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Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review

Gastric cancer is a common digestive tract tumor and the second most prevalent cancer. The prognosis of advanced gastric cancer is poor. Conversion therapy can reduce tumor burden, downgrade tumor, and increase the possibility of complete resection, thus prolonging the survival time of patients with...

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Autores principales: Jiang, Dingyi, Xu, Yunyun, Chen, Yunwang, Jiang, Jiahong, Wang, Mingxing, Yang, Min, Chen, Zheling, Yang, Liu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381218/
https://www.ncbi.nlm.nih.gov/pubmed/32765260
http://dx.doi.org/10.3389/fphar.2020.01027
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author Jiang, Dingyi
Xu, Yunyun
Chen, Yunwang
Jiang, Jiahong
Wang, Mingxing
Yang, Min
Chen, Zheling
Yang, Liu
author_facet Jiang, Dingyi
Xu, Yunyun
Chen, Yunwang
Jiang, Jiahong
Wang, Mingxing
Yang, Min
Chen, Zheling
Yang, Liu
author_sort Jiang, Dingyi
collection PubMed
description Gastric cancer is a common digestive tract tumor and the second most prevalent cancer. The prognosis of advanced gastric cancer is poor. Conversion therapy can reduce tumor burden, downgrade tumor, and increase the possibility of complete resection, thus prolonging the survival time of patients with gastric cancer. In conversion therapy, chemotherapy and targeted therapy are the main methods of medical treatment, which can control tumor growth and recurrence. As an antiangiogenic targeted drug, apatinib is widely used in the third-line treatment of advanced gastric cancer. Recent studies have shown that it may be of great help in rapid reduction of tumor stage and improvement of prognosis in conversion therapy. This study reported three cases of gastric cancer complicated with multiple abdominal and retroperitoneal lymph node metastases. After receiving apatinib combined with SOX regimen for four cycles, computed tomography showed that the focus and lymph node metastasis were reduced after treatment, and primary tumors were resected. Postoperative pathology result showed that the patients got R0 resection. After radical surgery, the maintenance therapy including apatinib was given. The progression-free survival time was more than 10 months. Apatinib combined with SOX regimen as a conversion therapy for advanced gastric adenocarcinoma increases the possibility of successful surgical resection, which might prolong the survival time of patients.
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spelling pubmed-73812182020-08-05 Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review Jiang, Dingyi Xu, Yunyun Chen, Yunwang Jiang, Jiahong Wang, Mingxing Yang, Min Chen, Zheling Yang, Liu Front Pharmacol Pharmacology Gastric cancer is a common digestive tract tumor and the second most prevalent cancer. The prognosis of advanced gastric cancer is poor. Conversion therapy can reduce tumor burden, downgrade tumor, and increase the possibility of complete resection, thus prolonging the survival time of patients with gastric cancer. In conversion therapy, chemotherapy and targeted therapy are the main methods of medical treatment, which can control tumor growth and recurrence. As an antiangiogenic targeted drug, apatinib is widely used in the third-line treatment of advanced gastric cancer. Recent studies have shown that it may be of great help in rapid reduction of tumor stage and improvement of prognosis in conversion therapy. This study reported three cases of gastric cancer complicated with multiple abdominal and retroperitoneal lymph node metastases. After receiving apatinib combined with SOX regimen for four cycles, computed tomography showed that the focus and lymph node metastasis were reduced after treatment, and primary tumors were resected. Postoperative pathology result showed that the patients got R0 resection. After radical surgery, the maintenance therapy including apatinib was given. The progression-free survival time was more than 10 months. Apatinib combined with SOX regimen as a conversion therapy for advanced gastric adenocarcinoma increases the possibility of successful surgical resection, which might prolong the survival time of patients. Frontiers Media S.A. 2020-07-14 /pmc/articles/PMC7381218/ /pubmed/32765260 http://dx.doi.org/10.3389/fphar.2020.01027 Text en Copyright © 2020 Jiang, Xu, Chen, Jiang, Wang, Yang, Chen and Yang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Jiang, Dingyi
Xu, Yunyun
Chen, Yunwang
Jiang, Jiahong
Wang, Mingxing
Yang, Min
Chen, Zheling
Yang, Liu
Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title_full Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title_fullStr Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title_full_unstemmed Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title_short Apatinib Combined With SOX Regimen in Conversion Treatment of Advanced Gastric Cancer: A Case Series and Literature Review
title_sort apatinib combined with sox regimen in conversion treatment of advanced gastric cancer: a case series and literature review
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381218/
https://www.ncbi.nlm.nih.gov/pubmed/32765260
http://dx.doi.org/10.3389/fphar.2020.01027
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