Davey Matthew G, Jalali Amirhossein, Ryan Éanna J, McLaughlin Ray P, Sweeney Karl J, Barry Michael K, Malone Carmel M, Keane Maccon M, Lowery Aoife J, Miller Nicola, Kerin Michael J
The Lambe Institute for Translational Research, National University of Ireland, H91 TK33 Galway, Ireland.
Department of Surgery, Galway University Hospitals, H91 YR71 Galway, Ireland.
J Pers Med. 2022 Jul 8;12(7):1117. doi: 10.3390/jpm12071117.
Background: OncotypeDX Recurrence Score© (RS) is a commercially available 21-gene expression assay which estimates prognosis and guides chemoendocrine prescription in early-stage estrogen-receptor positive, human epidermal growth factor receptor-2-negative (ER+/HER2−) breast cancer. Limitations of RS testing include the cost and turnaround time of several weeks. Aim: Our aim is to develop a user-friendly surrogate nomogram capable of predicting RS. Methods: Multivariable linear regression analyses were performed to determine predictors of RS and RS > 25. Receiver operating characteristic analysis produced an area under the curve (AUC) for each model, with training and test sets were composed of 70.3% (n = 315) and 29.7% (n = 133). A dynamic, user-friendly nomogram was built to predict RS using R (version 4.0.3). Results: 448 consecutive patients who underwent RS testing were included (median age: 58 years). Using multivariable regression analyses, postmenopausal status (β-Coefficient: 0.25, 95% confidence intervals (CIs): 0.03−0.48, p = 0.028), grade 3 disease (β-Coefficient: 0.28, 95% CIs: 0.03−0.52, p = 0.026), and estrogen receptor (ER) score (β-Coefficient: −0.14, 95% CIs: −0.22−−0.06, p = 0.001) all independently predicted RS, with AUC of 0.719. Using multivariable regression analyses, grade 3 disease (odds ratio (OR): 5.67, 95% CIs: 1.32−40.00, p = 0.037), decreased ER score (OR: 1.33, 95% CIs: 1.02−1.66, p = 0.050) and decreased progesterone receptor score (OR: 1.16, 95% CIs: 1.06−1.25, p = 0.002) all independently predicted RS > 25, with AUC of 0.740 for the static and dynamic online nomogram model. Conclusions: This study designed and validated an online user-friendly nomogram from routinely available clinicopathological parameters capable of predicting outcomes of the 21-gene RS expression assay.
OncotypeDX复发评分(RS)是一种可商业化获得的21基因表达检测方法,用于评估早期雌激素受体阳性、人表皮生长因子受体2阴性(ER+/HER2−)乳腺癌的预后并指导化学内分泌治疗方案的制定。RS检测的局限性包括成本高以及周转时间长达数周。目的:我们的目的是开发一种用户友好的替代列线图,能够预测RS。方法:进行多变量线性回归分析以确定RS以及RS>25的预测因素。受试者工作特征分析得出每个模型的曲线下面积(AUC),训练集和测试集分别由70.3%(n = 315)和29.7%(n = 133)组成。使用R(版本4.0.3)构建了一个动态、用户友好的列线图来预测RS。结果:纳入了448例连续接受RS检测的患者(中位年龄:58岁)。通过多变量回归分析,绝经后状态(β系数:0.25,95%置信区间(CIs):0.03−0.48,p = 0.028)、3级疾病(β系数:0.28,95% CIs:0.03−0.52,p = 0.026)和雌激素受体(ER)评分(β系数:−0.14,95% CIs:−0.22−−0.06,p = 0.001)均独立预测RS,AUC为0.719。通过多变量回归分析,3级疾病(比值比(OR):5.67,95% CIs:1.32−40.00,p = 0.037)、ER评分降低(OR:1.33,95% CIs:1.02−1.66,p = 0.050)和孕激素受体评分降低(OR:1.16,95% CIs:1.06−1.25,p = 0.002)均独立预测RS>25,静态和动态在线列线图模型的AUC为0.740。结论:本研究从常规可用的临床病理参数设计并验证了一种在线用户友好的列线图,能够预测21基因RS表达检测的结果。