Lasso-Cox interpretable model of AFP-negative hepatocellular carcinoma

被引:0
|
作者
Li, Han [1 ]
Zhou, Chengyuan [1 ]
Wang, Chenjie [1 ]
Li, Bo [2 ]
Song, Yanqiong [3 ]
Yang, Bo [1 ]
Zhang, Yan [4 ]
Li, Xueting [5 ]
Rao, Mingyue [1 ]
Zhang, Jianwen [1 ]
Su, Ke [1 ,6 ]
He, Kun [7 ]
Han, Yunwei [1 ]
机构
[1] Southwest Med Univ, Dept Oncol, Affiliated Hosp, Taiping St, Luzhou 646000, Sichuan, Peoples R China
[2] Southwest Med Univ, Dept Gen Surg Hepatobiliary Surg, Affiliated Hosp, Luzhou 646000, Peoples R China
[3] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med, Chengdu, Peoples R China
[4] Southwest Med Univ, Dept Oncol, Affiliated Hosp Tradit Chinese Med, Luzhou 646000, Peoples R China
[5] 363 Hosp, Dept Oncol, Chengdu, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, Natl Clin Res Ctr Canc, Dept Radiat Oncol,Canc Hosp, Beijing, Peoples R China
[7] Southwest Med Univ, Clin Med Coll, Luzhou 646000, Peoples R China
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2025年 / 27卷 / 01期
关键词
Machine learning; Hepatocellular carcinoma; AFP; Interpretable; ALPHA-FETOPROTEIN; PROGNOSIS; EXPRESSION; NOMOGRAM; SERUM;
D O I
10.1007/s12094-024-03588-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundIn AFP-negative hepatocellular carcinoma patients, markers for predicting tumor progression or prognosis are limited. Therefore, our objective is to establish an optimal predicet model for this subset of patients, utilizing interpretable methods to enhance the accuracy of HCC prognosis prediction.MethodsWe recruited a total of 508 AFP-negative HCC patients in this study, modeling with randomly divided training set and validated with validation set. At the same time, 86 patients treated in different time periods were used as internal validation. After comparing the cox model with the random forest model based on Lasso regression, we have chosen the former to build our model. This model has been interpreted with SHAP values and validated using ROC, DCA. Additionally, we have reconfirmed the model's effectiveness by employing an internal validation set of independent periods. Subsequently, we have established a risk stratification system.ResultsThe AUC values of the Lasso-Cox model at 1, 2, and 3 years were 0.807, 0.846, and 0.803, and the AUC values of the Lasso-RSF model at 1, 2, and 3 years were 0.783, 0.829, and 0.776. Lasso-Cox model was finally used to predict the prognosis of AFP-negative HCC patients in this study. And BCLC stage, gamma-glutamyl transferase (GGT), diameter of tumor, lung metastases (LM), albumin (ALB), alkaline phosphatase (ALP), and the number of tumors were included in the model. The validation set and the separate internal validation set both indicate that the model is stable and accurate. Using risk factors to establish risk stratification, we observed that the survival time of the low-risk group, the middle-risk group, and the high-risk group decreased gradually, with significant differences among the three groups.ConclusionThe Lasso-Cox model based on AFP-negative HCC showed good predictive performance for liver cancer. SHAP explained the model for further clinical application.
引用
收藏
页码:309 / 318
页数:10
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