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:Platinum-based systematic therapy in triple-negative breast cancer.
Platinum-based systematic therapy in triple-negative breast cancer.
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由于缺乏明确的激素受体,三阴性乳腺癌(TNBC)患者从内分泌治疗或分子靶向治疗中获得的临床获益甚微,导致该病具有高度侵袭性、高复发率和不良预后。过去几十年中,化疗一直是TNBC的主要治疗手段,以紫杉类/蒽环类方案为代表。
然而,蒽环类药物日益增加且不可逆的心脏毒性以及耐药问题不容忽视。逐渐地,以铂类为基础的化疗成为研究者关注的热点。基于越来越多关于含铂方案治疗TNBC患者的研究,我们将总结相关临床试验的进展,重点关注铂类单药治疗(如顺铂、卡铂和奥沙利铂)或与其他治疗方式联合(如其他化疗药物、分子靶向治疗和免疫治疗)。为进一步评估患者对铂类的反应并筛选出最能从铂类治疗中获益的最佳人群,我们还将分析当前潜在的生物标志物,如乳腺癌易感基因(BRCA1/2)、同源重组修复缺陷(HRD)、TIL(肿瘤浸润淋巴细胞)(TILs)、TP53家族及其他新兴指标(如内在亚型、细胞周期蛋白依赖性激酶2(CDK2)表达、血管内皮生长因子(VEGF)和基质金属蛋白酶-9(MMP-9))。
Due to the lack of definitive hormone receptors, triple negative breast cancer (TNBC) patients receive little clinical benefit from endocrine or molecular targeted therapies, leading to a highly aggressive disease with a high recurrence rate and poor prognosis. In the past decades, chemotherapy has been the mainstay of treatment for TNBC, with taxane/anthracyclines as the representative regimen.
However, increasing irreversible cardiotoxicity of anthracyclines and drug-resistance had to be noticed. Gradually, platinum-based chemotherapy has become a topic of interest for researchers. Based on the accumulating studies on platinum-containing regimens for TNBC patients, we will summarize the progress of relevant clinical trials focusing on platinum monotherapy (e. g. , cisplatin, carboplatin and oxaliplatin) or in combination with other therapeutic modalities (e. g. , other chemotherapeutic agents, molecular targeted therapies and immunotherapy).
To further evaluate patient response to platinum and screen for the optimal population to benefit from platinum, we will also analyze current potential biomarkers, such as breast cancer susceptibility genes (BRCA1/2), homologous recombination repair deficiency (HRD), tumor infiltrating lymphocytes (TILs), TP53 family and other emerging indicators (e. g. , intrinsic subtype, cyclin-dependent kinase 2 (CDK2) expression, vascular endothelial growth factor (VEGF) and matrix metalloproteinase-9 (MMP-9)).
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