ArticleEuropean journal of nuclear medicine and molecular imaging2026
Transarterial radioembolisation combined with targeted therapy and immune checkpoint inhibitors in advanced hepatocellular carcinoma with portal vein tumour thrombus: efficacy, safety, and dosimetric analysis.
Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
purposeAdvanced hepatocellular carcinoma (HCC) with portal vein tumour thrombus (PVTT) carries a dismal prognosis. This study evaluated the efficacy and safety of transarterial radioembolisation (TARE) combined with targeted therapy and immune checkpoint inhibitors (ICIs) in patients with HCC and Vp2-Vp4 PVTT, and explored the tumour absorbed dose (TAD) threshold associated with survival benefit.
methodsWe retrospectively analysed 31 patients with HCC and Vp2-Vp4 PVTT treated with this triplet regimen. Tumour responses were assessed per mRECIST and RECIST 1.1. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. The optimal TAD cutoff was identified through dose-threshold exploration and internally validated by bootstrap resampling.
resultsThe objective response rate was 77.4% per mRECIST and 54.8% per RECIST 1.1 (P = 0.023), with a disease control rate of 93.5%. Median PFS and OS were 10.0 months (95% CI, 7.9-NR) and 16.4 months (95% CI, 9.1-NR), respectively. Grade ≥ 3 treatment-related adverse events occurred in 22.6% of patients; no treatment-related death occurred. Exploratory analysis identified TAD ≥ 140 Gy as independently associated with improved PFS after multivariable adjustment (HR = 0.33, 95% CI, 0.11-0.95; P = 0.039), with a concordant trend for OS. Bootstrap validation confirmed robustness.
conclusionTARE combined with targeted therapy and ICIs demonstrates encouraging efficacy with an acceptable safety profile in advanced HCC with Vp2-Vp4 PVTT. TAD ≥ 140 Gy was associated with improved survival, providing a hypothesis-generating basis for personalised dosimetric optimisation in future prospective trials.
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