Grigoriadis Anita, Gazinska Patrycja, Pai Trupti, Irhsad Sheeba, Wu Yin, Millis Rosemary, Naidoo Kalnisha, Owen Julie, Gillett Cheryl E, Tutt Andrew, Coolen Anthonius Cc, Pinder Sarah E
Breast Cancer Now Research Unit, Innovation Hub, Cancer Centre at Guy's Hospital, Faculty of Life Sciences and Medicine, King's College LondonLondonUK.
School of Cancer and Pharmaceutical SciencesCRUK King's Health Partners Centre, King's College London, Innovation Hub, Cancer Centre at Guy's Hospital, Great Maze PondLondonUK.
J Pathol Clin Res. 2018 Jan 8;4(1):39-54. doi: 10.1002/cjp2.87. eCollection 2018 Jan.
The prognostic importance of lymph node (LN) status and tumour-infiltrating lymphocytes (TILs), is well established, particularly TILs in triple negative breast cancers (TNBCs). So far, few studies have interrogated changes in involved and uninvolved LNs and evaluated if their morphological patterns add valuable information for the prediction of disease progression in breast cancer. In a cohort of 309 patients enriched for TNBCs (170/309), we histologically characterised immune and stromal features in primary tumours and associated involved and uninvolved axillary LNs on routine haematoxylin and eosin stained sections. Of the 309 patients, 143 had LN-positive disease. Twenty-five histopathological features were assessed, including the degree of TIL presence, quantitative and qualitative assessment of germinal centres (GCs) and sinus histiocytosis. Multivariate and cross-validated proportional hazard regression analyses were used to identify optimal covariate sets for prediction of distant metastasis-free survival (DMFS). The degree of intratumoural and peritumoural immune infiltrate was associated with architectural changes in both uninvolved and involved LNs. By including clinicopathological characteristics as well as tumour and LN histopathological features in L2-regularised proportional hazard models, the prediction of 5-year DMFS was improved by 3-15% over the baseline in all cancers and in TNBCs. In LN-positive cancers, the combination of Salgado's classification, lymphocytic lobulitis, size and number of GCs in the uninvolved LNs and location of GCs in the involved LNs carried significant prognostic information. From these features, a multivariate cross-validation-stable risk signature was constructed, which identified low-risk groups within both LN-positive breast cancers and the LN-positive TNBCs group with a 10-year DMFS probability of 78 and 87%, respectively. This study illustrates that, by incorporating histopathological patterns of involved and uninvolved LNs combined with primary tumour immune and stromal features, the prediction of developing distant metastasis in LN-positive breast cancers can be estimated more accurately.
淋巴结(LN)状态和肿瘤浸润淋巴细胞(TILs)的预后重要性已得到充分证实,尤其是三阴性乳腺癌(TNBCs)中的TILs。到目前为止,很少有研究探讨受累和未受累淋巴结的变化,并评估其形态学模式是否为乳腺癌疾病进展的预测增加有价值的信息。在一组309例以TNBCs为主的患者队列(170/309)中,我们在常规苏木精和伊红染色切片上对原发性肿瘤以及相关的受累和未受累腋窝淋巴结的免疫和基质特征进行了组织学表征。309例患者中,143例有淋巴结阳性疾病。评估了25种组织病理学特征,包括TIL存在程度、生发中心(GCs)的定量和定性评估以及窦组织细胞增生。使用多变量和交叉验证的比例风险回归分析来确定预测无远处转移生存期(DMFS) 的最佳协变量集。肿瘤内和肿瘤周围免疫浸润程度与未受累和受累淋巴结的结构变化相关。通过将临床病理特征以及肿瘤和淋巴结组织病理学特征纳入L2正则化比例风险模型,所有癌症和TNBCs的5年DMFS预测较基线提高了3%-15%。在淋巴结阳性癌症中,Salgado分类、淋巴细胞性小叶炎、未受累淋巴结中GCs的大小和数量以及受累淋巴结中GCs的位置的组合具有显著的预后信息。根据这些特征,构建了一个多变量交叉验证稳定风险特征,该特征在淋巴结阳性乳腺癌和淋巴结阳性TNBCs组中分别识别出10年DMFS概率为78%和87%的低风险组。这项研究表明,通过纳入受累和未受累淋巴结的组织病理学模式以及原发性肿瘤免疫和基质特征,可以更准确地估计淋巴结阳性乳腺癌发生远处转移的可能性。