再分化使能的 TSHRCART 细胞克服侵袭性甲状腺癌中的抗原丢失
Redifferentiation-enabled TSHRCART cells overcome antigen loss in aggressive thyroid cancers.
这些发现确立了肿瘤再分化作为一种可推广的策略,用于克服抗原丢失并增强 CAR-T 细胞疗法在甲状腺癌以及可能其他实体瘤中的疗效。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Predictive and prognostic value of aurora kinase A combined with tumor-infiltrating lymphocytes in medullary thyroid carcinoma.
Predictive and prognostic value of aurora kinase A combined with tumor-infiltrating lymphocytes in medullary thyroid carcinoma.
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AURKA 高表达与 MTC 恶性程度相关。
既往研究提示,Aurora激酶A(AURKA)和TIL(肿瘤浸润淋巴细胞)均参与肿瘤发生发展,但其在甲状腺髓样癌中的表达及预后价值尚未明确。本研究收集137例患者的手术标本和临床资料,通过免疫组化及苏木精-伊红染色评估AURKA表达和TIL浸润。AURKA在多灶肿瘤、颈部淋巴结转移和晚期TNM分期患者中高表达,并与TIL呈正相关。AURKA高表达且TIL较低是生化复发及无复发生存的独立预后因素。两者联合可改善对生化和结构性复发的预测能力,并能较准确预测远处或不可切除的局部区域复发。结果提示,AURKA高表达与甲状腺髓样癌恶性程度相关,AURKA高表达/TIL低水平组合可能成为预测难治性复发的新型独立标志物。
Aurora kinase A (AURKA) and tumor-infiltrating lymphocytes (TILs) are both known to play an essential role in tumorigenesis. However, the expression and prognostic value of the AURKA and TILs in medullary thyroid carcinoma (MTC) have not yet been investigated.
Surgical specimens and clinical data of 137 patients diagnosed with MTC were collected. AURKA expression and TILs infiltration were quantified by immunohistochemistry and hematoxylin-eosin staining. Subsequently, the prognostic value of AURKA expression and TIL infiltration in MTC was evaluated.
AURKA was highly expressed in patients with multifocal tumor, cervical lymph node metastasis, and an advanced TNM stage, indicating a high probability of recurrence. AURKA further exhibited a positive correlation with TILs (R = 0.44, P < 0.001). High expression of AURKA combined with a low numbers of TILs (AURKA high /TILs low ) was identified as an independent prognostic factor for biochemical recurrence (odds ratio: 4.57, 95% confidence interval: 1.54-14.66, P < 0.01) and recurrence-free survival (hazard ratio: 3.64, 95% confidence interval: 1.52-8.71, P < 0.001). The combination of AURKA and TILs apparently improves the prognostic value for biochemical recurrence (area under the curve: 0.751) and structural recurrence (area under the curve: 0.836) of MTC. Notably, AURKA high /TILs low demonstrated a high value for prediction of distant or unresectable locoregional recurrence, with an overall accuracy of 86.9%.
AURKA high is associated with the MTC malignancy. The combination of AURKA high /TILs low was identified as novel independent prognostic marker in MTC, predicting incurable disease recurrence with high accuracy.
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