy similar to that received by p-Stage IB patients. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5213064891369688
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spelling pubmed-44135372015-04-30 Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer Hamanaka, Rurika Yokose, Tomoyuki Sakuma, Yuji Tsuboi, Masahiro Ito, Hiroyuki Nakayama, Haruhiko Yamada, Kouzo Masuda, Ryota Iwazaki, Masayuki Diagn Pathol Research BACKGROUND: Patients with pathologic stage (p-Stage) IA non-small cell lung cancer (NSCLC) have a good survival rate because of possible curative resection. However, up to 10% of these patients relapse postoperatively. To identify unfavorable prognostic factors, we retrospectively analyzed the clinicopathological features of p-Stage IA disease, focusing on vascular invasion. METHODS: Of 467 patients with p-Stage I NSCLC, 335 were diagnosed with p-Stage IA or IB disease based on a lesion size ≤3 cm and the presence of pleural invasion (PL). Univariate and multivariate analyses of recurrence-free survival (RFS) were performed with age, sex, PL, and vascular invasion (blood vessel invasion [v] and lymphatic vessel invasion [ly]) as variables. To examine vascular invasion, hematoxylin-eosin (HE), Elastica van Gieson staining, and immunostaining with anti-podoplanin antibody were performed. The presence or absence of v and ly was recorded; the number of involved vessels was counted. Survival rates were obtained using the Kaplan–Meier method and log-rank test. Multivariate analyses were performed using the Cox proportional hazards model. RESULTS: RFS differed significantly between patients with no or one involved blood vessel (0 v or 1 v) and those with ≥2 involved vessels (≥2 v). Similarly, RFS differed significantly between patients with no lymphatic vessel involvement (0 ly) and those with one involved lymphatic vessel (1 ly). Thus, BVI(+) and BVI(−) were defined as ≥2 v and 0 v + 1 v, and LVI(+) and LVI(−) as ≥1 ly and 0 ly, respectively. BVI and LVI together represented tumor vessel invasion (TVI). On multivariate analyses, PL and TVI were independently associated with recurrence. Additionally, patients with p-Stage IA TVI(+) disease had a comparable recurrence rate to those with p-Stage IB disease. CONCLUSIONS: Similar to PL, TVI is an important factor increasing the likelihood of recurrence. As HE staining alone is insufficient for evaluating vascular invasion, specific staining is necessary. Moreover, patients with p-Stage IA TVI(+) disease had a recurrence rate comparable to those with p-Stage IB disease; therefore, further studies should aim to elucidate whether patients with p-Stage IA TVI(+) disease should be administered postoperative chemotherapy similar to that received by p-Stage IB patients. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5213064891369688 BioMed Central 2015-04-02 /pmc/articles/PMC4413537/ /pubmed/25884820 http://dx.doi.org/10.1186/s13000-015-0249-5 Text en © Hamanaka et al.; licensee BioMed Central. 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
Hamanaka, Rurika
Yokose, Tomoyuki
Sakuma, Yuji
Tsuboi, Masahiro
Ito, Hiroyuki
Nakayama, Haruhiko
Yamada, Kouzo
Masuda, Ryota
Iwazaki, Masayuki
Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title_full Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title_fullStr Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title_full_unstemmed Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title_short Prognostic impact of vascular invasion and standardization of its evaluation in stage I non-small cell lung cancer
title_sort prognostic impact of vascular invasion and standardization of its evaluation in stage i non-small cell lung cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413537/
https://www.ncbi.nlm.nih.gov/pubmed/25884820
http://dx.doi.org/10.1186/s13000-015-0249-5
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