The impact of GGH -401C>T polymorphism on cisplatin-based chemoradiotherapy response and survival in cervical cancer

Gene. 2013 Jan 10;512(2):247-50. doi: 10.1016/j.gene.2012.10.038. Epub 2012 Oct 26.

Abstract

Aims: Cervical cancer is the third most frequent cancer in women worldwide, mostly treated with cisplatin-based chemoradiotherapy. Since it is known that folate metabolism might interfere with cisplatin effectiveness, we intended to study the influence of the Gamma Glutamyl Hydrolase -401C>T polymorphism in treatment response in cervical cancer.

Methods: We retrospectively reviewed the clinical data of 167 patients with bulky cervical cancer submitted to cisplatin-based chemoradiotherapy. The genotypes of GGH -401C>T SNP were determined by real-time PCR and statistical analysis was performed by χ(2) test and survival analysis.

Results: The genotypes of GGH-401C>T were significantly associated with the response to platinum-based chemoradiotherapy. Treatment response was higher in patients carrying the CC genotype, who presented a significant increased chance of treatment response (survival time in months/genotype: 91 for CC Vs 72 for CT/TT; p=0.035, log rank test). A Cox regression analysis accordingly showed that the presence of the T allele was significantly linked to a worse treatment response (HR=3.036; CI 95% 1.032-8.934, p=0.044).

Conclusions: The results of our study suggested the potential interest of GGH -401C>T as a predictive factor of the outcome of cervical carcinoma treated with cisplatin-based chemoradiotherapy.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chemoradiotherapy / methods
  • Cisplatin / administration & dosage*
  • Disease-Free Survival
  • Female
  • Humans
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Predictive Value of Tests
  • Radiation-Sensitizing Agents / administration & dosage*
  • Retrospective Studies
  • Survival Rate
  • Time Factors
  • Uterine Cervical Neoplasms / enzymology
  • Uterine Cervical Neoplasms / genetics*
  • Uterine Cervical Neoplasms / mortality*
  • Uterine Cervical Neoplasms / therapy*
  • gamma-Glutamyl Hydrolase / genetics*
  • gamma-Glutamyl Hydrolase / metabolism

Substances

  • Radiation-Sensitizing Agents
  • gamma-Glutamyl Hydrolase
  • Cisplatin