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Model containing sarcopenia and visceral adiposity can better predict the prognosis of hepatocellular carcinoma: a multicenter study

AIM: This study aimed to explore whether the addition of sarcopenia and visceral adiposity could improve the accuracy of model predicting progression-free survival (PFS) in hepatocellular carcinoma (HCC). METHODS: In total, 394 patients with HCC from five hospitals were divided into the training and...

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Detalles Bibliográficos
Autores principales: Liu, Yao, Fu, Sirui, Yu, Xiangrong, Zhang, Jinxiong, Zhu, Siyu, Yang, Yang, Huang, Jianwen, Luo, Hanlin, Tang, Kai, Zheng, Youbing, Zhao, Yujie, Chen, Xiaoqiong, Zhan, Meixiao, He, Xiaofeng, Li, Qiyang, Duan, Chongyang, Chen, Yuan, Lu, Ligong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568831/
https://www.ncbi.nlm.nih.gov/pubmed/37828461
http://dx.doi.org/10.1186/s12885-023-11357-5
Descripción
Sumario:AIM: This study aimed to explore whether the addition of sarcopenia and visceral adiposity could improve the accuracy of model predicting progression-free survival (PFS) in hepatocellular carcinoma (HCC). METHODS: In total, 394 patients with HCC from five hospitals were divided into the training and external validation datasets. Patients were initially treated by liver resection or transarterial chemoembolization. We evaluated adipose and skeletal muscle using preoperative computed tomography imaging and then constructed three predictive models, including metabolic (Model(MA)), clinical–imaging (Model(CI)), and combined (Model(MA−CI)) models. Their discrimination, calibration, and decision curves were compared, to identify the best model. Nomogram and subgroup analysis was performed for the best model. RESULTS: Model(MA−CI) containing sarcopenia and visceral adiposity had good discrimination and calibrations (integrate area under the curve for PFS was 0.708 in the training dataset and 0.706 in the validation dataset). Model(MA−CI) had better accuracy than Model(CI) and Model(MA). The performance of Model(MA−CI) was not affected by treatments or disease stages. The high-risk subgroup (scored > 198) had a significantly shorter PFS (p < 0.001) and poorer OS (p < 0.001). CONCLUSIONS: The addition of sarcopenia and visceral adiposity improved accuracy in predicting PFS in HCC, which may provide additional insights in prognosis for HCC in subsequent studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11357-5.