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Prediction Model for Gastric Cancer With DNA Mismatch Repair Deficiency.

AbstractBACKGROUND/AIM:
DNA mismatch repair (MMR) deficiency has received increasing attention as a biomarker of anti-PD-1 treatments of solid tumors including gastric cancer (GC). However, efficient screening has not been established.
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.
AuthorsOkihide Suzuki, Tatsuro Yamaguchi, Minoru Fukuchi, Erito Mochiki, Tomio Arai, Kiwamu Akagi, Hideyuki Ishida
JournalAnticancer research (Anticancer Res) Vol. 41 Issue 2 Pg. 975-982 (Feb 2021) ISSN: 1791-7530 [Electronic] Greece
PMID33517304 (Publication Type: Journal Article)
CopyrightCopyright © 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
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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