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Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer

PURPOSE: Microsatellite instability (MSI) status may affect the efficacy of adjuvant chemotherapy in gastric cancer. In this study, the clinical characteristics of MSI-high (MSI-H) gastric cancer and the predictive value of MSI-H for adjuvant chemotherapy in large cohorts of gastric cancer patients...

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Autores principales: Kim, Jin Won, Cho, Sung-Yup, Chae, Jeesoo, Kim, Ji-Won, Kim, Tae-Yong, Lee, Keun-Wook, Oh, Do-Youn, Bang, Yung-Jue, Im, Seock-Ah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577821/
https://www.ncbi.nlm.nih.gov/pubmed/32599979
http://dx.doi.org/10.4143/crt.2020.313
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author Kim, Jin Won
Cho, Sung-Yup
Chae, Jeesoo
Kim, Ji-Won
Kim, Tae-Yong
Lee, Keun-Wook
Oh, Do-Youn
Bang, Yung-Jue
Im, Seock-Ah
author_facet Kim, Jin Won
Cho, Sung-Yup
Chae, Jeesoo
Kim, Ji-Won
Kim, Tae-Yong
Lee, Keun-Wook
Oh, Do-Youn
Bang, Yung-Jue
Im, Seock-Ah
author_sort Kim, Jin Won
collection PubMed
description PURPOSE: Microsatellite instability (MSI) status may affect the efficacy of adjuvant chemotherapy in gastric cancer. In this study, the clinical characteristics of MSI-high (MSI-H) gastric cancer and the predictive value of MSI-H for adjuvant chemotherapy in large cohorts of gastric cancer patients were evaluated. MATERIAL AND METHODS: This study consisted of two cohorts. Cohort 1 included gastric cancer patients who received curative resection with pathologic stage IB-IIIC. Cohort 2 included patients with MSI-H gastric cancer who received curative resection with pathologic stage II/III. MSI was examined using two mononucleotide markers and three dinucleotide markers. RESULTS: Of 359 patients (cohort 1), 41 patients (11.4%) had MSI-H. MSI-H tumors were more frequently identified in older patients (p < 0.001), other histology than poorly cohesive, signet ring cell type (p=0.005), intestinal type (p=0.028), lower third tumor location (p=0.005), and absent perineural invasion (p=0.027). MSI-H status has a tendency of better disease-free survival (DFS) and overall survival (OS) in multivariable analyses (hazard ratio [HR], 0.4; p=0.059 and HR, 0.4; p=0.063, respectively). In the analysis of 162 MSI-H patients (cohort 2), adjuvant chemotherapy showed a significant benefit with respect to longer DFS and OS (p=0.047 and p=0.043, respectively). In multivariable analysis, adjuvant chemotherapy improved DFS (HR, 0.4; p=0.040). CONCLUSION: MSI-H gastric cancer had distinct clinicopathologic findings. Even in MSI-H gastric cancer of retrospective cohort, adjuvant chemotherapy could show a survival benefit, which was in contrast to previous prospective studies and should be investigated in a further prospective trial.
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spelling pubmed-75778212020-10-26 Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer Kim, Jin Won Cho, Sung-Yup Chae, Jeesoo Kim, Ji-Won Kim, Tae-Yong Lee, Keun-Wook Oh, Do-Youn Bang, Yung-Jue Im, Seock-Ah Cancer Res Treat Original Article PURPOSE: Microsatellite instability (MSI) status may affect the efficacy of adjuvant chemotherapy in gastric cancer. In this study, the clinical characteristics of MSI-high (MSI-H) gastric cancer and the predictive value of MSI-H for adjuvant chemotherapy in large cohorts of gastric cancer patients were evaluated. MATERIAL AND METHODS: This study consisted of two cohorts. Cohort 1 included gastric cancer patients who received curative resection with pathologic stage IB-IIIC. Cohort 2 included patients with MSI-H gastric cancer who received curative resection with pathologic stage II/III. MSI was examined using two mononucleotide markers and three dinucleotide markers. RESULTS: Of 359 patients (cohort 1), 41 patients (11.4%) had MSI-H. MSI-H tumors were more frequently identified in older patients (p < 0.001), other histology than poorly cohesive, signet ring cell type (p=0.005), intestinal type (p=0.028), lower third tumor location (p=0.005), and absent perineural invasion (p=0.027). MSI-H status has a tendency of better disease-free survival (DFS) and overall survival (OS) in multivariable analyses (hazard ratio [HR], 0.4; p=0.059 and HR, 0.4; p=0.063, respectively). In the analysis of 162 MSI-H patients (cohort 2), adjuvant chemotherapy showed a significant benefit with respect to longer DFS and OS (p=0.047 and p=0.043, respectively). In multivariable analysis, adjuvant chemotherapy improved DFS (HR, 0.4; p=0.040). CONCLUSION: MSI-H gastric cancer had distinct clinicopathologic findings. Even in MSI-H gastric cancer of retrospective cohort, adjuvant chemotherapy could show a survival benefit, which was in contrast to previous prospective studies and should be investigated in a further prospective trial. Korean Cancer Association 2020-10 2020-06-11 /pmc/articles/PMC7577821/ /pubmed/32599979 http://dx.doi.org/10.4143/crt.2020.313 Text en Copyright © 2020 by the Korean Cancer Association This is an Open Access article 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
Kim, Jin Won
Cho, Sung-Yup
Chae, Jeesoo
Kim, Ji-Won
Kim, Tae-Yong
Lee, Keun-Wook
Oh, Do-Youn
Bang, Yung-Jue
Im, Seock-Ah
Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title_full Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title_fullStr Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title_full_unstemmed Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title_short Adjuvant Chemotherapy in Microsatellite Instability–High Gastric Cancer
title_sort adjuvant chemotherapy in microsatellite instability–high gastric cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577821/
https://www.ncbi.nlm.nih.gov/pubmed/32599979
http://dx.doi.org/10.4143/crt.2020.313
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