Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Department of Pathology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Breast Cancer Res. 2024 May 8;26(1):75. doi: 10.1186/s13058-024-01831-8.
Tumor-associated macrophages (TAMs) are a prominent immune subpopulation in the tumor microenvironment that could potentially serve as therapeutic targets for breast cancer. Thus, it is important to characterize this cell population across different tumor subtypes including patterns of association with demographic and prognostic factors, and breast cancer outcomes.
We investigated CD163 macrophages in relation to clinicopathologic variables and breast cancer outcomes in the Women's Circle of Health Study and Women's Circle of Health Follow-up Study populations of predominantly Black women with breast cancer. We evaluated 611 invasive breast tumor samples (507 from Black women, 104 from White women) with immunohistochemical staining of tissue microarray slides followed by digital image analysis. Multivariable Cox proportional hazards models were used to estimate hazard ratios for overall survival (OS) and breast cancer-specific survival (BCSS) for 546 cases with available survival data (median follow-up time 9.68 years (IQR: 7.43-12.33).
Women with triple-negative breast cancer showed significantly improved OS in relation to increased levels of tumor-infiltrating CD163 macrophages in age-adjusted (Q3 vs. Q1: HR = 0.36; 95% CI 0.16-0.83) and fully adjusted models (Q3 vs. Q1: HR = 0.30; 95% CI 0.12-0.73). A similar, but non-statistically significant, association was observed for BCSS. Macrophage infiltration in luminal and HER2+ tumors was not associated with OS or BCSS. In a multivariate regression model that adjusted for age, subtype, grade, and tumor size, there was no significant difference in CD163 macrophage density between Black and White women (RR = 0.88; 95% CI 0.71-1.10).
In contrast to previous studies, we observed that higher densities of CD163 macrophages are independently associated with improved OS and BCSS in women with invasive triple-negative breast cancer. Trial registration Not applicable.
肿瘤相关巨噬细胞(TAMs)是肿瘤微环境中一种突出的免疫亚群,可能成为乳腺癌的治疗靶点。因此,对不同肿瘤亚型中的这种细胞群进行特征描述很重要,包括与人口统计学和预后因素以及乳腺癌结局的关联模式。
我们在黑人女性为主的妇女健康研究和妇女健康随访研究人群的 611 例浸润性乳腺癌肿瘤样本(507 例来自黑人女性,104 例来自白人女性)中,通过组织微阵列切片的免疫组织化学染色,然后进行数字图像分析,调查 CD163 巨噬细胞与临床病理变量和乳腺癌结局的关系。对于有可用生存数据的 546 例病例(中位随访时间 9.68 年(IQR:7.43-12.33)),使用多变量 Cox 比例风险模型估计总生存(OS)和乳腺癌特异性生存(BCSS)的风险比。
在调整年龄后(Q3 与 Q1:HR=0.36;95%CI 0.16-0.83)和完全调整模型中(Q3 与 Q1:HR=0.30;95%CI 0.12-0.73),三阴性乳腺癌女性的 OS 与肿瘤浸润性 CD163 巨噬细胞水平升高显著相关,差异具有统计学意义。BCSS 也观察到类似但无统计学意义的相关性。在 luminal 和 HER2+肿瘤中,巨噬细胞浸润与 OS 或 BCSS 无关。在一个调整年龄、亚型、分级和肿瘤大小的多变量回归模型中,黑人和白人女性的 CD163 巨噬细胞密度无显著差异(RR=0.88;95%CI 0.71-1.10)。
与以往研究不同,我们观察到在浸润性三阴性乳腺癌女性中,CD163 巨噬细胞密度较高与 OS 和 BCSS 独立相关。
试验注册 不适用。