Correlation of 18F-FDG PET/CT metabolic parameters with Ki-67 expression and tumor staging in nasopharyngeal carcinoma.

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Tác giả: ChengMao Guo, MeiNa Liang, JunJia Luo, JingXing Xiao

Ngôn ngữ: eng

Ký hiệu phân loại: 005.756 Relational databases

Thông tin xuất bản: England : Nuclear medicine communications , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 208963

 PURPOSE: The study aimed to investigate the imaging parameters of 18F-fluorodeoxyglucose (18F-FDG) PET/computed tomography (PET/CT) in nasopharyngeal carcinoma (NPC), specifically examining the relationship between mean standardized uptake value (SUVmean), maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) with Ki-67 expression, T-stage, and tumor node metastasis (TNM) stage. METHODS: A retrospective analysis was conducted on 143 consecutive NPC patients from January 2015 to December 2023 who underwent 18F-FDG PET/CT for initial disease assessment. SUVmax, SUVmean, MTV, and TLG were quantified from PET/CT images. Immunohistochemical staining was used to assess Ki-67 protein expression. Correlations between 18F-FDG PET/CT metabolic parameters, Ki-67 expression, T-stage, and TNM-stage were evaluated using statistical methods, with significance set at P <
  0.05. RESULTS: All primary NPC lesions demonstrated elevated 18F-FDG uptake. Significant positive correlations were observed between SUVmax (r = 0.234, P = 0.005), SUVmean (r = 0.223, P = 0.007), MTV (r = 0.218, P = 0.009), and TLG (r = 0.232, P = 0.005) with Ki-67 labeling index. The univariate analysis indicated that all the parameters (SUVmax, SUVmean, MTV, and TLG) in the group with Ki-67 ≥ 50% were significantly higher than those in the group with Ki-67 <
  50% (P = 0.001). Additionally, binary logistic regression analysis revealed that SUVmax was an independent risk factor for the group with Ki-67 ≥ 50% (P = 0.003). The univariate analysis revealed that all parameters (SUVmax, SUVmean, MTV, and TLG) in the T3-4 group and clinical stage IV group were significantly higher than those in the T1-2 group and stages I-III group (P both <
 0.05), respectively. Furthermore, binary logistic regression analysis demonstrated that MTV was an independent risk factor for both comparisons (P both <
 0.05). CONCLUSION: The metabolic parameters derived from 18F-FDG PET/CT in NPC indirectly reflect tumor biological behavior, suggesting their potential utility in guiding individualized comprehensive treatment strategies.
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