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 and mammographic density as predictors of response to neoadjuvant systemic therapy in breast cancer.
Evaluation of tumor-infiltrating lymphocytes and mammographic density as predictors of response to neoadjuvant systemic therapy in breast cancer.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
TILs 可显著预测 NAST 应答。
接受新辅助系统治疗(NAST)的乳腺癌患者缓解率各异,因此需要可靠的疗效预测指标。已有证据提示,TIL(肿瘤浸润淋巴细胞)可预测NAST应答,但临床上很少将其用于治疗决策。乳腺X线摄影致密度(MD)也是一种潜在的NAST获益标志物,但其与TIL的关系尚不清楚。本研究旨在评估TIL和MD对NAST应答的预测价值,并考察二者之间尚未研究的关联。
研究分析了2013至2020年接受NAST的315例浸润性乳腺癌。临床病理数据取自病历。终点定义为乳腺病理完全缓解(pCR)。评估治疗前空芯针活检中的TIL,并分为高水平(≥10%)和低水平(<10%)。根据乳腺影像报告和数据系统(BI-RADS)第五版将MD评分为a至d级。使用SPSS进行二元Logistic回归及Spearman相关检验。
315例癌症中,136例达到pCR;94例TIL水平高,215例低,6例缺少TIL数据。BI-RADS a、b、c、d级病例数分别为37、122、112和44。与低TIL相比,高TIL与pCR独立相关(OR=2.95;95%置信区间[CI]:1.59–5.46)。单变量分析中,MD(BI-RADS d级对比a级)显示pCR可能性较高的趋势(OR=2.43;95% CI:0.99–5.98),但关联无统计学意义,多变量分析结果亦一致(OR=2.51;95% CI:0.78–8.04)。TIL与MD之间未见相关性(相关系数0.02;p=0.80)。
TIL可显著预测NAST应答。本研究未能确认MD是NAST应答的显著预测指标;这些发现仍需进一步重复验证。
Response rates vary among breast cancer patients treated with neoadjuvant systemic therapy (NAST). Thus, there is a need for reliable treatment predictors. Evidence suggests tumor-infiltrating lymphocytes (TILs) predict NAST response. Still, TILs are seldom used clinically as a treatment determinant. Mammographic density (MD) is another potential marker for NAST benefit and its relationship with TILs is unknown. Our aims were to investigate TILs and MD as predictors of NAST response and to study the unexplored relationship between TILs and MD. MATERIAL AND METHODS: We studied 315 invasive breast carcinomas treated with NAST between 2013 and 2020. Clinicopathological data were retrieved from medical records. The endpoint was defined as pathological complete response (pCR) in the breast. TILs were evaluated in pre-treatment core biopsies and categorized as high ( 10%) or low (<10%). MD was scored ( a - d ) according to the breast imaging reporting and data system (BI-RADS) fifth edition. Binary logistic regression and Spearman's test of correlation were performed using SPSS.
Out of 315 carcinomas, 136 achieved pCR. 94 carcinomas had high TILs and 215 had low TILs. Six carcinomas had no available TIL data. The number of carcinomas in each BI-RADS category were 37, 122, 112, and 44 for a , b , c , and d , respectively. High TILs were independently associated with pCR (OR: 2.95; 95% CI: 1.59-5.46) compared to low TILs. In the univariable analysis, MD (BI-RADS d vs. a ) showed a tendency of higher likelihood for pCR (OR: 2.43; 95% CI: 0.99-5.98). However, the association was non-significant, which is consistent with the result of the multivariable analysis (OR: 2.51; 95% CI: 0.78-8.04). We found no correlation between TILs and MD (0.02; p = .80).
TILs significantly predicted NAST response. We could not define MD as a significant predictor of NAST response. These findings should be further replicated.
MEMBER ACCOUNT
登录成功会直接打开下一页。