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Ki-67 labeling index as a prognostic marker in advanced stomach cancer

PURPOSE: Proliferation marker Ki-67 is widely used in cancer prognosis prediction. We tried to investigate the role of Ki-67 as a prognostic factor in stomach cancer after surgery in this study. METHODS: We retrospectively evaluated 251 patients who underwent curative resection for gastric cancer fr...

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Autores principales: Seo, Sang Hyuk, Kim, Kwang Hee, Oh, Sang Hoon, Choi, Yunseon, Ahn, Ki Jung, Lee, Ji Young, Lee, Sang Min, Park, Jisun, Kim, Woo Gyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306504/
https://www.ncbi.nlm.nih.gov/pubmed/30603631
http://dx.doi.org/10.4174/astr.2019.96.1.27
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author Seo, Sang Hyuk
Kim, Kwang Hee
Oh, Sang Hoon
Choi, Yunseon
Ahn, Ki Jung
Lee, Ji Young
Lee, Sang Min
Park, Jisun
Kim, Woo Gyeong
author_facet Seo, Sang Hyuk
Kim, Kwang Hee
Oh, Sang Hoon
Choi, Yunseon
Ahn, Ki Jung
Lee, Ji Young
Lee, Sang Min
Park, Jisun
Kim, Woo Gyeong
author_sort Seo, Sang Hyuk
collection PubMed
description PURPOSE: Proliferation marker Ki-67 is widely used in cancer prognosis prediction. We tried to investigate the role of Ki-67 as a prognostic factor in stomach cancer after surgery in this study. METHODS: We retrospectively evaluated 251 patients who underwent curative resection for gastric cancer from 2010 to 2015. In pathologic examination, Ki-67 labeling index was defined as the percentage of Ki-67 antigen positive cells. Prognostic significance of Ki-67 for gastric cancer was evaluated. Disease-free survival (DFS) was assessed as a primary end-point. RESULTS: The median follow-up period was 28.0 months. Thirty-one patients (12.4%) showed Ki-67 labeling index (LI) lower than 25%. Sixty-eight patients (26.6%) showed recurrence during follow-up period. Recurrence was associated with Ki-67 LI level (≤25%, P = 0.016), and lymph node metastasis status (P = 0.002). High Ki-67 LI level (>25%) was also related to p53 positivity (P < 0.001) and poorly cohesive type (P = 0.002). The 3-year DFS was 69.4%. Low Ki-67 LI level (≤25%) was related with low DFS (47.6% vs. 72.6%, P = 0.016). T stage (P < 0.001), N stage (P = 0.006), lymphovascular invasion (P = 0.010), and neuronal invasion (P = 0.001) also affected the DFS. In addition, T stage (P = 0.03) and Ki-67 LI (P = 0.035) were independent prognostic factors for DFS. In patients treated with adjuvant chemotherapy (n = 239, 93.4%), low Ki-67 (≤25%) was a poor prognostic factor for DFS (P = 0.013). CONCLUSION: Low Ki-67 LI predicts high rate of progression and low DFS of stomach cancer. Ki-67 LI can be a predictive marker in resected stomach cancer treated with surgery and adjuvant chemotherapy.
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spelling pubmed-63065042019-01-03 Ki-67 labeling index as a prognostic marker in advanced stomach cancer Seo, Sang Hyuk Kim, Kwang Hee Oh, Sang Hoon Choi, Yunseon Ahn, Ki Jung Lee, Ji Young Lee, Sang Min Park, Jisun Kim, Woo Gyeong Ann Surg Treat Res Original Article PURPOSE: Proliferation marker Ki-67 is widely used in cancer prognosis prediction. We tried to investigate the role of Ki-67 as a prognostic factor in stomach cancer after surgery in this study. METHODS: We retrospectively evaluated 251 patients who underwent curative resection for gastric cancer from 2010 to 2015. In pathologic examination, Ki-67 labeling index was defined as the percentage of Ki-67 antigen positive cells. Prognostic significance of Ki-67 for gastric cancer was evaluated. Disease-free survival (DFS) was assessed as a primary end-point. RESULTS: The median follow-up period was 28.0 months. Thirty-one patients (12.4%) showed Ki-67 labeling index (LI) lower than 25%. Sixty-eight patients (26.6%) showed recurrence during follow-up period. Recurrence was associated with Ki-67 LI level (≤25%, P = 0.016), and lymph node metastasis status (P = 0.002). High Ki-67 LI level (>25%) was also related to p53 positivity (P < 0.001) and poorly cohesive type (P = 0.002). The 3-year DFS was 69.4%. Low Ki-67 LI level (≤25%) was related with low DFS (47.6% vs. 72.6%, P = 0.016). T stage (P < 0.001), N stage (P = 0.006), lymphovascular invasion (P = 0.010), and neuronal invasion (P = 0.001) also affected the DFS. In addition, T stage (P = 0.03) and Ki-67 LI (P = 0.035) were independent prognostic factors for DFS. In patients treated with adjuvant chemotherapy (n = 239, 93.4%), low Ki-67 (≤25%) was a poor prognostic factor for DFS (P = 0.013). CONCLUSION: Low Ki-67 LI predicts high rate of progression and low DFS of stomach cancer. Ki-67 LI can be a predictive marker in resected stomach cancer treated with surgery and adjuvant chemotherapy. The Korean Surgical Society 2019-01 2018-12-26 /pmc/articles/PMC6306504/ /pubmed/30603631 http://dx.doi.org/10.4174/astr.2019.96.1.27 Text en Copyright © 2019, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/4.0/ Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Seo, Sang Hyuk
Kim, Kwang Hee
Oh, Sang Hoon
Choi, Yunseon
Ahn, Ki Jung
Lee, Ji Young
Lee, Sang Min
Park, Jisun
Kim, Woo Gyeong
Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title_full Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title_fullStr Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title_full_unstemmed Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title_short Ki-67 labeling index as a prognostic marker in advanced stomach cancer
title_sort ki-67 labeling index as a prognostic marker in advanced stomach cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306504/
https://www.ncbi.nlm.nih.gov/pubmed/30603631
http://dx.doi.org/10.4174/astr.2019.96.1.27
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