Pharoah P D, Guilford P, Caldas C
Department of Oncology, Strangeways Research Laboratories, University of Cambridge, Worts Causeway, Cambridge, CB18RN England, UK.
Gastroenterology. 2001 Dec;121(6):1348-53. doi: 10.1053/gast.2001.29611.
BACKGROUND & AIMS: Germline mutations in CDH1 are known to cause hereditary diffuse gastric cancer (HDGC). Breast and colorectal cancer have also been reported in CDH1-associated HDGC. The purpose of this study was to estimate the cumulative risk of gastric and breast cancer in CDH1 mutation carriers. METHODS: Family data were collected by member groups of the International Gastric Cancer Linkage Consortium. Eligible families had at least 3 cases of diffuse gastric cancer, and at least 1 affected member had tested positive for a mutation in CDH1. Eleven families met these criteria. We used the pedigree information to estimate penetrance using the MENDEL program. The conditional likelihood of the pedigree was maximized given the phenotype of the pedigree and genotype of the index case at ascertainment. We parameterized the model in terms of log relative risks for mutation carriers compared with risks in the general population of the United Kingdom. Noncarriers of the gene were assumed to develop the disease at population incidence rates. RESULTS: The estimated cumulative risk of gastric cancer by age 80 years was 67% for men (95% confidence interval [95% CI], 39-99) and 83% for women (95% CI, 58-99). For women, the cumulative risk of breast cancer was 39% (95% CI, 12-84). The combined risk of gastric cancer and breast cancer in women was 90% by age 80 years. CONCLUSIONS: These penetrance estimates should be useful for genetic counseling in multiple-case families. However, they may not apply to individuals with a minimal family history, in whom the risks may be lower.
背景与目的:已知CDH1基因的种系突变会导致遗传性弥漫性胃癌(HDGC)。CDH1相关的HDGC中也有乳腺癌和结直肠癌的报道。本研究的目的是估计CDH1突变携带者患胃癌和乳腺癌的累积风险。 方法:国际胃癌连锁联盟的成员小组收集了家族数据。符合条件的家族至少有3例弥漫性胃癌病例,且至少有1名受影响成员的CDH1突变检测呈阳性。11个家族符合这些标准。我们使用系谱信息,通过MENDEL程序估计外显率。在确定系谱的表型和索引病例的基因型的情况下,使系谱的条件似然性最大化。我们根据与英国普通人群风险相比的突变携带者的对数相对风险对模型进行参数化。假设基因的非携带者以人群发病率患该疾病。 结果:80岁时男性患胃癌的估计累积风险为67%(95%置信区间[95%CI],39 - 99),女性为83%(95%CI,58 - 99)。女性患乳腺癌的累积风险为39%(95%CI,12 - 84)。80岁时女性患胃癌和乳腺癌的综合风险为90%。 结论:这些外显率估计值对多病例家族的遗传咨询应是有用的。然而,它们可能不适用于家族史最少的个体,这些个体的风险可能较低。
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