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:Evaluating the correlation between pretreatment (18)F-FDG PET/CT metabolic parameters and tumor-infiltrating lymphocyte levels in nonluminal breast cancer and impact on survival.
Evaluating the correlation between pretreatment (18)F-FDG PET/CT metabolic parameters and tumor-infiltrating lymphocyte levels in nonluminal breast cancer and impact on survival.
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我们的研究表明,TIL、FDG 代谢参数与肿瘤异质性之间存在强关联,尤其是在晚期 NLBC 中。尽管 TIL 通常与 SUV 值无关,但其与某些代谢及异质性指数的关联提示,它在影响生存方面具有重要作用。需要开展纳入更大队列及多种乳腺癌亚型的进一步研究来验证这些结果。
本研究旨在评估非管腔型乳腺癌(NLBC)中TIL(肿瘤浸润淋巴细胞)水平与氟-18氟脱氧葡萄糖(18F-FDG)代谢参数(包括脾脏和骨髓FDG摄取及肿瘤异质性)之间的相关性,并阐明其与生存结局的关联。
我们回顾性分析了100例接受治疗前18F-FDG正电子发射断层扫描-计算机断层扫描(PET/CT)的2-4期NLBC女性患者的数据。TIL基于苏木精-伊红染色标本评分,并计算了18F-FDG PET代谢参数,包括最大标准化摄取值(SUVmax)、平均标准化摄取值(SUVmean)、代谢肿瘤体积(MTV)、总病灶糖酵解(TLG)、肝脏、脾脏和骨髓FDG摄取。异质性指数(HI)1、HI2和HI3指数与FDG代谢参数进行分析。这些因素与总生存期之间的关联使用多变量Cox回归模型进行分析。
TIL与肿瘤大小、肿瘤(T)和转移(M)分期呈弱负相关。TIL水平与总体SUV值之间未发现显著相关性。然而,在4期,TIL与肝脏、脾脏和骨髓SUV值呈正相关,与异质性指数(HI2、HI3)呈负相关。较大的肿瘤大小、较高的HI值和骨髓与肝脏比值(BLR) SUVmean与死亡率增加相关。TIL截断值<5与显著更差的生存相关。
We retrospectively analyzed data from 100 females with stage 2-4 NLBC who underwent pretreatment 18 F-FDG Positron emission tomography-computed tomography (PET/CT). TIL was scored based on Hematoxylin-Eosin-stained specimens and 18 F-FDG PET metabolic parameters, including maximum standardized uptake value (SUVmax), mean standardized uptake value (SUVmean), metabolic tumor volume (MTV), total lesion glycolysis (TLG), liver, spleen, and bone marrow FDG uptake were calculated. Heterogeneity Index (HI)1, HI2, and HI3 indices were analyzed with FDG metabolic parameters. The association between these factors and overall survival was analyzed using multivariate Cox regression models.
TIL showed weak negative correlations with tumor size, tumor (T), and metastasis (M) stages. No significant correlation was found between TIL levels and overall SUV values. However, in stage 4, TIL correlated positively with liver, spleen, and bone marrow SUV values and negatively with heterogeneity indices (HI2, HI3). Higher tumor size, HI values, and Bone marrow-to-liver ratio (BLR) SUVmean were associated with increased mortality. A TIL cut-off value of <5 was linked to significantly worse survival.
Our study demonstrates a strong connection between TIL, FDG metabolic parameters, and tumor heterogeneity, particularly in advanced NLBC. Although TIL is not generally associated with SUV values, its association with certain metabolic and heterogeneity indices suggests that it is important in influencing survival. Further research involving larger cohorts and diverse breast cancer subtypes is needed to validate these results.
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