Two-nodule hepatocellular carcinoma without satellites has outcomes similar to solitary HCC
Retrospective analysis of 153 patients with multifocal HCC found that synchronous two-nodule HCC without satellite lesions showed no significant difference in overall or recurrence-free survival compared to solitary HCC. In contrast, satellite-nodule HCC had significantly worse outcomes. Microvascular invasion and satellite nodules, but not two-nodule multifocality, were independent adverse prognostic factors. A simplified morphology-based stratification may better reflect clinical outcomes than traditional multicentric versus metastasis classification.
The original study
Synchronous two-nodule hepatocellular carcinoma without satellite nodules is associated with better survival outcomes compared with satellite-nodule hepatocellular carcinoma.
- Authors
- Wu YH, Tseng YF, Yang YJ, Hung WT, Jeng YM
- Journal
- Journal of clinical pathology
- PMID
- 41708315
Original abstract
AIMS: Multifocal hepatocellular carcinoma (HCC) is traditionally classified as multicentric occurrence (MO) or intrahepatic metastasis, a distinction that is difficult to apply in routine practice and not reflected in current staging systems. We aimed to assess the prognostic significance of different multifocal HCC patterns using simple, clinically applicable criteria. METHODS: We retrospectively analysed 153 patients with synchronous multifocal HCC who underwent surgical resection, including cases with two discrete nodules, more than two nodules and satellite nodules. 76 patients with solitary HCC served as controls. Histological classification based on Liver Cancer Study Group of Japan criteria was supplemented with TERT promoter mutation analysis in selected cases. Overall survival (OS) and recurrence-free survival (RFS) were evaluated using Kaplan-Meier and Cox regression analyses. RESULTS: Histologic criteria alone failed to classify a substantial proportion of two-nodule HCCs. Although TERT promoter analysis allowed partial reclassification, patients with undetermined two-nodule HCC had survival outcomes comparable to those classified as MO. In contrast, HCCs with satellite nodules showed significantly poorer OS and RFS. Multivariate analysis identified microvascular invasion and the presence of satellite nodules-but not two-nodule multifocality-as independent adverse prognostic factors. Notably, patients with two discrete nodules without satellite lesions did not show a statistically significant difference in OS or RFS compared with those with solitary HCC. CONCLUSIONS: Synchronous two-nodule HCC without satellite nodules represents a prognostically favourable subgroup distinct from satellite-nodule HCC. A simplified morphology-based stratification may better reflect clinical outcomes in multifocal HCC.