Identification of gastroenteropancreatic neuroendocrine tumor patients with high liver tumor burden based on clinicopathological features

基于临床病理特征识别肝脏肿瘤负荷高的胃肠胰神经内分泌肿瘤患者

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Abstract

BACKGROUND: Metastatic liver tumor burden (LTB) is a prognostic factor affecting the survival of gastroenteropancreatic neuroendocrine tumors (GEP-NETs), but evaluation of the LTB usually depends on radiologic and functional imaging. This study aimed to develop a clinical model based on easily accessible clinicopathological markers to predict LTB level in GEP-NET patients. METHODS: LTB was quantified based on (68)Ga-DOTANOC PET/CT scan. The optimal cut-off value for high and low-LTB was determined based on our previous study. Serum levels of liver enzymes and tumor biomarkers were obtained within one week before PET/CT scan. The whole dataset was divided into training set and validation set. LASSO regression method was used to select predictors, and multivariate logistic regression was used to develop a clinical model which was further visualized by constructing a nomogram. Area under the curve (AUC) was applied to assess the accuracy of the constructed model. RESULTS: We retrospectively enrolled 200 patients with well-differentiated GEP-NETs. Ki-67 index, GGT (gamma-glutamyltransferase), LDH (lactate dehydrogenase), and NSE (neuron-specific enolase) were selected through the LASSO regression method, and a nomogram was built based on these variables. The predictive model yielded an AUC of 0.785 (95% CI, [0.708–0.862]) in the training set, and 0.783 (95% CI, [0.644–0.923]) in the validation set. Additionally, with the optimal cut-off values based on the nomogram total points, patients were categorized as LTB(high) (total points ≥ 26.2) and LTB(low) (total points < 26.2) groups presenting significantly different OS. CONCLUSION: A clinically applicable nomogram incorporating four clinicopathological characteristics was constructed to predict GEP-NET patients with high-LTB. The nomogram may help clinicians identify patients with high-LTB and take optimal treatment measures to improve prognosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-025-14535-9.

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