Department of Clinical Cancer Prevention, University of Texas MD Anderson Cancer Center, Houston, 77230, USA.
Cancer Prev Res (Phila). 2011 Oct;4(10):1609-16. doi: 10.1158/1940-6207.CAPR-10-0361. Epub 2011 Jul 27.
Screening mammography results in the increased detection of indolent tumors. We hypothesized that screen- and symptom-detected tumors would show genotypic differences as copy number imbalances (CNI) that, in part, explain differences in the clinical behavior between screen- and symptom-detected breast tumors. We evaluated 850 women aged 40 and above diagnosed with stage I and II breast cancer at the University of Texas MD Anderson Cancer Center between 1985 and 2000 with information available on method of tumor detection (screen vs. symptoms). CNIs in screen- and symptom-detected tumors were identified using high-density molecular inversion probe arrays. Cox proportional modeling was used to estimate the effect of method of tumor detection on disease-free survival after adjusting for age, stage, and the CNIs. The majority of tumors were symptom detected (n = 603) compared with screen detected (n = 247). Copy number gains in chromosomes 2p, 3q, 8q, 11p, and 20q were associated with method of breast cancer detection (P < 0.00001). We estimated that 32% and 63% of the survival advantage of screen detection was accounted for by age, stage, nuclear grade, and Ki67 in women aged 50 to 70 and aged 40 to 87, respectively. In each age category, an additional 20% of the survival advantage was accounted for by CNIs associated with method of detection. Specific CNIs differ between screen- and symptom-detected tumors and explain part of the survival advantage associated with screen-detected tumors. Measurement of tumor genotype has the potential to improve discrimination between indolent and aggressive screen-detected tumors and aids patient and physician decision making about use of surgical and adjuvant treatments.
乳腺 X 线筛查可提高惰性肿瘤的检出率。我们假设,筛查检出和症状检出的肿瘤会表现出基因差异,部分原因是解释了两者在临床行为上的差异。我们评估了 1985 年至 2000 年间在德克萨斯大学 MD 安德森癌症中心诊断为 I 期和 II 期乳腺癌的 850 名年龄在 40 岁及以上的女性,这些患者的肿瘤检测方法(筛查或症状)信息可用。使用高密度分子反转探针阵列来确定筛查和症状检出肿瘤中的拷贝数失衡(CNI)。使用 Cox 比例风险模型,在调整年龄、分期和 CNI 后,估计肿瘤检测方法对无病生存的影响。与筛查检出的肿瘤(n=247)相比,大多数肿瘤为症状检出(n=603)。染色体 2p、3q、8q、11p 和 20q 的拷贝数增益与乳腺癌检测方法相关(P<0.00001)。我们估计,50-70 岁和 40-87 岁女性中,筛查检出的生存优势的 32%和 63%分别由年龄、分期、核分级和 Ki67 解释。在每个年龄组中,与检测方法相关的 CNI 又解释了 20%的生存优势。筛查检出和症状检出肿瘤之间存在特定的 CNI 差异,这些差异部分解释了筛查检出肿瘤的生存优势。肿瘤基因型的测量有可能改善对惰性和侵袭性筛查检出肿瘤的区分,并有助于患者和医生在手术和辅助治疗的使用方面做出决策。