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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Cancer Prev Res (Phila). Author manuscript; available in PMC 2010 July 1.
Published in final edited form as:
PMCID: PMC2733247
NIHMSID: NIHMS120638

Emerging Molecular Technologies for Identifying the Risk of Second Cancers

Susan T. Mayne, Ph.D.1 and Stephen B. Gruber, M.D., Ph.D.2

Cancer is becoming an increasingly survivable disease, and the number of cancer survivors is increasing each year. Second or higher-order cancers now account for about 16% of incident cancers in the Surveillance, Epidemiology, and End Results (SEER) database (1). An important current research need is to understand which patients are at greatest risk for second cancers and thus the greatest potential beneficiaries of available or experimental targeted surveillance and chemoprevention strategies.

Research over the past decade has emphasized the development of cancer risk models based on host characteristics (e.g., age, sex, reproductive factors), exogenous exposures (e.g., human papillomavirus [HPV], environmental tobacco smoke) lifestyle factors (e.g., smoking, alcohol) and (for second cancers) tumor characteristics (e.g., disease site, stage). These models have moved the field of cancer risk prediction forward in regard to both first and second cancers. In this issue of the journal, the field moves forward again with the report of Wu et al. (2), which examines a large number of gene polymorphisms in relation to the risk of second primary tumors/local recurrence in patients who have been curatively treated for early- stage squamous cell carcinomas of the oral cavity, pharynx, and larynx, the first large-scale evaluation of this type in head and neck cancer patients. The results are striking. The authors offer data supporting the hypothesis that risk prediction significantly and substantially improves following the incorporation of genetic data (multiple risk loci) into prediction models and that second cancers are partially attributable to polygenic variation, as has been clearly demonstrated for first primary head and neck cancers (3).

Squamous cell carcinoma of the head and neck has been a model disease site for research in second primary prevention for several reasons. Patients with early-stage disease frequently are treated curatively, surviving their disease to be at risk for second cancers. The annual risk for second primary cancers is 5% among stage I/II patients (4). Second cancers and local recurrences are a major cause of morbidity and mortality in this patient population (4). Various chemopreventive approaches to reduce this risk of second cancers have met with disappointing results. Retinoids, beta-carotene, alpha-tocopherol, and N-acetylcysteine have been evaluated (5) in large-scale cancer prevention trials. Although chemoprevention trials in head and neck cancer have not been efficacious, these same trials are now contributing importantly to the understanding of the etiology of second head and neck cancer as investigators, such as Wu et al. (2), begin to mine the data from prospectively followed and carefully characterized patient populations.

The sample of patients in the Wu et al. analysis had histologically confirmed stage I or II head and neck squamous cell carcinoma and participated in the Retinoid Head and Neck Second Primary Trial, a randomized, placebo-controlled chemoprevention trial of daily low-dose 13-cis-retinoic acid in preventing second primary tumors over several years (6). The trial was well-designed and conducted but disproved the hypothesis that this particular retinoid could prevent second primary tumors overall-- the hazard ratio for second primary tumors in the 13-cis-retinoic acid versus placebo group was 1.06 (95% confidence interval = 0.83–1.35). Wu et al. (2) used a nested case-control approach in comparing single nucleotide polymorphisms (SNPs) in DNA from 150 patients who developed second primary tumors and local recurrences with SNPs from 300 patients who remained free of second primary tumors and local recurrences throughout the follow-up period. This ability to convert a null chemoprevention trial into an informative cohort study is an often unrecognized value of well-conducted chemoprevention trials —an important value considering how many trials have had disappointing findings in their primary efficacy analyses.

Wu et al. (2) did not use the increasingly popular genome-wide association (GWAS) approach to identify target variants of interest, using instead a candidate gene approach, where they examined a large number of genes thought to be related to carcinogenesis. They selected haplotype-tagging SNPs, SNPs in coding and regulatory regions, and functional SNPs based on allele frequency and other factors, leading to the inclusion of 8370 chromosomal and mitochondrial SNPs in nearly 1000 cancer-related genes for analysis. Less than half of the cases with second primary cancer or recurrence had DNA available for analysis, so the investigators wisely chose to focus on candidate genes because of the limited sample size. They then explored how these SNPs predict future disease status, using a variety of statistical approaches.

First, they examined the associations between SNPs with outcome (adjusted for multiple comparisons), identifying 6 chromosomal and 7 mitochondrial SNPs of interest. They tested each SNP under recessive, dominant, and additive models. It could be argued that the authors’ choice to evaluate each model increased the chances of false discovery since many investigators choose to rely on a single genetic model that provides a parsimonious statistical test when the underlying mode of inheritance is unknown (7, 8). However, the authors went further to diminish the impact of multiple comparisons.

For example, they examined the consistency of these associations via a bootstrap resampling procedure (100 times), finding that 12 chromosomal SNPs and 3 mitochondrial SNPs had a bootstrap p value < 0.01 80% of the time. Two of the 3 mitochondrial SNPS were in high linkage disequilibrium with the third and so were excluded from further analyses, leaving 13 SNPs having the most consistent associations with a poor outcome. The authors then examined the effect of carrying more vs. fewer unfavorable gentoypes by summing the number of unfavorable genotypes in the 13 selected SNPs. Carrying more of these unfavorable genotypes versus fewer was strongly predictive of outcome: persons with 8 or more unfavorable genotypes were at 27-fold increased risk of second primary cancer or recurrence compared to those with 4 or fewer unfavorable genotypes. Comparing receiver operator characteristic (ROC) curves that included the genotype data with ROC curves that only included known clinical and smoking variables revealed that adding genotype data significantly improved the sensitivity and specificity of outcome prediction (as measured by area under the curve [AUC]), with the AUC increasing from 0.64 (clinical plus smoking variables) to 0.81 (clinical, smoking, and genetic variables).

Another sophisticated statistical approach of Wu et al. in examining multi-level interactions of the various genotypes was a survival-tree analysis (using only chromosomal SNPs, apparently). The tree and final risk nodes (Supplementary Figure 1) are based on quite small sample sizes, so the order of selected SNPs and the SNP profiles that drive each node must be interpreted with caution. It becomes immediately evident upon examination of the tree, however, that second cancer risk is determined by the complex interplay of numerous genetic polymorphisms and that the risk conferred by a particular risk polymorphism can be readily offset by other genetic polymorphisms, suggesting that simple models of genetic risk (for low-frequency allelic variants) likely are not forthcoming.

Replication of findings as important and provocative as the present results of Wu et al. (2) is essential, albeit difficult to accomplish in this circumstance. The International Head and Neck Cancer Epidemiology Consortium (INHANCE) is an international consortium to support research in head and neck cancer epidemiology (www.inhance.iarc.fr). However, this consortium emphasizes first primary cancers. There are few, if any, existing resources in the world that have the same high-quality clinical data from a cohort of head-and-neck cancer patients, and none that we are aware of with longer follow-up. New technologies, however, may provide a window into even more data from studies like the Retinoid Head and Neck Second Primary Trial (6). Now that a list of candidate genes has been proposed, it may be possible to extract DNA from archived paraffin-embedded tissue from both cases and controls, all of whom are first primary cancer patients, to independently validate the Wu et al. findings. The quality and quantity of DNA from paraffin is usually insufficient to permit high-throughput genotyping of nearly 9,000 SNPs. Yet, the DNA derived from paraffin-samples is sufficient to genotype the 13 SNPs identified by Wu et al. (2) in very large, independent series of cases. Paraffin-derived DNA should permit these investigators to conduct a validation study among the 204 second primary and recurrent cases with retrievable blocks who could not be evaluated in the present study because of a lack of lymphocytes, as well as permitting validation studies by other research teams with large collections of archived tissue accompanied by good follow-up data.

The finding that incorporating data on selected genetic polymorphisms with more-standard (lifestyle, host) factors can substantially improve the prediction of cancer risk has not been consistently observed in the broader cancer literature. For example, Zheng et al. (9) found that adding information on 5 SNPs into risk models for prostate cancer increased the AUC under the ROC curve from 0.624 to only 0.633 (a statistically significant but relatively minor improvement), versus a model based on age, geographic region, and family history of prostate cancer. Similarly, Gail et al. (10) found that adding 7 SNPs identified in recent GWAS studies to the NCI’s Breast Cancer Risk Assessment Tool (which includes age at first live birth, age at menarche, number of first degree relatives with breast cancer, and number of previous benign breast biopsy examinations) improved the AUC for the NCI risk-assessment model from 0.607 to 0.632, also a relatively small change. Spitz et al. used a slightly different approach, developing a risk model for lung cancer (11) based on traditional risk factor data (environmental tobacco smoke, family history of cancer, dust exposure, prior respiratory disease, and smoking history variables) and then expanding the model with two markers of DNA repair capacity (mutagen sensitivity, host-cell reactivation; ref. 12). Incorporating the biomarker data significantly increased the AUCs, although the change was relatively modest (from 0.67 to 0.70 for former smokers and from 0.68 to 0.73 for current smokers). A critical difference between these studies and that of Wu et al. (2) is that these other studies included family history data. That is, incorporation of family history data in risk models may lessen the value of adding genotypic/phenotypic biomarker data to them, a hypothesis that can be readily tested in populations with available family history and genotypic data.

A critical question that was not answered by the analysis of Wu et al. (2) is whether they could identify genetic subgroups that may benefit most from the chemopreventive intervention (13-cis-retinoic acid) tested in their source trial. The authors commented on a preliminary finding that one variant in the MK167 (cell-cycle) gene was associated with retinoid efficacy; that is, it was both prognostic and predictive of treatment response, suggesting the possibility of personalized chemoprevention. This preliminary finding, as with all subgroup findings, must be interpreted with caution. However, there are other completed retinoid-based chemoprevention trials in head and neck cancer (13, 14) that could attempt to replicate this pharmacogenomic finding, assuming they have available DNA and with the caveat that they evaluated 3 different retinoids.

This report of Wu et al. has many implications. First, it highlights the value of collecting biospecimens along with lifestyle and demographic data in chemoprevention trials, whether primary prevention trials or trials aimed at second cancer prevention (see ref. 1). Second, it suggests that individualized data on allelic variation in common genes can significantly improve risk prediction, especially when family history is not already accounted for in the risk model. Third, it opens a window for other head-and-neck cancer studies to replicate its prognostic associations involving a very limited panel of SNPs. It also may be possible for other completed studies to try to replicate the pharmacogenomic finding involving one SNP, although these studies may lack statistical power to accomplish this. Last, it highlights the substantial progress that can be made by a capable team of multidisciplinary investigators using new technologies to ask timely questions. Molecular epidemiology has had its challenges (15), but Wu et al. (2) have shown that this field continues to provide new insights, including a clearer understanding of disease etiology along with enhanced possibilities for individualized risk prediction.

Acknowledgments

Grant support: Supported in part by Grant No. P50 CA97248 from the National Institutes of Health through the University of Michigan’s Head and Neck Specialized Program of Research Excellence.

Footnotes

Disclosure of Potential Conflicts of Interest

The authors disclosed that they have no potential conflicts of interest.

References

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