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:New Emerging Chemokine Receptors: CCR5 or CXCR5 on Tumor Is Associated with Poor Response to Chemotherapy and Poor Prognosis in Locally Advanced Triple-Negative Breast Cancer.
New Emerging Chemokine Receptors: CCR5 or CXCR5 on Tumor Is Associated with Poor Response to Chemotherapy and Poor Prognosis in Locally Advanced Triple-Negative Breast Cancer.
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在本局部晚期 TNBC 队列中,发现 CXCR4 TM 和 CCR5 TM 高表达与不良预后相关,而 CXCR5 TM 与化疗反应差相关。
本研究评估局部晚期三阴性乳腺癌患者趋化因子受体表达与新辅助化疗反应及结局的关系。
对63例手术标本进行免疫组化,检测CCR5、CCR7、CXCR4和CXCR5。
肿瘤中上述受体高表达及TIL中CXCR4高表达者,达到病理完全缓解或低残留癌负荷等级的可能性较低。存在残余淋巴结转移且肿瘤CCR5或CXCR4高表达者,疾病无复发生存和疾病特异性生存风险较高;反之,TIL中未表达CXCR5者风险也升高。
本队列中肿瘤CXCR4和CCR5高表达与不良预后相关,CXCR5肿瘤表达与较差化疗反应相关。结果提示,在新辅助化疗方案中加入趋化因子受体抑制剂可能使部分三阴性乳腺癌患者获益。
We aim to investigate any possible associations between chemokine receptor expression and responses to neoadjuvant chemotherapy (NAC) along with outcomes in patients with triple-negative breast cancer (TNBC) with locally advanced disease. METHOD: Expressions of chemokine receptors were examined immunohistochemically after staining archival tissue of surgical specimens (n = 63) using specific antibodies for CCR5, CCR7, CXCR4, and CXCR5.
Patients with high CCR5, CCR7, CXCR4, and CXCR5 expression on tumors and high CXCR4 expression on tumor-infiltrating lymphocytes (TILs) were less likely to have a pathological complete response (pCR) or Class 0-I RCB-Index compared to others. Patients with residual lymph node metastases (ypN-positive), high CCR5 TM(tumor) , and high CXCR4 TM expressions had an increased hazard ratio (HR) compared to others (DFS: HR = 2.655 [1.029-6.852]; DSS: HR = 2.763 [1.008-7.574]), (DFS: HR = 2.036 [0.805-5.148]; DSS: HR = 2.689 [1.020-7.090]), and (DFS: HR = 2.908 [1.080-7.829]; DSS: HR = 2.132 (0.778-5.846)), respectively. However, patients without CXCR5 TIL expression had an increased HR compared to those with CXCR5 TIL (DFS: 2.838 [1.266-6.362]; DSS: 4.211 [1.770-10.016]).
High expression of CXCR4 TM and CCR5 TM was found to be associated with poor prognosis, and CXCR5 TM was associated with poor chemotherapy response in the present cohort with locally advanced TNBC. Our results suggest that patients with TNBC could benefit from a chemokine receptor inhibitor therapy containing neoadjuvant chemotherapy protocols.
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