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Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer
In this study, we investigated which N staging system was the most accurate at predicting survival in pancreatic cancer patients. Lymph node (LN) metastasis is known to be one of the important prognostic factors in resected pancreatic cancer. There are several LN evaluation systems to predict oncolo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937943/ https://www.ncbi.nlm.nih.gov/pubmed/27368029 http://dx.doi.org/10.1097/MD.0000000000004035 |
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author | Kim, Sung Hyun Hwang, Ho Kyoung Lee, Woo Jung Kang, Chang Moo |
author_facet | Kim, Sung Hyun Hwang, Ho Kyoung Lee, Woo Jung Kang, Chang Moo |
author_sort | Kim, Sung Hyun |
collection | PubMed |
description | In this study, we investigated which N staging system was the most accurate at predicting survival in pancreatic cancer patients. Lymph node (LN) metastasis is known to be one of the important prognostic factors in resected pancreatic cancer. There are several LN evaluation systems to predict oncologic impact. From January 1992 to December 2014, 77 medical records of patients who underwent radical pancreatectomy for left-sided pancreatic cancer were reviewed retrospectively. Clinicopathologic variables including pN stage, total number of retrieved LNs (N-RLN), lymph node ratio (LNR), and absolute number of LN metastases (N-LNmet) were evaluated. Disease-free survival (DFS) and disease-specific survival (DSS) were analyzed according to these 4 LN staging systems. In univariate analysis, pN stage (pN0 vs pN1: 17.5 months vs 7.9 months, P = 0.001), LNR (<0.08 vs ≥0.08: 17.5 months vs 4.4 months, P < 0.001), and N-LNmet (#N = 0 vs #N = 1 vs #N≥2: 17.5 months vs 11.0 months vs 6.4 months, P = 0.002) had a significant effect on DFS, whereas the pN stage (pN0 vs pN1: 35.3 months vs 16.7 months, P = 0.001), LNR (<0.08 vs ≥0.08: 37.1 months vs 15.0 months, P < 0.001), and N-LNmet (#N = 0 vs #N = 1 vs #N≥2: 35.3 months vs 18.4 months vs 16.4 months, P = 0.001) had a significant effect on DSS. In multivariate analysis, N-LNmet (#N≥2) was identified as an independent prognostic factor of oncologic outcome (DFS and DSS: Exp (β) = 2.83, P = 0.001, and Exp (β) = 3.17, P = 0.001, respectively). Absolute number of lymph node metastases predicted oncologic outcome in resected left-sided pancreatic cancer patients. |
format | Online Article Text |
id | pubmed-4937943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49379432016-08-18 Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer Kim, Sung Hyun Hwang, Ho Kyoung Lee, Woo Jung Kang, Chang Moo Medicine (Baltimore) 7100 In this study, we investigated which N staging system was the most accurate at predicting survival in pancreatic cancer patients. Lymph node (LN) metastasis is known to be one of the important prognostic factors in resected pancreatic cancer. There are several LN evaluation systems to predict oncologic impact. From January 1992 to December 2014, 77 medical records of patients who underwent radical pancreatectomy for left-sided pancreatic cancer were reviewed retrospectively. Clinicopathologic variables including pN stage, total number of retrieved LNs (N-RLN), lymph node ratio (LNR), and absolute number of LN metastases (N-LNmet) were evaluated. Disease-free survival (DFS) and disease-specific survival (DSS) were analyzed according to these 4 LN staging systems. In univariate analysis, pN stage (pN0 vs pN1: 17.5 months vs 7.9 months, P = 0.001), LNR (<0.08 vs ≥0.08: 17.5 months vs 4.4 months, P < 0.001), and N-LNmet (#N = 0 vs #N = 1 vs #N≥2: 17.5 months vs 11.0 months vs 6.4 months, P = 0.002) had a significant effect on DFS, whereas the pN stage (pN0 vs pN1: 35.3 months vs 16.7 months, P = 0.001), LNR (<0.08 vs ≥0.08: 37.1 months vs 15.0 months, P < 0.001), and N-LNmet (#N = 0 vs #N = 1 vs #N≥2: 35.3 months vs 18.4 months vs 16.4 months, P = 0.001) had a significant effect on DSS. In multivariate analysis, N-LNmet (#N≥2) was identified as an independent prognostic factor of oncologic outcome (DFS and DSS: Exp (β) = 2.83, P = 0.001, and Exp (β) = 3.17, P = 0.001, respectively). Absolute number of lymph node metastases predicted oncologic outcome in resected left-sided pancreatic cancer patients. Wolters Kluwer Health 2016-07-01 /pmc/articles/PMC4937943/ /pubmed/27368029 http://dx.doi.org/10.1097/MD.0000000000004035 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 7100 Kim, Sung Hyun Hwang, Ho Kyoung Lee, Woo Jung Kang, Chang Moo Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title | Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title_full | Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title_fullStr | Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title_full_unstemmed | Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title_short | Identification of an N staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
title_sort | identification of an n staging system that predicts oncologic outcome in resected left-sided pancreatic cancer |
topic | 7100 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937943/ https://www.ncbi.nlm.nih.gov/pubmed/27368029 http://dx.doi.org/10.1097/MD.0000000000004035 |
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