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:Tumor infiltrating lymphocytes profile and response in neoadjuvant chemotherapy-treated triple-negative breast carcinoma patients.
Tumor infiltrating lymphocytes profile and response in neoadjuvant chemotherapy-treated triple-negative breast carcinoma patients.
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TIL 谱中 CD3、CD4、CD20 和 CD56 低表达可预测 TNBC 对 NACT 的 PR,因此可能有助于这些患者的预后判断。
三阴性乳腺癌(TNBC)在所有乳腺癌亚型中死亡率最高,但矛盾的是,它对新辅助化疗(NACT)的反应最好。TIL(肿瘤浸润淋巴细胞)密度已被证明在TNBC中具有预后意义。然而,关于TNBC中TIL亚群及其与NACT反应相关性的数据有限。
该研究前瞻性纳入了两年半内连续诊断的80例TNBC患者,这些患者在NACT前接受了tru-cut活检,随后接受了最终确定性手术。对所有基线tru-cut活检标本和NACT后手术标本进行了整体TIL特征分析以及CD3、CD4、CD8、CD20和CD56的免疫组织化学(IHC)分析。
近一半患者为绝经后女性,平均年龄为45.89 4.62岁。大多数患者在NACT前和NACT后标本中均表现为低CD3、低CD4、低CD56、低CD20和高CD8阳性。在多因素分析中,低CD3、CD4、CD56和CD20被确立为不良病理反应(PR)的独立预测因素。低CD4(调整比值比[OR]:228.46)与不良PR的最高OR相关。低CD8在单因素分析中与不良PR的比值比显著降低相关(OR:0.26),但在多因素logistic回归中未被确立为PR的独立预测因素。NACT未显著改变TILs的分布特征。
Triple negative breast carcinoma (TNBC) has the highest mortality among all the breast carcinoma subtypes, but paradoxically, it shows the best response to neoadjuvant chemotherapy (NACT). Tumor infiltrating lymphocytes (TIL) density has been shown to have prognostic significance in TNBC. However, there are limited data on TIL subpopulation and their association with response to NACT in TNBC.
The study included 80 consecutive patients with TNBC prospectively diagnosed for two and half years, who underwent tru-cut biopsy before NACT, followed by subsequent definite surgical procedures. Global TIL profile and immunohistochemistry (IHC) analysis of CD3, CD4, CD8, CD20, and CD56 were done on all baseline tru-cut biopsies and post-NACT surgical specimens.
Almost half the patients were postmenopausal with a mean age of 45.89 4.62 years. The majority had low CD3, low CD4, low CD56, low CD20, and high CD8 positivity in both pre- and post-NACT specimens. On multivariate analysis, low CD3, CD4, CD56 and CD 20 were established as independent predictor of poor pathologic response (PR). Low CD4 (adjusted odds ratio [OR]: 228.46) was associated with the highest OR for poor PR. Low CD8 was associated with significantly decreased odds of poor PR on univariate analysis (OR: 0.26), but it was not been established as an independent predictor of PR on multivariate logistic regression. NACT did not significantly alter the profile of TILs.
TIL profile with low CD3, CD4, CD20, and CD56 expression predicts PR to NACT in TNBC and may thus help in prognostication of these patients.
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