GENETIC PREDISPOSITION TESTING IN COLORECTAL CANCER

基因技术的爆炸式发展使识别癌症风险增加的个体成为可能，并为癌症筛查和预防工作创造了可能性。然而，遗传易感性检测实际上是一种有效和具有成本效益的临床策略的情况是不确定的。 最近描述的APC基因密码子I1307 K中的低突变率种系突变似乎增加了德系犹太人患结直肠癌的风险，这强调了批判性地评估何时以及如何将基因检测策略纳入临床癌症预防的必要性。 我们提出了一个遗传流行病学研究德系犹太人结直肠癌和息肉，评估I1307 K APC突变的意义。 我们的研究结果将用于构建一个决策分析模型，该模型提供了一个全面的框架，用于预测该基因以及其他结肠癌易感基因的预测性检测的临床重要性和政策影响。 实现这些目标的具体目标是：1.确定遗传性I1307 K APC突变在美国和以色列德系犹太人结直肠癌或腺瘤性息肉的医院队列中的意义。通过评估基因频率和突变率，该分析将评估遗传性I1307 K APC突变增加癌症风险的程度以及突变相关肿瘤是否具有特定的预后特征。 2. 评估遗传性结直肠癌易感性基因检测的有效性（以生命年和质量调整生命年衡量）和成本效益。 特别是，我们将研究基因频率，基因频率，年龄，家族史，测试特征，相关成本和知识驱动的筛选依从性对基因检测策略的成本效益的影响。达纳-法伯癌症研究所人口科学部的教师赞助商将为候选人提供实现这些目标的关键指导，并作为一名专注于评估遗传技术在癌症预防中的应用的研究人员获得独立性。

The explosion of genetic technology makes identification of individuals with increased cancer risks possible and creates the potential to target cancer screening and prevention efforts. However, the circumstances where genetic predisposition testing is actually an effective and cost-effective clinical strategy are uncertain. A recently described low-penetrance germline mutation in codon I1307K of the APC gene that appears to increase colorectal cancer risk among Ashkenazi Jews underscores the need to critically evaluate when and how genetic testing strategies should be incorporated into clinical cancer prevention. We propose a genetic epidemiologic study among Ashkenazi patients with colorectal cancer and polyps that evaluates the significance of I1307K APC mutations. Our findings will be used to construct a decision analysis model that provides a comprehensive framework for predicting the clinical importance and policy implications of predictive testing for this as well as for other colon cancer predisposing genes. The specific aims to accomplish these goals are: 1. To determine the significance of inherited I1307K APC mutations in a hospital-based cohort of American and Israeli Ashkenazi Jews with colorectal cancer or adenomatous polyps. By evaluating gene frequency and penetrance, this analysis will assess the extent to which inherited I1307K APC mutations increase cancer risk and whether mutation-associated tumors have particular prognostic features. 2. To assess the effectiveness, measured in life-years and quality-adjusted life years, and the cost-effectiveness, of genetic testing for inherited colorectal cancer susceptibility. In particular, we will examine the impact of gene penetrance, gene frequency, age, family history, test characteristics, associated costs, and knowledge motivated screening compliance on the cost-effectiveness of genetic testing strategies. Faculty sponsors in the Division of Population Sciences at the Dana-Farber Cancer Institute will provide the candidate with the guidance critical to accomplishing these aims and to attaining independence as an investigator focused on evaluating the application of genetic technologies to cancer prevention.