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:Prognostic significance of CD8 + tumor-infiltrating lymphocytes in operable breast cancer: a meta-analysis.
Prognostic significance of CD8 + tumor-infiltrating lymphocytes in operable breast cancer: a meta-analysis.
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乳腺癌患者中高 CD8⁺ TIL 密度与良好预后相关,与 CD8⁺ TIL(肿瘤浸润淋巴细胞)的位置无关。
CD8⁺ TIL(肿瘤浸润淋巴细胞)是抗肿瘤免疫的重要介导者,可呈递抗原并启动针对癌细胞的强效免疫应答。按位置分层时,可将 CD8⁺ T 淋巴细胞计数并分为肿瘤内、间质或总 CD8⁺ TIL。尽管 CD8⁺ T 淋巴细胞作用关键,其对乳腺癌预后的影响,尤其不同位置亚型的作用,仍存在争议。本荟萃分析整合证据,明确不同计数方法评估的 CD8⁺ TIL 密度与乳腺癌患者结局之间的关系。
系统检索 PubMed、Embase 和 Cochrane Library 自建库至 2024 年 1 月发表的研究,纳入评估 CD8⁺ TIL 对乳腺癌预后意义的研究。主要终点为无病生存期(DFS);次要终点为总生存期(OS)、乳腺癌特异性生存(BCSS)和无复发生存(RFS)。
共纳入 34 项研究,涉及 23,626 例乳腺癌患者。合并风险比(HR)显示 CD8⁺ TIL 丰度高与 DFS(HR = 0.63;95% CI 0.54–0.73)、OS(HR = 0.72;95% CI 0.65–0.79)、BCSS(HR = 0.67;95% CI 0.58–0.78)和 RFS(HR = 0.53;95% CI 0.38–0.73)改善显著相关。按 TIL 位置(肿瘤内 iCD8、间质 sCD8 或总 tCD8)分层,未显著影响 DFS 或 OS。
乳腺癌患者 CD8⁺ TIL 密度较高与良好预后相关,不受 CD8⁺ TIL(肿瘤浸润淋巴细胞)位置影响。这些发现证实 CD8⁺ TIL 评估的预后价值,并可能指导未来免疫治疗策略。
As key mediators of antitumor immunity, CD8 + tumor-infiltrating lymphocytes present antigens and initiate robust immune responses against cancer cells. When stratified by location, CD8 + T lymphocytes were counted and classified as intratumoral, stromal, or total CD8 + tumor-infiltrating lymphocytes. Despite their crucial role, the impact, especially the specific type of CD8 + T lymphocytes on breast cancer prognosis remains controversial. This meta-analysis synthesized evidence to delineate the relationship between CD8 + tumor-infiltrating lymphocytes density of different counting methods and breast cancer patient outcomes.
PubMed, Embase, and the Cochrane Library were systemically searched from inception through January 2024 for studies evaluating the prognostic significance of CD8 + tumor-infiltrating lymphocytes in breast cancer. The primary endpoint was disease-free survival (DFS), and the second endpoints were overall survival (OS), breast cancer-specific survival (BCSS), and recurrence-free survival (RFS).
Thirty-four studies encompassing 23,626 breast cancer patients were included. Pooled hazard ratios (HRs) indicated a significant association of high CD8 + TIL presence with improved DFS (HR = 0.63; 95% CI = 0.54-0.73), OS (HR = 0.72; 95% CI = 0.65-0.79), BCSS (HR = 0.67; 95% CI = 0.58-0.78), and RFS (HR = 0.53; 95% CI = 0.38-0.73). Stratification by TIL location (intratumoral [iCD8], stromal [sCD8], or total [tCD8]) did not significantly impact DFS or OS.
High CD8 + TIL density in breast cancer patients is correlated with a favorable prognosis, irrespective of the location of CD8 + tumor-infiltrating lymphocytes. These findings affirm the prognostic utility of CD8 + TIL assessment and may guide future immunotherapeutic strategies.
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