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GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial

Neoadjuvant chemotherapy (NCT) is a standard care for esophageal squamous cell carcinoma (ESCC), but the efficacy is unsatisfactory. Cancer stem cells (CSCs) play key roles in chemotherapy resistance. Gene amplified in squamous cell carcinoma 1 (GASC1) is a neoteric gene in stemness maintaining of E...

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Autores principales: Jia, Ruinuo, Mi, Youjia, Yuan, Xiang, Kong, Dejiu, Li, Wanying, Li, Ruonan, Wang, Bingbing, Zhu, Yafei, Kong, Jinyu, Ma, Zhikun, Li, Na, Mi, Qiangjian, Gao, Shegan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204099/
https://www.ncbi.nlm.nih.gov/pubmed/32411232
http://dx.doi.org/10.1155/2020/1607860
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author Jia, Ruinuo
Mi, Youjia
Yuan, Xiang
Kong, Dejiu
Li, Wanying
Li, Ruonan
Wang, Bingbing
Zhu, Yafei
Kong, Jinyu
Ma, Zhikun
Li, Na
Mi, Qiangjian
Gao, Shegan
author_facet Jia, Ruinuo
Mi, Youjia
Yuan, Xiang
Kong, Dejiu
Li, Wanying
Li, Ruonan
Wang, Bingbing
Zhu, Yafei
Kong, Jinyu
Ma, Zhikun
Li, Na
Mi, Qiangjian
Gao, Shegan
author_sort Jia, Ruinuo
collection PubMed
description Neoadjuvant chemotherapy (NCT) is a standard care for esophageal squamous cell carcinoma (ESCC), but the efficacy is unsatisfactory. Cancer stem cells (CSCs) play key roles in chemotherapy resistance. Gene amplified in squamous cell carcinoma 1 (GASC1) is a neoteric gene in stemness maintaining of ESCC. We aimed to reveal whether GASC1 could be a predictive biomarker for NCT in ESCC. ESCC patients (T2-4N0-2M0) were evaluated for GASC1 expression using immunohistochemical staining and classified as GASC1-low group (GLG) and GASC1-high group (GHG). NCT was delivered in two cycles and then the surgery was completed. Primary endpoints were tumor regression grade (TRG) and objective response rate (ORR); secondary endpoints were radical surgical resection (R0) rate and three-year overall survival (OS). 60 patients were eligible with evaluable outcomes: 24 in GHG and 36 in GLG. Between GHG and GLG, TRG1, TRG2, TRG3, and TRG4 were 0 : 16.7%, 20.8% : 41.7%, 58.3% : 36.1%, and 20.8% : 5.6%, respectively (P=0.006); ORR and R0 rate were 33.3% : 69.4% (P=0.006) and 75% : 94.4% (P=0.046), respectively; the median OS was 20 : 32 (months) (P=0.0356). No significant difference in the three-year OS was observed between GHG and GLG: 29.2% : 41.7% (P=0.24). Furthermore, the GASC1 expression level was associated with poor OS independent of other factors by univariate and multivariate analyses. Therefore, GASC1 might be a potential biomarker to predict NCT efficacy for ESCC.
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spelling pubmed-72040992020-05-14 GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial Jia, Ruinuo Mi, Youjia Yuan, Xiang Kong, Dejiu Li, Wanying Li, Ruonan Wang, Bingbing Zhu, Yafei Kong, Jinyu Ma, Zhikun Li, Na Mi, Qiangjian Gao, Shegan J Oncol Research Article Neoadjuvant chemotherapy (NCT) is a standard care for esophageal squamous cell carcinoma (ESCC), but the efficacy is unsatisfactory. Cancer stem cells (CSCs) play key roles in chemotherapy resistance. Gene amplified in squamous cell carcinoma 1 (GASC1) is a neoteric gene in stemness maintaining of ESCC. We aimed to reveal whether GASC1 could be a predictive biomarker for NCT in ESCC. ESCC patients (T2-4N0-2M0) were evaluated for GASC1 expression using immunohistochemical staining and classified as GASC1-low group (GLG) and GASC1-high group (GHG). NCT was delivered in two cycles and then the surgery was completed. Primary endpoints were tumor regression grade (TRG) and objective response rate (ORR); secondary endpoints were radical surgical resection (R0) rate and three-year overall survival (OS). 60 patients were eligible with evaluable outcomes: 24 in GHG and 36 in GLG. Between GHG and GLG, TRG1, TRG2, TRG3, and TRG4 were 0 : 16.7%, 20.8% : 41.7%, 58.3% : 36.1%, and 20.8% : 5.6%, respectively (P=0.006); ORR and R0 rate were 33.3% : 69.4% (P=0.006) and 75% : 94.4% (P=0.046), respectively; the median OS was 20 : 32 (months) (P=0.0356). No significant difference in the three-year OS was observed between GHG and GLG: 29.2% : 41.7% (P=0.24). Furthermore, the GASC1 expression level was associated with poor OS independent of other factors by univariate and multivariate analyses. Therefore, GASC1 might be a potential biomarker to predict NCT efficacy for ESCC. Hindawi 2020-01-30 /pmc/articles/PMC7204099/ /pubmed/32411232 http://dx.doi.org/10.1155/2020/1607860 Text en Copyright © 2020 Ruinuo Jia et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jia, Ruinuo
Mi, Youjia
Yuan, Xiang
Kong, Dejiu
Li, Wanying
Li, Ruonan
Wang, Bingbing
Zhu, Yafei
Kong, Jinyu
Ma, Zhikun
Li, Na
Mi, Qiangjian
Gao, Shegan
GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title_full GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title_fullStr GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title_full_unstemmed GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title_short GASC1-Adapted Neoadjuvant Chemotherapy for Resectable Esophageal Squamous Cell Carcinoma: A Prospective Clinical Biomarker Trial
title_sort gasc1-adapted neoadjuvant chemotherapy for resectable esophageal squamous cell carcinoma: a prospective clinical biomarker trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204099/
https://www.ncbi.nlm.nih.gov/pubmed/32411232
http://dx.doi.org/10.1155/2020/1607860
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