Park In Hae, Kong Sun-Young, Ro Jae Yoon, Kwon Youngmee, Kang Joo Hyun, Mo Hye Jin, Jung So-Youn, Lee Seeyoun, Lee Keun Seok, Kang Han-Sung, Lee Eunsook, Joo Jungnam, Ro Jungsil
Center for Breast Cancer, National Cancer Center, Goyang-si, Korea; Breast and Endocrine Center Branch of Research Institute, National Cancer Center, Goyang-si, Korea.
Translational Epidemiology Branch, Division of Cancer Epidemiology and Prevention, Research Institute, National Cancer Center, Goyang-si, Korea; Department of Laboratory Medicine, Center for Diagnostic Oncology, Hospital and Research Institute, National Cancer Center, Goyang-si, Korea.
Clin Breast Cancer. 2016 Feb;16(1):51-8. doi: 10.1016/j.clbc.2015.07.006. Epub 2015 Aug 6.
The immune system might influence breast cancer (BC) prognosis. However, the relationship between programmed death ligand 1 (PD-L1) and tumor-infiltrating lymphocyte (TIL) profiles remains unclear with respect to BC subtypes.
We investigated the relationship between TIL profiles for CD8+ and forkhead box P3-positive (FOXP3+) and PD-L1 expression in primary tumor tissue using immunohistochemistry and the clinical outcomes in 2 patient cohorts at the National Cancer Center: 256 patients diagnosed with early-stage BC from January 2001 to December 2005 and 77 hormone receptor (HR)-negative BC patients diagnosed from January 2006 to December 2008. Clinical data were collected, including HR status, human epidermal growth factor receptor 2 expression, disease-free survival, and overall survival (OS).
The median patient age was 47 years (range, 28-78), and the median follow-up period was 9.8 years. Of the 333 patients, 186 (55.9%) had HR-positive and 125 (37.5%) had node-positive BC. We found a strong positive correlation between CD8+ TILs and FOXP3+ TILs (P < .001). CD8+ TILs were more abundant in tumors with low PD-L1 expression (P < .001), although no association was found between FOXP3+ TILs and PD-L1 expression. More CD8+ TILs were present in HR-negative than in HR-positive BC (P < .001), and PD-L1 expression was more frequent in HR-positive BC (P < .001). A greater number of CD8+ TILs (increase in quartile) was strongly associated with OS (hazard ratio, 0.61; 95% confidence interval, 0.39-0.95; P = .03) only in HR-negative BC when adjusted for various clinical factors. PD-L1 expression and FOXP3+ TILs did not exhibit such associations.
Higher CD8+ lymphocyte infiltration was related to lower PD-L1 expression and higher FOXP3+ TIL infiltration in BC. Higher CD8+ TIL expression was associated with prolonged survival only in those with HR-negative BC.
免疫系统可能影响乳腺癌(BC)的预后。然而,关于BC亚型,程序性死亡配体1(PD-L1)与肿瘤浸润淋巴细胞(TIL)特征之间的关系仍不清楚。
我们使用免疫组织化学研究了原发性肿瘤组织中CD8 +和叉头框P3阳性(FOXP3 +)的TIL特征与PD-L1表达之间的关系,以及美国国立癌症中心2个患者队列的临床结局:2001年1月至2005年12月诊断为早期BC的256例患者,以及2006年1月至2008年12月诊断的77例激素受体(HR)阴性BC患者。收集了临床数据,包括HR状态、人表皮生长因子受体2表达、无病生存期和总生存期(OS)。
患者中位年龄为47岁(范围28 - 78岁),中位随访期为9.8年。在333例患者中,186例(55.9%)为HR阳性,125例(37.5%)为淋巴结阳性BC。我们发现CD8 + TIL与FOXP3 + TIL之间存在强正相关(P <.001)。CD8 + TIL在PD-L1低表达的肿瘤中更为丰富(P <.001),尽管未发现FOXP3 + TIL与PD-L1表达之间存在关联。HR阴性BC中的CD8 + TIL比HR阳性BC中的更多(P <.001),且PD-L1表达在HR阳性BC中更常见(P <.001)。仅在HR阴性BC中,当对各种临床因素进行校正后,更多的CD8 + TIL(四分位数增加)与OS密切相关(风险比,0.61;95%置信区间,0.39 - 0.95;P =.03)。PD-L1表达和FOXP3 + TIL未表现出此类关联。
在BC中,较高的CD8 +淋巴细胞浸润与较低的PD-L1表达及较高的FOXP3 + TIL浸润相关。仅在HR阴性BC患者中,较高的CD8 + TIL表达与生存期延长相关。