Department of Pathology, Anhui Medical University, Hefei, Anhui, 230032, People's Republic of China.
Department of Pathology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, 230022, People's Republic of China.
BMC Cancer. 2019 Nov 6;19(1):1049. doi: 10.1186/s12885-019-6208-x.
Diffuse large B-cell lymphoma (DLBCL) is characterized by its clinical and biological heterogeneity. The clinical prognostic implications of tumor-associated macrophages (TAMs) in DLBCL remain controversial and the correlation between TAMs and peripheral absolute monocyte count (AMC) has not yet been elucidated.
In 221 untreated, newly diagnosed patients with DLBCL, we evaluated the prognostic value of TAMs using immunohistochemical analysis, as well as the association of TAMs and AMC.
We found that high CD68 or high CD163 expression was correlated with clinicopathological characteristics, high CD163 expression was an adverse predictor for both overall survival (OS) [hazard ratio (HR) = 2.265, P = 0.005] and progression- free survival (PFS) (HR = 1.925, P = 0.017) in patients with DLBCL. Patients with high CD68 or high CD163 expression had significantly poorer OS and PFS than those with low CD68 or low CD163 expression, respectively (CD68: OS: P<0.001, PFS: P<0.001; CD163: OS: P<0.001, PFS: P<0.001), even in the rituximab era. Moreover, high-risk patients could be further identified by the expression of CD68 or CD163, especially in those classified as low/intermediate risk by International Prognostic Index (IPI). Furthermore, the significant positive correlation was also detected between CD68 expression or CD163 expression and AMC (r = 0.256, P<0.001; r = 0.303, P<0.001).
Patients with high expression of TAMs tend to have poorer OS and PFS, even in the rituximab era, and have positive correlation with AMC. Therefore, the peripheral AMC is a useful prognostic marker reflecting the status of the tumor microenvironment (TME) in DLBCL.
弥漫性大 B 细胞淋巴瘤(DLBCL)的临床和生物学表现具有异质性。肿瘤相关巨噬细胞(TAMs)在 DLBCL 中的临床预后意义仍存在争议,且 TAMs 与外周血绝对单核细胞计数(AMC)之间的相关性尚未阐明。
在 221 例未经治疗的新诊断 DLBCL 患者中,我们通过免疫组织化学分析评估了 TAMs 的预后价值,并研究了 TAMs 与 AMC 的相关性。
我们发现高 CD68 或高 CD163 表达与临床病理特征相关,高 CD163 表达是 DLBCL 患者总生存(OS)[风险比(HR)=2.265,P=0.005]和无进展生存(PFS)(HR=1.925,P=0.017)的不良预测因素。高 CD68 或高 CD163 表达的患者的 OS 和 PFS 明显差于低 CD68 或低 CD163 表达的患者(CD68:OS:P<0.001,PFS:P<0.001;CD163:OS:P<0.001,PFS:P<0.001),即使在利妥昔单抗时代也是如此。此外,还可以通过 CD68 或 CD163 的表达进一步确定高危患者,特别是那些按国际预后指数(IPI)分类为低/中危的患者。此外,还检测到 CD68 表达或 CD163 表达与 AMC 之间存在显著的正相关(r=0.256,P<0.001;r=0.303,P<0.001)。
高 TAMs 表达的患者 OS 和 PFS 较差,即使在利妥昔单抗时代也是如此,并且与 AMC 呈正相关。因此,外周血 AMC 是反映 DLBCL 肿瘤微环境(TME)状态的有用预后标志物。