AI Article Synopsis

  • DNA mismatch repair is believed to significantly influence the progression and outcomes of colorectal cancer, but its exact prognostic value remains unclear.
  • A systematic review of 21 studies assessed the relationship between mismatch repair deficiency and patient survival, finding that those with such deficiencies had lower overall and disease-free survival rates.
  • The analysis revealed that mismatch repair deficiency correlates with better prognosis in both Asian and Western populations, suggesting its potential as a valuable prognostic marker in colorectal cancer patients.

Article Abstract

DNA mismatch repair was proposed to play a pivotal role in the development and prognosis of colorectal cancer. However, the prognostic value of mismatch repair on colorectal cancer is still unknown. The PubMed, EMBASE, and Cochrane Central Register of Controlled Trials databases were searched. The articles about mismatch repair (including hMLH1, hMSH2, hMSH3, hMSH6, hPMSH1, and hPMSH2) deficiency for the prognosis of patients with colorectal cancer were included in the study. The hazard ratio and its 95% confidence interval were used to measure the impact of mismatch repair deficiency on survival time. Twenty-one articles were included. The combined hazard ratio for mismatch repair deficiency on overall survival was 0.59 (95% confidence interval: 0.50-0.69) and that on disease-free survival was 0.57 (95% confidence interval: 0.43-0.75). In subgroup analysis, there were a significant association between overall survival and mismatch repair deficiency in Asian studies (hazard ratio: 0.67; 95% confidence interval: 0.50-0.91) and Western studies (hazard ratio: 0.56; 95% confidence interval: 0.46-0.67). For disease-free survival, the hazard ratios in Asian studies and Western studies were 0.55 (95% confidence interval: 0.38-0.81) and 0.62 (95% confidence interval: 0.50-0.78), respectively. Our meta-analysis indicated that mismatch repair could be used to evaluate the prognosis of patients with colorectal cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259062PMC
http://dx.doi.org/10.1177/1533033818808507DOI Listing

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