Relationship between p53 status and response to chemotherapy in patients with gastric cancer: a meta-analysis

PLoS One. 2014 Apr 16;9(4):e95371. doi: 10.1371/journal.pone.0095371. eCollection 2014.

Abstract

Background: Previous studies have yielded conflicting results regarding the relationship between p53 status and response to chemotherapy in patients with gastric cancer. We therefore performed a meta-analysis to expound the relationship between p53 status and response to chemotherapy.

Methods/findings: Thirteen previously published eligible studies, including 564 cases, were identified and included in this meta-analysis. p53 positive status (high expression of p53 protein and/or a mutant p53 gene) was associated with improved response in gastric cancer patients who received chemotherapy (good response: risk ratio [RR] = 0.704; 95% confidence intervals [CI] = 0.550-0.903; P = 0.006). In further stratified analyses, association with a good response remained in the East Asian population (RR = 0.657; 95% CI = 0.488-0.884; P = 0.005), while in the European subgroup, patients with p53 positive status tended to have a good response to chemotherapy, although this did not reach statistical significance (RR = 0.828, 95% CI = 0.525-1.305; P = 0.417). As five studies used neoadjuvant chemotherapy (NCT) and one used neoadjuvant chemoradiotherapy (NCRT), we also analyzed these data, and found that p53 positive status was associated with a good response in gastric cancer patients who received chemotherapy-based neoadjuvant treatment (RR = 0.675, 95% CI = 0.463-0.985; P = 0.042).

Conclusion: This meta-analysis indicated that p53 status may be a useful predictive biomarker for response to chemotherapy in gastric cancer. Further prospective studies with larger sample sizes and better study designs are required to confirm our findings.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Asian People
  • Drug Monitoring
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Mutation
  • Neoadjuvant Therapy*
  • Prognosis
  • Stomach Neoplasms / drug therapy*
  • Stomach Neoplasms / ethnology
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology
  • Treatment Outcome
  • Tumor Suppressor Protein p53 / genetics*
  • Tumor Suppressor Protein p53 / metabolism
  • White People

Substances

  • Antineoplastic Agents
  • Tumor Suppressor Protein p53

Grants and funding

This work was supported by the National Natural Science Foundation (No. 81101677,81070423). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.