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      Evaluation of the Eighth Edition of the American Joint Committee on Cancer TNM Staging System for Gastric Cancer: An Analysis of 7371 Patients in the SEER Database

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          Abstract

          Objective

          To investigate the validity of the 8 th edition of the American Joint Committee on Cancer (AJCC) TNM staging system for gastric cancer.

          Methods

          The clinicopathologic data of 7371 patients who were diagnosed with gastric cancer and had 16 or more involved lymph nodes (LNs) were retrieved from the Surveillance, Epidemiology, and End Results (SEER) database and retrospectively reviewed.

          Results

          Stage migration occurred primarily during stage III between the 7 th and 8 th edition TNM staging systems. Stages IIIB and IIIC in the 7 th edition staging system were divided in the 8 th edition and had obvious differences in survival rates (both P < 0.001). The 8 th edition TNM stages IIIC and IV showed similar survival rates ( P = 0.101). The prognosis of patients with T4aN3bM0 was not different from that of patients with TxNxM1 ( P = 0.433), while the prognosis of patients with T4bN3bM0 was significantly poorer than that of patients with TxNxM1 ( P = 0.008). A revised TNM system with both T4aN3bM0 and T4bN3bM0 incorporated into stage IV was proposed. Multivariable regression analysis showed that the revised TNM system, but not the 7 th and 8 th editions, was an independent factor for disease-specific survival (DSS) in the third step of the analysis. Further analyses revealed that the revised TNM system had superior discriminatory ability to the 8 th edition staging system, which was also an improvement over the 7 th edition staging system.

          Conclusion

          The 8 th edition of the AJCC TNM staging system is superior to the 7 th edition for predicting the DSS rates of gastric cancer patients. However, for better prognostic stratification, it might be more suitable for T4aN3bM0/T4bN3bM0 to be incorporated into stage IV in the 8 th edition TNM staging system.

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          Most cited references17

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          Global burden of gastric cancer attributable to Helicobacter pylori.

          We previously estimated that 660,000 cases of cancer in the year 2008 were attributable to the bacterium Helicobacter pylori (H. pylori), corresponding to 5.2% of the 12.7 million total cancer cases that occurred worldwide. In recent years, evidence has accumulated that immunoblot (western blot) is more sensitive for detection of anti-H. pylori antibodies than ELISA, the detection method used in our previous analysis. The purpose of this short report is to update the attributable fraction (AF) estimate for H. pylori after briefly reviewing new evidence, and to reassess the global burden of cancer attributable to H. pylori. We therefore reviewed the literature for studies comparing the risk of developing non-cardia gastric cancer (NCGC) in cases and controls, using both ELISA and multiple antigen immunoblot for detection of H. pylori. The results from prospective studies were combined, and the new pooled estimates were applied to the calculation of the AF for H. pylori in NCGC, then to the burden of infection-related cancers worldwide. Using the immunoblot-based data, the worldwide AF for H. pylori in NCGC increased from 74.7% to 89.0%. This implies approximately 120,000 additional cases of NCGC attributable to H. pylori infection for a total of around 780,000 cases (6.2% instead of 5.2% of all cancers). These updated estimates reinforce the role of H. pylori as a major cause of cancer.
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            Gastric Adenocarcinoma : Review and Considerations for Future Directions

            This update reviews the epidemiology and surgical management, and the controversies of gastric adenocarcinoma. We provide the relevance of outcome data to surgical decision-making and discuss the application of gene-expression analysis to clinical practice. Gastric cancer mortality rates have remained relatively unchanged over the past 30 years, and gastric cancer continues to be one of the leading causes of cancer-related death. Well-conducted studies have stimulated changes to surgical decision-making and technique. Microarray studies linked to predictive outcome models are poised to advance our understanding of the biologic behavior of gastric cancer and improve surgical management and outcome. We performed a review of the English gastric adenocarcinoma medical literature (1980-2003). This review included epidemiology, pathology and staging, surgical management, issues and controversies in management, prognostic variables, and the application of outcome models to gastric cancer. The results of DNA microarray analysis in various cancers and its predictive abilities in gastric cancer are considered. Prognostic studies have provided valuable data to better the understanding of gastric cancer. These studies have contributed to improved surgical technique, more accurate pathologic characterization, and the identification of clinically useful prognostic markers. The application of microarray analysis linked to predictive models will provide a molecular understanding of the biology driving gastric cancer. Predictive models generate important information allowing a logical evolution in the surgical and pathologic understanding and therapy for gastric cancer. However, a greater understanding of the molecular changes associated with gastric cancer is needed to guide surgical and medical therapy.
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              Validation of the 8th Edition of the AJCC TNM Staging System for Gastric Cancer using the National Cancer Database.

              The 8th edition AJCC gastric cancer staging manual was refined using Japanese and Korean data from the International Gastric Cancer Association (IGCA). This study evaluated the eighth edition's validity for U.S.
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                Author and article information

                Contributors
                Journal
                Gastroenterol Res Pract
                Gastroenterol Res Pract
                GRP
                Gastroenterology Research and Practice
                Hindawi
                1687-6121
                1687-630X
                2019
                14 April 2019
                : 2019
                : 6294382
                Affiliations
                1Department of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, Fujian Province, China
                2Department of General Surgery, Fujian Medical University Union Hospital, Fuzhou, Fujian Province, China
                3Key Laboratory of Ministry of Education of Gastrointestinal Cancer, Fujian Medical University, Fuzhou, Fujian Province, China
                4Fujian Key Laboratory of Tumor Microbiology, Fujian Medical University, Fuzhou, Fujian Province, China
                Author notes

                Academic Editor: Giuseppe Nigri

                Author information
                http://orcid.org/0000-0003-0157-5167
                http://orcid.org/0000-0002-0019-885X
                Article
                10.1155/2019/6294382
                6487090
                31097961
                6ec7295f-20c2-4e9a-84fa-2be5db20f3c7
                Copyright © 2019 Long-Long Cao et al.

                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.

                History
                : 27 September 2018
                : 18 December 2018
                : 15 January 2019
                Funding
                Funded by: Youth Research Project of Fujian Provincial Health and Family Planning Commission
                Award ID: 2011532#
                Funded by: Fujian Medical University
                Award ID: 2014MP022
                Award ID: 2016QH024
                Funded by: Scientific and Technological Innovation Joint Capital Projects of Fujian Province
                Award ID: 2016Y9031
                Categories
                Research Article

                Gastroenterology & Hepatology
                Gastroenterology & Hepatology

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