Predictive value of 18F-FDG PET/CT multi-metabolic parameters and tumor metabolic heterogeneity in the prognosis of gastric cancer

被引:2
|
作者
Wang, Jianlin [1 ,2 ]
Yu, Xiaopeng [1 ,2 ]
Shi, Aiqi [3 ]
Xie, Long [1 ,2 ]
Huang, Liqun [1 ,2 ]
Su, Yingrui [1 ,2 ]
Zha, Jinshun [1 ,2 ]
Liu, Jiangyan [3 ]
机构
[1] Fujian Med Univ, Dept Nucl Med, Affiliated Hosp 2, Quanzhou 362018, Peoples R China
[2] Fujian Med Univ, Clin Sch 2, Affiliated Hosp 2, Quanzhou 362018, Peoples R China
[3] Lanzhou Univ, Dept Nucl Med, Hosp 2, Cuiyingmen 82, Lanzhou 730030, Peoples R China
关键词
Gastric cancer; F-18-FDG PET; CT; Metabolic parameters; Metabolic heterogeneity; Prognosis; POSITRON-EMISSION-TOMOGRAPHY; INTRATUMORAL HETEROGENEITY; FDG PET/CT; ANGIOGENESIS; METASTASIS; DEFINITION; NOMOGRAM; MRI;
D O I
10.1007/s00432-023-05246-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectiveWe aimed to investigate the predictive value of pre-treatment F-18-FDG PET/CT multi-metabolic parameters and tumor metabolic heterogeneity for gastric cancer prognosis.MethodsSeventy-one patients with gastric cancer were included. All patients underwent F-18-FDG PET/CT whole-body scans prior to treatment and had pathologically confirmed gastric adenocarcinomas. Each metabolic parameter, including SUVmax, SUVmean, MTV, and TLG, was collected from the primary lesions of gastric cancer in all patients, and the slope of the linear regression between the MTV corresponding to different SUVmax thresholds (40% x SUVmax, 80% x SUVmax) of the primary lesions was calculated. The absolute value of the slope was regarded as the metabolic heterogeneity of the primary lesions, expressed as the heterogeneity index HI-1, and the coefficient of variance of the SUVmean of the primary lesions was regarded as HI-2. Patient prognosis was assessed by PFS and OS, and a nomogram of the prognostic prediction model was constructed, after which the clinical utility of the model was assessed using DCA.ResultsA total of 71 patients with gastric cancer, including 57 (80.3%) males and 14 (19.7%) females, had a mean age of 61 & PLUSMN; 10 years; disease progression occurred in 27 (38.0%) patients and death occurred in 24 (33.8%) patients. Multivariate Cox regression analysis showed that HI-1 alone was a common independent risk factor for PFS (HR: 1.183; 95% CI: 1.010-1.387, P < 0.05) and OS (HR: 1.214; 95% CI: 1.016-1.450, P < 0.05) in patients with gastric cancer. A nomogram created based on the results of Cox regression analysis increased the net clinical benefit for patients. Considering disease progression as a positive event, patients were divided into low-, intermediate-, and high-risk groups, and Kaplan-Meier survival analysis showed that there were significant differences in PFS among the three groups. When death was considered a positive event and patients were included in the low- and high-risk groups, there were significant differences in OS between the two groups.ConclusionThe heterogeneity index HI-1 of primary gastric cancer lesions is an independent risk factor for patient prognosis. A nomogram of prognostic prediction models constructed for each independent factor can increase the net clinical benefit and stratify the risk level of patients, providing a reference for guiding individualized patient treatment.
引用
收藏
页码:14535 / 14547
页数:13
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