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:Elasticity Values as a Predictive Modality for Response to Neoadjuvant Chemotherapy in Breast Cancer.
Elasticity Values as a Predictive Modality for Response to Neoadjuvant Chemotherapy in Breast Cancer.
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剪切波弹性成像(SWE)是鉴别乳腺癌恶性病灶及腋窝淋巴结转移的有效工具。然而,乳腺癌基线弹性值与新辅助化疗治疗反应之间的关联尚未阐明。基线SWE测量了2012年1月至2022年12月期间接受新辅助化疗和手术的830例患者的平均硬度(E-mean)和最大硬度(E-max)。分析了弹性值与乳腺pCR(定义为ypTis/T0)、pCR(定义为ypTis/T0,N0)及TIL(肿瘤浸润淋巴细胞)(TILs)的关联。在830例患者中,356例(42.9%)达到乳腺pCR,324例(39.0%)达到pCR。低弹性值患者的乳腺pCR率和pCR率高于高弹性值患者。低E-mean(调整后比值比(OR):0.620;95%置信区间(CI):0.437至0.878;p = 0.007)和低E-max(调整后OR:0.701;95% CI:0.494至0.996;p = 0.047)是乳腺pCR的独立预测因素。低弹性值与高TILs显著相关。使用SWE测量的治疗前弹性值与治疗反应显著相关,并与TILs呈负相关,尤其是在HR+HER2-乳腺癌和TNBC中。
Shear-wave elastography (SWE) is an effective tool in discriminating malignant lesions of breast and axillary lymph node metastasis in patients with breast cancer.
However, the association between the baseline elasticity value of breast cancer and the treatment response of neoadjuvant chemotherapy is yet to be elucidated. Baseline SWE measured mean stiffness (E-mean) and maximum stiffness (E-max) in 830 patients who underwent neoadjuvant chemotherapy and surgery from January 2012 to December 2022. Association of elasticity values with breast pCR (defined as ypTis/T0), pCR (defined as ypTis/T0, N0), and tumor-infiltrating lymphocytes (TILs) was analyzed. Of 830 patients, 356 (42. 9%) achieved breast pCR, and 324 (39. 0%) achieved pCR.
The patients with low elasticity values had higher breast pCR and pCR rates than those with high elasticity values. A low E-mean (adjusted odds ratio (OR): 0. 620; 95% confidence interval (CI): 0. 437 to 0. 878; p = 0. 007) and low E-max (adjusted OR: 0. 701; 95% CI: 0. 494 to 0. 996; p = 0.
047) were independent predictive factors for breast pCR. Low elasticity values were significantly correlated with high TILs. Pretreatment elasticity values measured using SWE were significantly associated with treatment response and inversely correlated with TILs, particularly in HR+HER2- breast cancer and TNBC.
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