Tsai Michaela L, Lillemoe Tamera J, Finkelstein Marsha J, Money Joel E, Susnik Barbara, Grimm Erin, Kang Sung-Hae L, Swenson Karen K
Allina Health System, Virginia Piper Cancer Institute, Minneapolis, MN.
Hospital Pathology Associates and Allina Health Laboratories, Minneapolis, MN.
Clin Breast Cancer. 2016 Feb;16(1):45-50. doi: 10.1016/j.clbc.2015.08.001. Epub 2015 Aug 19.
INTRODUCTION/BACKGROUND: Oncotype DX (Genomic Health, Redwood City, CA) uses reverse transcriptase polymerase chain reaction analysis to measure tumor gene expression for determining recurrence risk (RR) and guiding chemotherapy decisions for breast cancer patients. Invasive lobular carcinoma (ILC) is a histologic subtype that has not been the focus of prior studies validating Oncotype DX. The study purpose was to develop a model using histologic tumor characteristics to predict uniformly low Oncotype DX Recurrence Scores (RS) in ILC.
ILC cases in our pathology database with Oncotype DX testing were identified. Histologic tumor characteristics, immunohistochemical (IHC) of estrogen receptor (ER)/progesterone receptor (PgR) percent, HER2, E-cadherin expression, and Ki-67 levels were obtained for cases. Discriminant analysis was used to test the hypothesis that tumors classified as lower/higher risk based on Oncotype DX RS would differ significantly on a linear combination of variables.
From 2006 - 2014, 158 cases of ILC having Oncotype DX testing were identified; 90 low risk (RS < 18), 66 intermediate risk (RS 18 - 30) and 2 high risk (RS > 30). Discriminant analysis showed that PgR% followed by Ki-67 provided the greatest contribution to discern low versus elevated RS. A subset of 57 cases (∼36%) with predicted probabilities > 86% for either low or high RS yielded 96.5% correct classification, 92.3% sensitivity, and 97.7% specificity.
Our analytical model may be useful in predicting lower RR in patients with ILC. If validated, this provides a faster and less expensive alternative to Oncotype DX testing in certain patients with ILC.
引言/背景:Oncotype DX(基因健康公司,加利福尼亚州红木城)采用逆转录聚合酶链反应分析来测量肿瘤基因表达,以确定复发风险(RR)并指导乳腺癌患者的化疗决策。浸润性小叶癌(ILC)是一种组织学亚型,此前尚未成为验证Oncotype DX的研究重点。本研究目的是开发一种利用肿瘤组织学特征预测ILC中Oncotype DX复发评分(RS)均一性较低的模型。
在我们的病理数据库中识别出接受Oncotype DX检测的ILC病例。获取病例的肿瘤组织学特征、雌激素受体(ER)/孕激素受体(PgR)百分比的免疫组织化学(IHC)、HER2、E-钙黏蛋白表达以及Ki-67水平。采用判别分析来检验基于Oncotype DX RS分类为低/高风险的肿瘤在变量线性组合上是否存在显著差异的假设。
2006年至2014年,共识别出158例接受Oncotype DX检测的ILC病例;90例低风险(RS < 18),66例中风险(RS 18 - 30),2例高风险(RS > 30)。判别分析显示,PgR%其次是Ki-67对区分低RS与高RS的贡献最大。57例(约36%)低或高RS预测概率> 86%的病例子集,分类正确率为96.5%,敏感性为92.3%,特异性为97.7%。
我们的分析模型可能有助于预测ILC患者较低的RR。如果得到验证,这为某些ILC患者提供了一种比Oncotype DX检测更快且成本更低的替代方法。