Lu Xunxi, Wang Yue, He Mengting, Gou Zongchao
Department of Pathology, Sichuan University West China Hospital, Chengdu, Sichuan, China.
Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, Shanghai, China.
J Clin Pathol. 2024 Jan 18;77(2):128-134. doi: 10.1136/jcp-2022-208601.
The Glasgow Microenvironment Score (GMS) reflects the tumour microenvironment (TME) status by combining inflammatory cell infiltration and the tumour-stroma percentage. This study aimed to investigate the prognostic value and TME characteristics of the GMS for patients with triple-negative breast cancer (TNBC).
A total of 123 patients with stage I-III TNBC were enrolled in this study. The association between GMS and clinicopathological characteristics was examined using the Pearson's χ test or Fisher's exact test. Kaplan-Meier plots were used to compare survival among the three GMS groups. Cox regression analyses were conducted to test the HR. Microenvironment Cell Populations-counter algorithm was used to estimate the TME components of each case.
We found that higher GMS score tended to exhibit the lower nuclear grade (p=0.016), more positive lymph nodes (p=0.014) and later tumour, node, metastases stage (p=0.012). GMS was an independent prognostic factor for disease-free survival in TNBC, and GMS 2 showed the worst prognosis (HR=6.42, p=0.028). GMS 0 was more infiltrated with cytotoxic lymphocytes, including CD8+ T cells (p=0.037) and natural killer cells (p=0.005), while GMS 2 was enriched in more endothelial cells (p=0.014) and fibroblasts (p=0.008).
Our study suggested that the GMS is a prognostic indicator for patients with TNBC. As an accessible and effective index, the GMS may be a promising tool to help clinicians assess prognostic risk and TME for patients with TNBC.
格拉斯哥微环境评分(GMS)通过结合炎症细胞浸润和肿瘤-基质百分比来反映肿瘤微环境(TME)状态。本研究旨在探讨GMS对三阴性乳腺癌(TNBC)患者的预后价值和TME特征。
本研究共纳入123例I-III期TNBC患者。采用Pearson卡方检验或Fisher精确检验来检验GMS与临床病理特征之间的关联。使用Kaplan-Meier曲线比较三个GMS组之间的生存率。进行Cox回归分析以检验风险比(HR)。采用微环境细胞群体计数算法来估计每个病例的TME成分。
我们发现较高的GMS评分往往显示出较低的核分级(p = 0.016)、更多的阳性淋巴结(p = 0.014)和更晚的肿瘤、淋巴结、转移分期(p = 0.012)。GMS是TNBC患者无病生存的独立预后因素,GMS 2显示出最差的预后(HR = 6.42,p = 0.028)。GMS 0中细胞毒性淋巴细胞浸润更多,包括CD8 + T细胞(p = 0.037)和自然杀伤细胞(p = 0.005),而GMS 2中内皮细胞(p = 0.014)和成纤维细胞(p = 0.008)更丰富。
我们的研究表明,GMS是TNBC患者的预后指标。作为一种可获取且有效的指标,GMS可能是帮助临床医生评估TNBC患者预后风险和TME的有前景的工具。