USE OF GERMLINE POLYMORPHISMS IN PREDICTING CONCURRENT CHEMORADIOTHERAPY RESPONSE IN ESOPHAGEAL CANCER

被引:15
作者
Chen, Pei-Chun [2 ]
Chen, Yen-Ching [3 ,4 ,5 ]
Lai, Liang-Chuan [6 ]
Tsai, Mong-Hsun [7 ]
Chen, Shin-Kuang [8 ]
Yang, Pei-Wen [9 ]
Lee, Yung-Chie [9 ]
Hsiao, Chuhsing K. [4 ,5 ,10 ]
Lee, Jang-Ming [9 ]
Chuang, Eric Y. [1 ,8 ,10 ]
机构
[1] Natl Taiwan Univ, Dept Elect Engn, Grad Inst Biomed Elect & Bioinformat, Taipei 106, Taiwan
[2] Providence Univ, Dept Stat & Informat Sci, Taichung, Taiwan
[3] Natl Taiwan Univ, Coll Publ Hlth, Inst Epidemiol Prevent Med, Taipei 106, Taiwan
[4] Natl Taiwan Univ, Coll Publ Hlth, Res Ctr Gene Environm & Human Hlth, Taipei 106, Taiwan
[5] Natl Taiwan Univ, Dept Publ Hlth, Inst Epidemiol, Taipei 106, Taiwan
[6] Natl Taiwan Univ, Grad Inst Physiol, Taipei 106, Taiwan
[7] Natl Taiwan Univ, Inst Biotechnol, Taipei 106, Taiwan
[8] Natl Taiwan Univ Hosp, Natl Clin Trial & Res Ctr, Taipei, Taiwan
[9] Natl Taiwan Univ Hosp, Dept Surg, Taipei, Taiwan
[10] Natl Taiwan Univ, Res Ctr Med Excellence, Taipei 106, Taiwan
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2012年 / 82卷 / 05期
关键词
Esophageal cancer; Chemoradiation; Response; Germline polymorphism; Biomarker; SQUAMOUS-CELL CARCINOMA; PREOPERATIVE CHEMORADIOTHERAPY; PATHOLOGICAL RESPONSE; NEOADJUVANT THERAPY; PROSTATE-CANCER; ASSOCIATION; SURGERY; RISK; SPHINGOSINE-1-PHOSPHATE; CHEMORADIATION;
D O I
10.1016/j.ijrobp.2011.02.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2012 Elsevier Inc.
引用
收藏
页码:1996 / 2003
页数:8
相关论文
共 34 条
[1]   GNAS1 T393C polymorphism is associated with histopathological response to neoadjuvant radiochemotherapy in esophageal cancer [J].
Alakus, H. ;
Warnecke-Eberz, U. ;
Bollschweiler, E. ;
Moenig, S. P. ;
Vallboehmer, D. ;
Brabender, J. ;
Drebber, U. ;
Baldus, S. E. ;
Riemann, K. ;
Siffert, W. ;
Hoelscher, A. H. ;
Metzger, R. .
PHARMACOGENOMICS JOURNAL, 2009, 9 (03) :202-207
[2]  
[Anonymous], 1996, ARCH SURG-CHICAGO, V131, P824, DOI DOI 10.1001/ARCH-SURG.1996.01430200029005
[3]   Chemoradiotherapy followed by surgery compared with surgery alone in squamous-cell cancer of the esophagus [J].
Bosset, JF ;
Gignoux, M ;
Triboulet, JP ;
Tiret, E ;
Mantion, G ;
Elias, D ;
Lozach, P ;
Ollier, JC ;
Pavy, JJ ;
Mercier, M ;
Sahmoud, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (03) :161-167
[4]   Sequence variants of toll-like receptor 4 and susceptibility to prostate cancer [J].
Chen, YC ;
Giovannucci, E ;
Lazarus, R ;
Kraft, P ;
Ketkar, S ;
Hunter, DJ .
CANCER RESEARCH, 2005, 65 (24) :11771-11778
[5]   Preoperative chemoradiotherapy for squamous cell carcinoma and adenocarcinoma of the esophagus - A phase II study [J].
De Vita, F ;
Di Martino, N ;
Orditura, M ;
Cosenza, A ;
Galizia, G ;
Del Genio, A ;
Catalano, G .
CHEST, 2002, 122 (04) :1302-1308
[6]   Preoperative chemoradiotherapy for oesophageal cancer:: a systematic review and meta-analysis [J].
Fiorica, F ;
Di Bona, D ;
Schepis, F ;
Licata, A ;
Shahied, L ;
Venturi, A ;
Falchi, AM ;
Craxí, A ;
Cammà, C .
GUT, 2004, 53 (07) :925-930
[7]   Identification of multiple distinct Snf2 subfamilies with conserved structural motifs [J].
Flaus, Andrew ;
Martin, David M. A. ;
Barton, Geoffrey J. ;
Owen-Hughes, Tom .
NUCLEIC ACIDS RESEARCH, 2006, 34 (10) :2887-2905
[8]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[9]   Genetic Variations in the PI3K/PTEN/AKT/mTOR Pathway Are Associated With Clinical Outcomes in Esophageal Cancer Patients Treated With Chemoradiotherapy [J].
Hildebrandt, Michelle A. T. ;
Yang, Hushan ;
Hung, Mien-Chie ;
Izzo, Julie G. ;
Huang, Maosheng ;
Lin, Jie ;
Ajani, Jaffer A. ;
Wu, Xifeng .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (06) :857-871
[10]   Treatment outcomes of resected esophageal cancer [J].
Hofstetter, W ;
Swisher, SG ;
Correa, AM ;
Hess, K ;
Putnam, JB ;
Ajani, JA ;
Dolormente, M ;
Francisco, R ;
Komaki, RR ;
Lara, A ;
Martin, F ;
Rice, DC ;
Sarabia, AJ ;
Smythe, WR ;
Vaporciyan, AA ;
Walsh, GL ;
Roth, JA .
ANNALS OF SURGERY, 2002, 236 (03) :376-385