Casablanca Yovanni, Wang Guisong, Lankes Heather A, Tian Chunqiao, Bateman Nicholas W, Miller Caela R, Chappell Nicole P, Havrilesky Laura J, Wallace Amy Hooks, Ramirez Nilsa C, Miller David S, Oliver Julie, Mitchell Dave, Litzi Tracy, Blanton Brian E, Lowery William J, Risinger John I, Hamilton Chad A, Phippen Neil T, Conrads Thomas P, Mutch David, Moxley Katherine, Lee Roger B, Backes Floor, Birrer Michael J, Darcy Kathleen M, Maxwell George Larry
Gynecologic Cancer Center of Excellence, Department of Gynecologic Surgery and Obstetrics, Uniformed Services University of the Health Sciences, Walter Reed National Military Medical Center, Bethesda, MD 20889, USA.
The Henry M Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD 20817, USA.
Cancers (Basel). 2022 Aug 23;14(17):4070. doi: 10.3390/cancers14174070.
A risk assessment model for metastasis in endometrioid endometrial cancer (EEC) was developed using molecular and clinical features, and prognostic association was examined. Patients had stage I, IIIC, or IV EEC with tumor-derived RNA-sequencing or microarray-based data. Metastasis-associated transcripts and platform-centric diagnostic algorithms were selected and evaluated using regression modeling and receiver operating characteristic curves. Seven metastasis-associated transcripts were selected from analysis in the training cohorts using 10-fold cross validation and incorporated into an MS7 classifier using platform-specific coefficients. The predictive accuracy of the MS7 classifier in Training-1 was superior to that of other clinical and molecular features, with an area under the curve (95% confidence interval) of 0.89 (0.80-0.98) for MS7 compared with 0.69 (0.59-0.80) and 0.71 (0.58-0.83) for the top evaluated clinical and molecular features, respectively. The performance of MS7 was independently validated in 245 patients using RNA sequencing and in 81 patients using microarray-based data. MS7 + MI (myometrial invasion) was preferrable to individual features and exhibited 100% sensitivity and negative predictive value. The MS7 classifier was associated with lower progression-free and overall survival ( ≤ 0.003). A risk assessment classifier for metastasis and prognosis in EEC patients with primary tumor derived MS7 + MI is available for further development and optimization as a companion clinical support tool.
利用分子和临床特征建立了子宫内膜样子宫内膜癌(EEC)转移风险评估模型,并对其预后相关性进行了研究。患者患有I期、IIIC期或IV期EEC,伴有肿瘤来源的RNA测序或基于微阵列的数据。使用回归建模和受试者工作特征曲线选择并评估转移相关转录本和以平台为中心的诊断算法。在训练队列分析中,通过10倍交叉验证从分析中选择了7个转移相关转录本,并使用特定于平台的系数将其纳入MS7分类器。MS7分类器在Training-1中的预测准确性优于其他临床和分子特征,MS7的曲线下面积(95%置信区间)为0.89(0.80-0.98),而评估最高的临床和分子特征的曲线下面积分别为0.69(0.59-0.80)和0.71(0.58-0.83)。MS7的性能在245例使用RNA测序的患者和81例使用基于微阵列数据的患者中得到独立验证。MS7+肌层浸润(MI)优于个体特征,表现出100%的敏感性和阴性预测值。MS7分类器与较低的无进展生存期和总生存期相关(≤0.003)。对于原发性肿瘤为MS7+MI的EEC患者,可获得转移和预后风险评估分类器,作为临床辅助支持工具进一步开发和优化。