Copyright: ©Author(s) 2026.
World J Gastrointest Oncol. Jun 15, 2026; 18(6): 116250
Published online Jun 15, 2026. doi: 10.4251/wjgo.v18.i6.116250
Published online Jun 15, 2026. doi: 10.4251/wjgo.v18.i6.116250
Table 1 Appraisal of the prognostic model and priorities for future validation
| Domain | Strengths of current model | Limitations and future priorities |
| Evidence synthesis | Large-scale integration of 43 group studies encompassing 5070 patients | Underlying evidence base remains predominantly observational |
| Model variables | Successfully integrates nine readily available clinical parameters (e.g., tumor number, microvascular invasion, Child-Pugh stage, BCLC stage) | Lacks integration of dynamic molecular data and advanced imaging biomarkers |
| Population diversity | Validated externally with real-world clinical data | Skewed toward HBV-endemic regions; requires testing across geographically diverse cohorts and other etiologies (HCV, NASH) |
| Clinical utility | Demonstrates favorable discrimination relative to standard BCLC staging | Requires well-designed interventional studies to definitively test model-guided therapy outcomes |
- Citation: Yang YH. Transcatheter arterial chemoembolization plus lenvatinib toward precision prognostication for unresectable hepatocellular carcinoma. World J Gastrointest Oncol 2026; 18(6): 116250
- URL: https://www.wjgnet.com/1948-5204/full/v18/i6/116250.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v18.i6.116250