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:Association of tumor-infiltrating lymphocytes with clinical outcomes in patients with triple-negative breast cancer receiving neoadjuvant chemotherapy: a systematic review and meta-analysis.
Association of tumor-infiltrating lymphocytes with clinical outcomes in patients with triple-negative breast cancer receiving neoadjuvant chemotherapy: a systematic review and meta-analysis.
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TNBC 患者中 TILs 表达较高与 DFS、OS 和 pCR 结局显著改善相关。
三阴性乳腺癌(TNBC)作为一种侵袭性肿瘤,与不良预后相关,构成临床挑战。TIL(肿瘤浸润淋巴细胞)(TILs)作为潜在的预后生物标志物已引起关注。然而,不同TILs水平之间结局的差异仍未得到充分探索。
检索了PubMed、Scopus、Web of Science和Cochrane数据库,以寻找关于TILs在接受新辅助化疗的TNBC患者中预后价值的研究。对二分类终点计算了风险比(HRs)或比值比(ORs),并给出了95%置信区间(CIs)。
共纳入29项研究,涉及6161例(80.41%)TNBC患者。TILs的截断值范围为10%至60%,其中50%是最相关的数值。与低TIL表达组相比,高TIL浸润组的无病生存期(DFS)(HR 0.71;95% CI 0.61-0.82;p < 0.00001)和总生存期(OS)(HR 0.76;95% CI 0.63-0.90;p = 0.002)率显示出显著改善。在淋巴细胞亚型CD4+和CD8+的亚组分析中,两种亚型均显示较高的TILs率具有统计学意义,分别与DFS改善(HR 0.48;95% CI 0.33-0.71;p = 0.0002)和OS改善(HR 0.53;95% CI 0.36-0.78;p = 0.001)相关,无论哪种细胞亚型占主要浸润成分。完全病理缓解分析显示,在TIL(OR 1.29;95% CI 1.13-1.48;p = 0.0003)和Ki-67(OR 2.74;95% CI 2.01-3.73;p < 0.00001)分析中,高TIL组的缓解率均优于对照组。
Triple-negative breast cancer (TNBC) presents a clinical challenge as an aggressive tumor, correlated with unfavorable prognosis. Tumor-infiltrating lymphocytes (TILs) have garnered interest as a potential prognostic biomarker. However, the disparity in outcomes between varying TILs rates remains inadequately explored.
PubMed, Scopus, Web of Science, and Cochrane databases were searched for studies about the prognostic value of TILs in patients with TNBC receiving neoadjuvant chemotherapy. The hazard ratios (HRs) or odds ratios (ORs) were computed for binary endpoints, with 95% confidence intervals (CIs).
Twenty-nine studies were included, involving a population of six thousand one hundred sixty-one (80.41%) with TNBC. The cut-off TILs value ranged from 10 to 60%, with 50% being the most related value. Compared with the low-TIL expression group, the disease-free survival (DFS) (HR 0.71; 95% CI 0.61-0.82; p < 0.00001) and overall survival (OS) (HR 0.76; 95% CI 0.63-0.90; p = 0.002) rates showed significant improvement with higher TIL infiltrations. In the subgroup analyses of the lymphocyte subtypes CD4 + and CD8 + , there was statistical significance favoring higher TILs rates in both subtypes, each associated with improved DFS (HR 0.48; 95% CI 0.33-0.71; p = 0.0002) and OS (HR 0.53; 95% CI 0.36-0.78; p = 0.001), regardless of which cell subtype was predominantly infiltrated. The complete pathological response analysis showed better rates for the higher TIL group than the control for both the TIL (OR 1.29; 95% CI 1.13-1.48; p = 0.0003) and Ki-67 (OR 2.74; 95% CI 2.01-3.73; p < 0.00001) analyses.
Higher expressions of TILs in patients with TNBC were associated with improved significantly DFS, OS, and pCR outcomes.
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