Published April 1, 2012 | Version v1
Journal article

Use of Germline Polymorphisms in Predicting Concurrent Chemoradiotherapy Response in Esophageal Cancer

  • 1. Department of Statistics and Informatics Science, Providence University, Taiwan (China)
  • 2. Department of Public Health, Institute of Epidemiology, National Taiwan University, Taiwan (China)
  • 3. Research Center for Gene, Environment, and Human Health, College of Public Health, National Taiwan University, Taiwan (China)
  • 4. Institute of Epidemiology Preventive Medicine, College of Public Health, National Taiwan University, Taiwan (China)
  • 5. Graduate Institute of Physiology, National Taiwan University, Taiwan (China)
  • 6. Institute of Biotechnology, National Taiwan University, Taiwan (China)
  • 7. National Clinical Trial and Research Center, National Taiwan University Hospital, Taiwan (China)
  • 8. Department of Surgery, National Taiwan University Hospital, Taiwan (China)
  • 9. Bioinformatics and Biostatistics Core, Research Center for Medical Excellence, National Taiwan University, Taiwan (China)
  • 10. Graduate Institute of Biomedical Electronics and Bioinformatics, National Taiwan University, Taiwan (China)

Description

Purpose: To identify germline polymorphisms to predict concurrent chemoradiation therapy (CCRT) response in esophageal cancer patients. Materials and Methods: A total of 139 esophageal cancer patients treated with CCRT (cisplatin-based chemotherapy combined with 40 Gy of irradiation) and subsequent esophagectomy were recruited at the National Taiwan University Hospital between 1997 and 2008. After excluding confounding factors (i.e., females and patients aged ≥70 years), 116 patients were enrolled to identify single nucleotide polymorphisms (SNPs) associated with specific CCRT responses. Genotyping arrays and mass spectrometry were used sequentially to determine germline polymorphisms from blood samples. These polymorphisms remain stable throughout disease progression, unlike somatic mutations from tumor tissues. Two-stage design and additive genetic models were adopted in this study. Results: From the 26 SNPs identified in the first stage, 2 SNPs were found to be significantly associated with CCRT response in the second stage. Single nucleotide polymorphism rs16863886, located between SGPP2 and FARSB on chromosome 2q36.1, was significantly associated with a 3.93-fold increase in pathologic complete response to CCRT (95% confidence interval 1.62–10.30) under additive models. Single nucleotide polymorphism rs4954256, located in ZRANB3 on chromosome 2q21.3, was associated with a 3.93-fold increase in pathologic complete response to CCRT (95% confidence interval 1.57–10.87). The predictive accuracy for CCRT response was 71.59% with these two SNPs combined. Conclusions: This is the first study to identify germline polymorphisms with a high accuracy for predicting CCRT response in the treatment of esophageal cancer.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2011.02.036

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2011.02.036;
PII
S0360-3016(11)00337-3;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
82
Journal Issue
5
Journal Page Range
p. 1996-2003
ISSN
0360-3016
CODEN
IOBPD3

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.