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Updated: Sep 19, 2026

Isolated Hepatic Perfusion as a Treatment for Liver Metastases of Uveal Melanoma
Published on: January 25, 2015
Association of week-2 Contrast-Enhanced Ultrasound Perfusion Changes with Response to Lenvatinib Plus PD-1 Inhibitors
Hang Su1, Yang Gao2, Song Zhang3
1Department of Ultrasound, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.
Background:
To explore whether early contrast-enhanced ultrasound (CEUS)-derived tumor perfusion changes were associated with subsequent response to Lenvatinib plus PD-1 inhibitors in unresectable hepatocellular carcinoma (HCC).
Methods:
This study included 74 patients with unresectable HCC treated with Lenvatinib plus PD-1 inhibitors in routine clinical practice retrospectively. Baseline and early on-treatment CEUS examinations at approximately 2 weeks after treatment initiation were analyzed to quantify tumor perfusion parameters. Objective response rate (ORR), disease control rate (DCR), duration of response (DoR), progression-free survival (PFS) and overall survival (OS) were study endpoints. Associations between CEUS findings and treatment outcomes were analyzed.
Results:
ORR of Lenvatinib plus PD-1 inhibitors among 74 patients with HCC was 33.8% (95% CI: 23.2-45.7%) and DCR was 73.0% (95% CI: 61.4-82.6%). Median DoR among the 25 responders was 8.7 months (95% CI: 7.39-10.01 months). After a median follow-up duration of 21.1 months, median PFS was 6.9 months (95% CI: 4.33-9.47 months) and median OS was 21.3 months (95% CI: 14.70-27.90 months). CEUS perfusion analysis showed that baseline tumor enhancement did not significantly differ between eventual responders and non-responders. In contrast, week-2 CEUS-derived perfusion changes, particularly percentage reduction in AUC, were associated with subsequent radiologic response. Using an exploratory cutoff of ≥35% AUC reduction, patients above this threshold showed longer PFS and OS than those below the threshold. These associations remained exploratory because the threshold was derived within a limited retrospective cohort. Treatment was generally well tolerated, no unexpected adverse events occurred, and there were no treatment-related deaths in this cohort.
Conclusion:
In this single-center retrospective exploratory cohort, week-2 CEUS-derived AUC reduction was associated with subsequent radiological response and survival outcomes in patients with unresectable HCC receiving Lenvatinib plus PD-1 inhibitors. These findings should be interpreted as hypothesis-generating and require prospective validation before CEUS-based perfusion changes can be used for clinical decision-making.
