Abstract | BACKGROUND/AIM: PATIENTS AND METHODS: A total of 513 patients were tested for the expression of MMR proteins by immunohistochemistry to identify MMR deficient GC. Development of a prediction model was attempted using the common clinicopathological features. RESULTS: In total, 11% (57/513) of the patients showed loss of expression of either one or more MMR proteins (MMR protein deficiency; MMR-D). Multivariate analysis demonstrated that age (≥70 years), sex (female), tumor location (lower 1/3), depth invasion (low, T1/T2/T3), and absence of distant metastasis were significantly independent predictive factors of MMR-D GCs. The MMR-D GC probability estimated by the prediction model ranged from 0.4% to 62.2%, and the area under the curve of the receiver operating characteristics curve was 0.82 (95% confidence interval=0.75-0.87). CONCLUSION: Our prediction model can sufficiently and efficiently identify MMR-D GCs using clinical features.
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Authors | Okihide Suzuki, Tatsuro Yamaguchi, Minoru Fukuchi, Erito Mochiki, Tomio Arai, Kiwamu Akagi, Hideyuki Ishida |
Journal | Anticancer research
(Anticancer Res)
Vol. 41
Issue 2
Pg. 975-982
(Feb 2021)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 33517304
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Biomarkers, Tumor
- DNA-Binding Proteins
- G-T mismatch-binding protein
- MLH1 protein, human
- PMS2 protein, human
- Mismatch Repair Endonuclease PMS2
- MutL Protein Homolog 1
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Area Under Curve
- Biomarkers, Tumor
(metabolism)
- DNA Mismatch Repair
- DNA-Binding Proteins
(deficiency)
- Female
- Humans
- Male
- Middle Aged
- Mismatch Repair Endonuclease PMS2
(deficiency)
- MutL Protein Homolog 1
(deficiency)
- Neoplasm Grading
- Neoplasm Invasiveness
- Sex Characteristics
- Stomach Neoplasms
(metabolism, pathology)
- Tumor Burden
- Young Adult
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