Literature DB >> 28053675

Ongoing problems concerning 7th TNM Staging System and Proposals for 8th TNM Staging System of Gastric Cancer.

Enver Ilhan1, Orhan Ureyen1, Ulvi Mehmet Meral2.   

Abstract

Because of different prognosis of gastric cancer patients with the same T and N stages, the impossibility of N3 staging in patients with fewer than 15 removed lymph nodes, and the presence of stage migration phenomenon, the 6th edition TNM Staging System for gastric cancer was updated to the 7th edition TNM staging system in 2009. Despite some opposing views, the superiority of the 7th edition TNM staging system compared to the 6th has been demonstrated in many studies. However, there are doubts about the 7th edition that it will reduce the stage migration phenomenon. The most important problem about the 7th TNM staging system is regarding subgroups N3a and N3b. The separation of N3 stage as N3a and N3b does not contribute to the TNM staging system. In conclusion, separate usage of N3a and N3b subgroups in the TNM staging system should be considered in the creation phase of the 8th edition.

Entities:  

Keywords:  N-ratio; N3a; N3b; TNM; gastric cancer

Year:  2016        PMID: 28053675      PMCID: PMC5209469          DOI: 10.5114/pg.2016.64069

Source DB:  PubMed          Journal:  Prz Gastroenterol        ISSN: 1895-5770


The tumor node metastasis (TNM) staging system is considered as the gold standard for staging gastric cancer as well as staging of other types of cancer. Because of different prognosis of gastric cancer patients with the same T and N stages, the impossibility of N3 staging in patients with fewer than 15 removed lymph nodes, and the presence of stage migration phenomenon, the 6th Edition American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) TNM Staging System for gastric cancer was updated to the 7th Edition UICC/AJCC TNM Staging System in 2009. In the 7th edition TNM staging system there are several major changes in T, N, and TNM staging systems (Tables I and II). In the 7th edition TNM staging system, greater than or equal to seven metastatic lymph nodes were classified as N3 stage. Furthermore, the component of stage IV including M0 was removed and IIIC was added to the TNM staging system with the components of T4aN3M0, T4bN2M0, and T4bN3M0. In addition, positive peritoneal cytology (CY+) was assessed as M 1 (stage IV) in the 7th edition TNM staging system. Moreover, gastroesophageal junction (GEJ) tumours such as Siewert type I and II were classified as oesophageal cancer, and Siewert III type tumors were classified as gastric cancers. All of these changes were thought to be effective in the evaluation of clinicopathological data and in minimising the stage migration phenomenon [1].
Table I

The comparison of T and N stages in 6th edition and 7th edition TNM staging systems

6th edition UICC/AJC TNM Staging System (2002)7th edition UICC/AJCC TNM Staging System (2009)
T1T1a – lamina propria, muscularis mucosa
T1T1b – submucosa
T2aT2 – muscularis propria
T2bT3 – subserosa
T3T4a – serosa invasion
T4T4b – adjacent organ invasion
N1N1 (1–2 lymph node metastasis)
N1N2 (3–6 lymph node metastasis)
N2N3a (7–15 lymph node metastasis)
N3N3b (16 and more lymph node metastasis)
Table II

The comparison of 6th edition and 7th edition TNM staging system

6th edition UICC/AJC TNM Staging System (2002)7th edition UICC/AJCC TNM Staging System (2009)
StageTNMStageTNM
0TisN0M00TisN0M0
IAT1N0M0IAT1N0M0
IBT1N1M0, T2N0M0IBT2N0M0, T1N1M0
IIT1N2M0, T2N1M0, T3N0M0IIAT3N0M0, T2N1M0, T1N2M0
IIIAT2N2M0, T3N1M0, T4N0M0IIBT4aN0M0, T3N1M0, T2N2M0, T1N3M0
IIIBT3N2M0IIIAT4aN1M0, T3N2M0, T2N3M0
IV (with M0)T1-3N3M0, T4N1-3M0IIIBT4bN0M0, T4bN1M0, T4aN2M0, T3N3M0
IV (with M1)Any T, any N, M1IIICT4bN2M0, T4bN3M0, T4aN3M0
IVAny T, any N, M1
The comparison of T and N stages in 6th edition and 7th edition TNM staging systems The comparison of 6th edition and 7th edition TNM staging system Despite some opposing views, the superiority of the 7th edition compared to the 6th has been demonstrated in many studies [2-4]. However, there are doubts about the 7th edition that it will reduce the stage migration phenomenon [5]. Therefore, the search for alternatives to the TNM staging system and proposals for modification of the system continues. One of them is a hypothetical classification based on the ratio between metastatic and examined lymph nodes (N-ratio). Because both positive lymph nodes and examined nodes are its main components, it has been suggested that the N-ratio staging system is effective in precluding stage migration and determining the prognosis, and it can be used instead of N-staging [6, 7]. Another important point about the 7th edition TNM staging system is regarding subgroups N3a and N3b. Although T4a and T4b stages correspond to different stages in the 7th edition TNM staging system, separated concepts of N3a and N3b stages correspond to relevant stages as the only N stage as N3. In this case, the separation of N3 stage as N3a and N3b does not contribute to the TNM staging system. Yeh et al. [8] evaluated 884 N3 positive patients for N3a and N3b subtypes, clinico-pathological findings, and surgical outcomes. The findings of this study showed that the survival of: a) T1-3N3aM0 patients is similar to stage IIIB patients, b) T1-3N3bM0 patients is similar to stage III C patients, c) T4aN3bM0 patients is lower than stage IIIC and higher than stage IV patients, and d) T4bN3bM0 patients is similar to stage IV patients. Based on these findings, the authors suggested modification of the 7th edition TNM staging system to classify T1-3N3aM0 as sage IIIB, T1-3N3bM0 as stage IIIC, T4aN3bM0 as stage IIID, and T4bN3bM0 as stage IV. In a study of Ahn et al. [4] including 9998 gastric cancer patients, the researchers announced the superiority of the 7th TNM staging system over the 6th TNM staging system in terms of prognosis, especially for T2/T3 and N1/N2 tumours, but they indicated that further studies are needed for N3a and N3b subclassification. Most recently, Sano et al. [9] published the results of the International Gastric Cancer Association (IGCA) Project study. Fifteen countries and 53 institutions participated in the study. The clinical and pathological data of 25,441 patients who underwent curative gastrectomy between 2000 and 2004 were evaluated retrospectively. Of the participating patients, 84.8% were from Japan and South Korea. N3a and N3b subgroups had different results in terms of 5-year survival rate. The authors suggested a new staging system (IGCA Proposal Staging System) for gastric cancer and Siewert type II-III EGJ tumours evaluating N3a and N3b subtypes separately. There are significant differences in the proposed staging system, especially in stage III subgroups. According to these results, the authors have noted the availability of the IGCA proposal staging system’s advantages compared to AJCC7 for both gastric and Siewert type II, and III EGJ tumours. They also suggested its usage for forthcoming TNM staging system of gastric cancer. In conclusion, separate usage of N3a and N3b subgroups in the TNM staging system should be considered in the creation phase of the 8th edition TNM staging system. In that case, however, evaluation failure of N3b sub-classification should occur in patients with fewer than 15 lymph nodes examined. We think this problem can be solved by acceptance of the suggestion “25 lymph nodes should be removed for extended lymphadenectomy” of the German Gastric Cancer Group [10] or the usage of a hypothetical N-ratio staging system.
  8 in total

1.  Adjustment of N stages of gastric cancer by the ratio between the metastatic and examined lymph nodes.

Authors:  Chan-Young Kim; Doo-Hyun Yang
Journal:  Ann Surg Oncol       Date:  2009-05-12       Impact factor: 5.344

2.  Evaluation of the seventh American Joint Committee on Cancer/International Union Against Cancer Classification of gastric adenocarcinoma in comparison with the sixth classification.

Authors:  Hye Seong Ahn; Hyuk-Joon Lee; Seokyung Hahn; Woo-Ho Kim; Kuhn Uk Lee; Takeshi Sano; Stephen B Edge; Han-Kwang Yang
Journal:  Cancer       Date:  2010-08-24       Impact factor: 6.860

3.  Proposal of a new stage grouping of gastric cancer for TNM classification: International Gastric Cancer Association staging project.

Authors:  Takeshi Sano; Daniel G Coit; Hyung Ho Kim; Franco Roviello; Paulo Kassab; Christian Wittekind; Yuko Yamamoto; Yasuo Ohashi
Journal:  Gastric Cancer       Date:  2016-02-20       Impact factor: 7.370

4.  Clinical implication of an insufficient number of examined lymph nodes after curative resection for gastric cancer.

Authors:  Taeil Son; Woo Jin Hyung; Joong Ho Lee; Yoo Min Kim; Hyoung-Il Kim; Ji Yeong An; Jae-Ho Cheong; Sung Hoon Noh
Journal:  Cancer       Date:  2012-03-13       Impact factor: 6.860

5.  Relevant prognostic factors in gastric cancer: ten-year results of the German Gastric Cancer Study.

Authors:  J R Siewert; K Böttcher; H J Stein; J D Roder
Journal:  Ann Surg       Date:  1998-10       Impact factor: 12.969

6.  The superiority of the seventh edition of the TNM classification depends on the overall survival of the patient cohort: comparative analysis of the sixth and seventh TNM editions in patients with gastric cancer from Japan and the United Kingdom.

Authors:  Tsutomu Hayashi; Takaki Yoshikawa; Kiran Bonam; Henry M Sue-Ling; Masataka Taguri; Satoshi Morita; Akira Tsuburaya; Jeremy D Hayden; Heike I Grabsch
Journal:  Cancer       Date:  2012-12-21       Impact factor: 6.860

7.  N3 subclassification incorporated into the final pathologic staging of gastric cancer: a modified system based on current AJCC staging.

Authors:  Chun-Nan Yeh; Shang-Yu Wang; Jun-Te Hsu; Kun-Chun Chiang; Chi-Tung Cheng; Chun-Yi Tsai; Yu-Yin Liu; Chien-Hung Liao; Keng-Hao Liu; Ta-Sen Yeh
Journal:  Medicine (Baltimore)       Date:  2015-02       Impact factor: 1.889

8.  Comparison of the 6th and 7th editions of the AJCC/UICC TNM staging system for gastric cancer focusing on the "N" parameter-related survival: the monoinstitutional NodUs Italian study.

Authors:  Luigi Marano; Virginia Boccardi; Bartolomeo Braccio; Giuseppe Esposito; Michele Grassia; Marianna Petrillo; Modestino Pezzella; Raffaele Porfidia; Gianmarco Reda; Angela Romano; Michele Schettino; Angelo Cosenza; Giuseppe Izzo; Natale Di Martino
Journal:  World J Surg Oncol       Date:  2015-07-16       Impact factor: 2.754

  8 in total
  7 in total

1.  Superiority of the 8th edition of the TNM staging system for predicting overall survival in gastric cancer: Comparative analysis of the 7th and 8th editions in a monoinstitutional cohort.

Authors:  Hao Wang; Weihong Guo; Yanfeng Hu; Tingyu Mou; Liying Zhao; Hao Chen; Tian Lin; Tuanjie Li; Jiang Yu; Hao Liu; Guoxin Li
Journal:  Mol Clin Oncol       Date:  2018-07-26

2.  Should Pyloric Lymph Nodes Be Dissected for Siewert Type II and III Adenocarcinoma of the Esophagogastric Junctions: Experience from a High-Volume Center in China.

Authors:  Huihua Cao; Marie Ooi; Zhan Yu; Qing Wang; Zhong Li; Qicheng Lu; Yugang Wu
Journal:  J Gastrointest Surg       Date:  2018-10-17       Impact factor: 3.452

3.  Development and validation of a survival model based on autophagy-associated genes for predicting prognosis of hepatocellular carcinoma.

Authors:  Wanli Yang; Liaoran Niu; Xinhui Zhao; Lili Duan; Yiding Li; Xiaoqian Wang; Yujie Zhang; Wei Zhou; Jinqiang Liu; Qingchuan Zhao; Yu Han; Daiming Fan; Liu Hong
Journal:  Am J Transl Res       Date:  2020-10-15       Impact factor: 4.060

4.  Expression of ALDH1A1 and CD133 is associated with the prognosis and effect of different chemotherapeutic regimens in gastric cancer.

Authors:  Wan-Ting Liu; Wen-Bo Liu; Min Gao; Yi-Yin Zhang; Kang-Sheng Gu
Journal:  Oncol Lett       Date:  2019-09-04       Impact factor: 2.967

5.  Comprehensive Analysis of the Expression and Prognosis for ITGBs: Identification of ITGB5 as a Biomarker of Poor Prognosis and Correlated with Immune Infiltrates in Gastric Cancer.

Authors:  Dongliang Liu; Shaojun Liu; Yu Fang; Liu Liu; Kongwang Hu
Journal:  Front Cell Dev Biol       Date:  2022-02-09

Review 6.  Revisiting the 8th AJCC system for gastric cancer: A review on validations, nomograms, lymph nodes impact, and proposed modifications.

Authors:  Geofrey Mahiki Mranda; Ying Xue; Xing-Guo Zhou; Wang Yu; Tian Wei; Zhi-Ping Xiang; Jun-Jian Liu; Yin-Lu Ding
Journal:  Ann Med Surg (Lond)       Date:  2022-02-25

7.  Co-Expression of LGR5 and CD133 Cancer Stem Cell Predicts a Poor Prognosis in Patients With Gastric Cancer.

Authors:  Wareeporn Wattanawongdon; Theeraya Simawaranon Bathpho; Taweesak Tongtawee
Journal:  Turk J Gastroenterol       Date:  2021-03       Impact factor: 1.852

  7 in total

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