基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Evaluation of tumor-infiltrating lymphocytes across breast cancer stages at the University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia.
Evaluation of tumor-infiltrating lymphocytes across breast cancer stages at the University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia.
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TIL 评分与 TNM 分期之间呈正相关。
TIL(肿瘤浸润淋巴细胞)已被认为是预后生物标志物。然而,乳腺癌不同分期的TIL评分并不一致,埃塞俄比亚患者相关数据也十分有限。因此,本研究评估埃塞俄比亚西北部乳腺癌各分期的TIL评分。
研究于2024年6月20日至2025年6月19日开展横断面分析。采用连续抽样纳入62例乳腺癌患者,通过问卷和病历审查收集社会人口学及临床病理资料。对福尔马林固定、石蜡包埋组织切片进行苏木精-伊红染色,并依据国际TIL工作组指南评估间质TIL。使用SPSS 27版分析数据。采用Kruskal-Wallis及Mann-Whitney U检验评估不同临床病理变量的TIL中位数,采用Spearman相关分析评估TIL评分与临床病理变量的关联。P<0.05为差异具有统计学意义。
II期病例中76.5%表现为低TIL评分;IV期病例中54.5%表现为高TIL评分。IV期(48%)和III期(33%)TIL中位百分比显著高于II期(7%);N2-N3(33%)也高于N0-N1(9%)(p<0.001)。此外,III级肿瘤的TIL中位百分比(48%)高于I级(9%)(p=0.028)。TIL与TNM分期、淋巴结分期及肿瘤分级呈正相关。
TIL评分与TNM分期呈正相关。中、高TIL评分常见于晚期,而低TIL评分多见于早期。结果提示晚期肿瘤可能具有较高突变负荷和免疫原性。未来研究应探讨免疫谱的分子亚型。
Tumor-infiltrating lymphocytes (TILs) are recognized as prognostic biomarkers. However, inconsistent TIL scores across breast cancer stages, and data are scarce for Ethiopian patients. Thus, this study evaluated TIL scores across breast cancer stages in Northwest Ethiopia.
A cross-sectional study was conducted from 20 June 2024 to 19 June 2025. Using consecutive sampling, 62 breast cancer patients were enrolled, and their socio-demographic and clinicopathological data were collected using questionnaires and chart reviews. Formalin-fixed, paraffin-embedded tissue sections were stained with hematoxylin and eosin, and stromal TILs were evaluated according to the International TIL Working Group guidelines. Data were analyzed using SPSS version 27. Median TILs across clinicopathological variables were assessed using Kruskal-Wallis and Mann-Whitney U tests. Spearman correlation assessed the association of TIL scores and clinicopathological variables. P 0.05 was considered statistically significant.
Low TIL scores were observed in 76.5% of stage II cases, whereas high TIL scores were observed in 54.5% of stage IV cases. Median TIL percentages in stage IV (48%) and III (33%) were significantly higher than in stage II (7%), and in N2-N3 (33%) than in N0-N1 (9%) (p < 0.001). Moreover, the median TIL percentage in grade III (48%) was higher than in grade I (9%) (p = 0.028). TILs were positively correlated with TNM stage, lymph node stage, and grade.
A positive correlation was found between TIL score and TNM stage. Intermediate and high TIL scores were common in advanced stages, whereas low TIL scores were prevalent in early stages. The findings suggest that advanced tumors may harbor higher mutation burdens and immunogenicity. Future research should explore the molecular subtypes of immune profiles.
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