Literature DB >> 22669398

Microsatellite instability is associated with a better prognosis for gastric cancer patients after curative surgery.

Wen-Liang Fang1, Shih-Ching Chang, Yuan-Tzu Lan, Kuo-Hung Huang, Jen-Hao Chen, Su-Shun Lo, Mao-Chih Hsieh, Anna Fen-Yau Li, Chew-Wun Wu, Shih-Hwa Chiou.   

Abstract

BACKGROUND: Microsatellite instability (MSI) is one of the leading mechanisms for the carcinogenesis of gastric cancer. Its prognostic value is controversial.
METHODS: Between May 1988 and Oct 2003, a total of 214 gastric cancer patients undergoing curative surgery were enrolled, and their MSI statuses were classified as MSI-H (high) or MSI-L/S (low/stable). The clinicopathologic characteristics of MSI-H and MSI-L/S gastric cancers were compared.
RESULTS: The MSI-H tumors accounted for 11.7 % (n = 25) of the 214 total gastric cancers. Although not statistically significant, the MSI-H gastric cancers were more frequently located in the lower third of the stomach (64 % vs. 49.2 %) and were more often the intestinal type (72 % vs. 61.4 %) compared to the MSI-L/S gastric cancers. The MSI-H gastric cancers had a significantly better 5-year overall survival (OS) rate (68 % vs. 47.6 %, p = 0.030) and a trend of a better 3-year disease-free survival rate (71.8 % vs. 55.2 %, p = 0.076) compared to the MSI-L/S gastric cancers. A multivariate analysis revealed that pathologic TNM stage and MSI status were the independent prognostic factors for OS after curative surgery.
CONCLUSIONS: Compared to MSI-L/S tumors, MSI-H tumors are associated with a better OS rate for gastric cancer patients after R0 resection.

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Year:  2012        PMID: 22669398     DOI: 10.1007/s00268-012-1652-7

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  40 in total

1.  The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability.

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2.  Differences in genomic instability between intestinal- and diffuse-type gastric cancer.

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4.  Chemosensitivity and survival in gastric cancer patients with microsatellite instability.

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7.  Microsatellite instability-associated mutations associate preferentially with the intestinal type of primary gastric carcinomas in a high-risk population.

Authors:  Y J Chung; J M Song; J Y Lee; Y T Jung; E J Seo; S W Choi; M G Rhyu
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Review 9.  Microsatellite instability in colorectal cancer.

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Authors:  Rodrigo Oliva Perez; Carlos Eduardo Jacob; Fabricio L'ofreddo D'Ottaviano; Conrado Alvarenga; Adriana Safatle Ribeiro; Ulysses Ribeiro; Cláudio José Caldas Bresciani; Bruno Zilberstein; José Eduardo Krieger; Angelita Habr-Gama; Joaquim José Gama-Rodrigues
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  35 in total

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2.  Molecular classification and precision therapy of cancer: immune checkpoint inhibitors.

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5.  Mismatch repair deficiency, chemotherapy and survival for resectable gastric cancer: an observational study from the German staR cohort and a meta-analysis.

Authors:  J Schumacher; P Malfertheiner; M Venerito; T Stolze; S Franke; J Haybaeck; M Moehler; P P Grimminger; H Lang; W Roth; I Gockel; N Kreuser; H Bläker; C Wittekind; F Lordick; M Vieth; L Veits; O Waidmann; P Lingohr; U Peitz; C Schildberg; M Kruschewski; N Vassos; E Goni; C J Bruns; K Ridwelski; S Wolff; H Lippert
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Review 8.  Molecular alterations in gastric cancer with special reference to the early-onset subtype.

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Review 9.  Perspectives on new biomarkers in gastric cancer: diagnostic and prognostic applications.

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10.  Molecular and survival differences between familial and sporadic gastric cancers.

Authors:  Wen-Liang Fang; Shih-Ching Chang; Yuan-Tzu Lan; Kuo-Hung Huang; Su-Shun Lo; Anna Fen-Yau Li; Chin-Wen Chi; Chew-Wun Wu; Shih-Hwa Chiou
Journal:  Biomed Res Int       Date:  2013-03-05       Impact factor: 3.411

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