Polymorphisms of Vitamin D Receptor and Survival in Early-Stage Non–Small Cell Lung Cancer Patients
- Wei Zhou1,
- Rebecca S. Heist1,5,
- Geoffrey Liu1,5,
- Donna S. Neuberg2,6,
- Kofi Asomaning1,
- Li Su1,
- John C. Wain7,
- Thomas J. Lynch5,
- Edward Giovannucci3,4,8 and
- David C. Christiani1,4,5
- Departments of 1Environmental Health, 2Biostatistics, 3Nutrition, and 4Epidemiology, Harvard School of Public Health; 5Department of Medicine, Massachusetts General Hospital, 6Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 7Thoracic Surgery Unit, Department of Surgery, Massachusetts General Hospital, and 8Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts
- Requests for reprints:
Wei Zhou, Occupational Health Program, Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02115. Phone: 617-432-1641. Fax: 617-432-6981. E-mail: wzhou{at}hsph.harvard.edu
Abstract
Our previous analysis suggested that surgery season in the summer time and high vitamin D intake are associated with improved survival in early-stage non–small cell lung cancer (NSCLC) patients. Here, we investigated the associations of vitamin D receptor (VDR) polymorphisms of Cdx-2 G>A, FokI C>T, and BsmI C>T with overall survival (OS) and recurrence-free survival (RFS) in 373 early-stage NSCLC patients. The data were analyzed using log-rank test and Cox proportional hazards models. The median follow-up time was 71 months (range, 0.1-140 months), with 186 deaths and 127 recurrences. There was no association between VDR polymorphisms and survival, overall or among adenocarcinoma patients. Among squamous cell carcinoma (SCC) patients, the G/A+A/A genotype group of the Cdx-2 polymorphism was associated with better OS: the 5-year OS rates were 41% [95% confidence interval (95% CI), 28-53] for the G/G and 55% (95% CI, 39-71) for the G/A+A/A genotypes, respectively (P = 0.04, log-rank test), with the adjusted hazard ratio of 0.56 (95% CI, 0.33-0.95) for G/A+A/A versus G/G. For the joint effects of the three polymorphisms, subjects with two or more “protective” alleles have better OS among SCC patients, with the adjusted hazard ratios of 0.20 (95% CI, 0.09-0.48), 0.40 (95% CI, 0.19-0.87), and 0.43 (95% CI, 0.19-0.97), respectively, for subjects with two, three, and four or more “protective” alleles when compared with subjects with zero or one “protective” allele (Ptrend = 0.71). Similar associations were found in haplotype analysis and for RFS among SCC patients. In conclusion, VDR polymorphisms may be associated with improved survival among SCC patients of early-stage NSCLC. (Cancer Epidemiol Biomarkers Prev 2006;15(11):2239–45)
Footnotes
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Grant support: NIH grants CA092824, CA074386, CA090578, ES/CA 06409, CA119650-01A1, and ES00002; American Institute for Cancer Research; Flight Attendants Medical Research Institute Young Clinical Scientist Award; American Cancer Society Postdoctoral Fellowship; and Doris Duke Charaticable Foundation and Sue's Fund.
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- Accepted August 18, 2006.
- Received January 12, 2006.
- Revision received August 9, 2006.










