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Density of tertiary lymphoid structures predicts clinical outcome in breast cancer brain metastasis

乳腺癌 细胞毒性T细胞 CD8型 医学 内科学 肿瘤科 免疫组织化学 递归分区 肿瘤浸润淋巴细胞 癌症 癌症研究 免疫疗法 免疫学 免疫系统 生物 生物化学 体外
作者
Yuanyuan Zhao,Zhen Fan,Baorui Tao,Zunguo Du,Zhifeng Shi
出处
期刊:Journal for ImmunoTherapy of Cancer [BMJ]
卷期号:12 (7): e009232-e009232
标识
DOI:10.1136/jitc-2024-009232
摘要

Background Patients with breast cancer brain metastases (BCBM) experience a rapid decline in their quality of life. Recently, tertiary lymphoid structures (TLSs), analogs of secondary lymphoid organs, have attracted extensive attention. However, the potential clinical implications of TLSs in BCBMs are poorly understood. In this study, we evaluated the density and composition of TLSs in BCBMs and described their prognostic value. Methods Clinicopathological data were collected from 98 patients (2015–2021). TLSs were evaluated, and a TLS scoring system was constructed. Differences in progression-free survival (PFS) and overall survival (OS) between groups were calculated using the Kaplan-Meier method. Immunohistochemistry and multiplex immunofluorescence (mIF) were used to assess TLSs heterogeneity. Results TLSs were identified in 47 patients with BCBM. High TLSs density indicated favorable survival (OS, p=0.003; PFS, p<0.001). TLS was positively associated with OS (p=0.0172) and PFS (p=0.0161) in the human epidermal growth factor receptor type 2-positive subtype, and with prolonged OS (p=0.0482) in the triple-negative breast cancer subtype. The mIF results showed significant differences in the percentages of T follicular helper (Tfh) cells, M2 macrophages, cytotoxic T lymphocytes, and CD8 + TIM-3 + T lymphocytes between the groups of TLS scores 0–3 (cytotoxic T lymphocytes, p=0.044; Tfh, p=0.021; M2 macrophages, p=0.033; CD8 + TIM-3 + T lymphocytes, p=0.018). Furthermore, novel nomograms incorporating the TLS scores and other clinicopathological predictors demonstrated prominent predictability of the 1-year, 3-year, and 5-year outcomes of BCBMs (area under the curve >0.800). Conclusion Our results highlight the impact of TLSs abundance on the OS and PFS of patients with BCBM. Additionally, we described the immune composition of TLSs and proposed novel nomograms to predict the prognosis of patients with BCBM.
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