Montagna Emilia, Vingiani Andrea, Maisonneuve Patrick, Cancello Giuseppe, Contaldo Federica, Pruneri Giancarlo, Colleoni Marco
Division of Medical Senology, European Institute of Oncology, Via Ripamonti 435, 20141, Milan, Italy.
Biobank for Translational Medicine Unit, Department of Pathology, European Institute of Oncology, Via Ripamonti 435, 20141, Milan, Italy.
Breast. 2017 Aug;34:83-88. doi: 10.1016/j.breast.2017.05.009. Epub 2017 May 23.
High levels of tumor-infiltrating lymphocytes (TILs) in primary triple negative and HER2-positive breast cancer (BC) have been associated with an improved patients' outcome. The role of TILs in Luminal (hormone receptor positive and HER2 negative) tumors remains to be elucidated. Moreover, the association between TILs and prognosis in the metastatic setting is still unknown.
We evaluated the relationship between TILs and time to progression (TTP) in metastatic BC patients enrolled in a prospective phase II trial of metronomic chemotherapy, that used cyclophosphamide 50 mg daily, capecitabine 500 mg thrice daily and vinorelbine 40 mg orally three times a week (VEX combination).
Of the 108 ER + BC patients enrolled in the VEX trial, 92 (85%) had sufficient tumor tissue and were assessed for TILs in H&E stained slides. TILs were evaluated in 38 primary BC samples and 54 metastatic sites. High (≥10%) TILs levels were significantly correlated with high Ki-67 labeling index. At multivariable analysis, each 10% increase in TILs strongly predicted a worse TTP (HR: 1.27, p = 0.008). VEX trial patients, categorized by a 3 tiers system (0-4%, 5-9% and >10% TILs) showed significantly different progression free survival curves (p = 0.011).
High TILs levels are significantly associated with a worse TTP in Luminal metastatic BC patients treated by metronomic chemotherapy. Our data confirm the reliability of TILs as a biomarker in the BC metastatic setting. The putative unfavorable prognostic role of TILs in Luminal BC patients might have clinical utility if validated by further studies.
原发性三阴性和HER2阳性乳腺癌(BC)中高水平的肿瘤浸润淋巴细胞(TILs)与患者预后改善相关。TILs在管腔型(激素受体阳性且HER2阴性)肿瘤中的作用仍有待阐明。此外,TILs与转移性疾病预后之间的关联尚不清楚。
我们评估了参加节拍化疗前瞻性II期试验的转移性BC患者中TILs与疾病进展时间(TTP)的关系,该试验使用每日50 mg环磷酰胺、每日三次500 mg卡培他滨和每周三次口服40 mg长春瑞滨(VEX组合)。
在参加VEX试验的108例ER + BC患者中,92例(85%)有足够的肿瘤组织,并在苏木精和伊红(H&E)染色切片中评估TILs。在38个原发性BC样本和54个转移部位评估了TILs。高(≥10%)TILs水平与高Ki-67标记指数显著相关。在多变量分析中,TILs每增加10%强烈预示TTP更差(风险比:1.27,p = 0.008)。根据三级系统(0-4%、5-9%和>10% TILs)分类的VEX试验患者显示无进展生存曲线有显著差异(p = 0.011)。
在接受节拍化疗的管腔型转移性BC患者中,高TILs水平与更差的TTP显著相关。我们的数据证实了TILs作为BC转移环境中生物标志物的可靠性。如果通过进一步研究验证,TILs在管腔型BC患者中假定的不良预后作用可能具有临床实用性。