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Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location
We aimed to identify clinicopathological differences and factors affecting survival outcomes of stage T2a and T2b gallbladder cancer (GBC) and validate the oncological benefits of regional lymphadenectomy and hepatic resection in these patients. This single-center study enrolled patients who were di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133080/ https://www.ncbi.nlm.nih.gov/pubmed/32233806 http://dx.doi.org/10.1177/1073274820915514 |
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author | Kim, Wan-Joon Lim, Tae-Wan Park, Pyoung-Jae Choi, Sae-Byeol Kim, Wan-Bae |
author_facet | Kim, Wan-Joon Lim, Tae-Wan Park, Pyoung-Jae Choi, Sae-Byeol Kim, Wan-Bae |
author_sort | Kim, Wan-Joon |
collection | PubMed |
description | We aimed to identify clinicopathological differences and factors affecting survival outcomes of stage T2a and T2b gallbladder cancer (GBC) and validate the oncological benefits of regional lymphadenectomy and hepatic resection in these patients. This single-center study enrolled patients who were diagnosed with pathologically confirmed T2 GBC and underwent curative resection between January 1995 and December 2017. Eighty-two patients with T2a and 50 with T2b GBCs were identified, and clinical information was retrospectively collected from medical records and analyzed. Five-year overall survival rates were 96.8% and 80.7% in T2a and T2b groups, respectively (P = .007). Three- and 5-year survival rates among all patients with T2 GBC without and with lymph node metastasis were 97.2% and 94.4% and 81.3% and 81.3%, respectively (P = .029). There was no difference in survival rates between the 2 groups according to whether hepatic resection was performed (P = .320). However, in the T2b group, those who underwent hepatic resection demonstrated a better survival rate than those who did not (P = .029). The T2b group had more multiple recurrence patterns than the T2a group, and the lymph nodes were the most common site in both groups. Multivariate analysis revealed that lymph node metastasis, vascular invasion, and tumor location were significant independent prognostic factors. Hepatic resection was not always necessary in patients with peritoneal-side GBC. Considering clinicopathological features and recurrence patterns, a systematic treatment plan, including radical resection and adjuvant treatment, should be established for hepatic-side GBC. |
format | Online Article Text |
id | pubmed-7133080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71330802020-04-13 Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location Kim, Wan-Joon Lim, Tae-Wan Park, Pyoung-Jae Choi, Sae-Byeol Kim, Wan-Bae Cancer Control Research Article We aimed to identify clinicopathological differences and factors affecting survival outcomes of stage T2a and T2b gallbladder cancer (GBC) and validate the oncological benefits of regional lymphadenectomy and hepatic resection in these patients. This single-center study enrolled patients who were diagnosed with pathologically confirmed T2 GBC and underwent curative resection between January 1995 and December 2017. Eighty-two patients with T2a and 50 with T2b GBCs were identified, and clinical information was retrospectively collected from medical records and analyzed. Five-year overall survival rates were 96.8% and 80.7% in T2a and T2b groups, respectively (P = .007). Three- and 5-year survival rates among all patients with T2 GBC without and with lymph node metastasis were 97.2% and 94.4% and 81.3% and 81.3%, respectively (P = .029). There was no difference in survival rates between the 2 groups according to whether hepatic resection was performed (P = .320). However, in the T2b group, those who underwent hepatic resection demonstrated a better survival rate than those who did not (P = .029). The T2b group had more multiple recurrence patterns than the T2a group, and the lymph nodes were the most common site in both groups. Multivariate analysis revealed that lymph node metastasis, vascular invasion, and tumor location were significant independent prognostic factors. Hepatic resection was not always necessary in patients with peritoneal-side GBC. Considering clinicopathological features and recurrence patterns, a systematic treatment plan, including radical resection and adjuvant treatment, should be established for hepatic-side GBC. SAGE Publications 2020-04-01 /pmc/articles/PMC7133080/ /pubmed/32233806 http://dx.doi.org/10.1177/1073274820915514 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Kim, Wan-Joon Lim, Tae-Wan Park, Pyoung-Jae Choi, Sae-Byeol Kim, Wan-Bae Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title | Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title_full | Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title_fullStr | Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title_full_unstemmed | Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title_short | Clinicopathological Differences in T2 Gallbladder Cancer According to Tumor Location |
title_sort | clinicopathological differences in t2 gallbladder cancer according to tumor location |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133080/ https://www.ncbi.nlm.nih.gov/pubmed/32233806 http://dx.doi.org/10.1177/1073274820915514 |
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