Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Yanjiang West Road 107#, Guangzhou, 510120, China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Department of Pathology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
BMC Cancer. 2019 Jun 6;19(1):541. doi: 10.1186/s12885-019-5703-4.
Triple negative breast cancer (TNBC) is an aggressive and heterogeneous disease. Nomograms predicting outcomes of TNBC are needed for risk management.
Nomograms were based on an analysis of 296 non-metastatic TNBC patients treated at Sun Yat-sen Memorial Hospital from 2002 to 2014. The end points were disease-free survival (DFS) and overall survival (OS). Predictive accuracy and discriminative ability were evaluated by concordance index (C-index), area under the curve (AUC) and calibration curve, and compared with the American Joint Committee on Cancer (AJCC) staging system, PREDICT and CancerMath. Models were subjected to bootstrap internal validation and external validation using independent cohorts of 191 patients from the second Xiangya Hospital and Peking University Shenzhen Hospital between 2007 and 2012.
On multivariable analysis of training cohort, independent prognostic factors were stromal tumor-infiltrating lymphocytes (TILs), tumor size, node status, and Ki67 index, which were then selected into the nomograms. The calibration curves for probability of DFS and OS showed optimal agreement between nomogram prediction and actual observation. The C-index of nomograms was significantly higher than that of the seventh and eighth AJCC staging system for predicting DFS (training: 0.743 vs 0.666 (P = 0.003) and 0.664 (P = 0.024); validation: 0.784 vs 0.632 (P = 0.02) and 0.607 (P = 0.002)) and OS (training: 0.791 vs 0.683 (P = 0.004) and 0.677 (P < 0.001); validation: 0.783 vs 0.656 (P = 0.006) and 0.606 (P = 0.001)). Our nomograms had larger AUCs compared with PREDICT and CancerMath. In addition, the nomograms showed good performance in stratifying different risk groups of patients both in the training and validation cohorts.
We have developed novel and practical nomograms that can provide individual prediction of DFS and OS for TNBC based on stromal TILs, tumor size, node status, and Ki67 index. Our nomograms may help clinicians in risk consulting and selection of long term survivors.
三阴性乳腺癌(TNBC)是一种侵袭性和异质性疾病。需要预测 TNBC 患者结局的列线图来进行风险管理。
列线图基于 2002 年至 2014 年在中山大学孙逸仙纪念医院治疗的 296 例非转移性 TNBC 患者的分析。终点为无病生存(DFS)和总生存(OS)。通过一致性指数(C 指数)、曲线下面积(AUC)和校准曲线评估预测准确性和判别能力,并与美国癌症联合委员会(AJCC)分期系统、PREDICT 和 CancerMath 进行比较。使用来自 2007 年至 2012 年第二湘雅医院和北京大学深圳医院的 191 例独立队列进行了模型的 bootstrap 内部验证和外部验证。
在训练队列的多变量分析中,独立的预后因素是基质肿瘤浸润淋巴细胞(TILs)、肿瘤大小、淋巴结状态和 Ki67 指数,这些因素被选入列线图。DFS 和 OS 的概率校准曲线显示列线图预测与实际观察之间具有最佳一致性。列线图的 C 指数显著高于第七和第八版 AJCC 分期系统预测 DFS(训练:0.743 与 0.666(P=0.003)和 0.664(P=0.024);验证:0.784 与 0.632(P=0.02)和 0.607(P=0.002))和 OS(训练:0.791 与 0.683(P=0.004)和 0.677(P<0.001);验证:0.783 与 0.656(P=0.006)和 0.606(P=0.001))。与 PREDICT 和 CancerMath 相比,我们的列线图具有更大的 AUC。此外,在训练和验证队列中,这些列线图在分层不同风险组的患者方面均表现出良好的性能。
我们开发了新的实用列线图,可以基于基质 TILs、肿瘤大小、淋巴结状态和 Ki67 指数为 TNBC 患者提供 DFS 和 OS 的个体预测。我们的列线图可能有助于临床医生进行风险咨询和选择长期生存者。