Trial reportFrontiers in immunology2026
Association between gut microbiota characteristics and therapeutic efficacy of multimodal combination therapy in hepatocellular carcinoma with portal vein tumor thrombus: a secondary analysis of a prospective phase II trial.
Trial report in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06040177 (Efficacy and Safety of SBRT Combined With Cardonilizumab and Lenvastinib in the Treatment of Unresectable Hepatocellular Carcinoma With Portal Vein Tumor Thrombus#a Prospective, Multicenter, Single-arm Clinical Study), which is not on this map. Not yet cited in PubMed.
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Efficacy and Safety of SBRT Combined With Cardonilizumab and Lenvastinib in the Treatment of Unresectable Hepatocellular Carcinoma With Portal Vein Tumor Thrombus#a Prospective, Multicenter, Single-arm Clinical Study
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16 authors.
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Abstract
Background: Hepatocellular carcinoma (HCC) with portal vein tumor thrombus (PVTT) carries a poor prognosis. Although SBRT combined with cadonilimab and lenvatinib has shown encouraging antitumor activity in a prior prospective phase II trial, marked interpatient heterogeneity remains. Gut microbiota may influence antitumor immunity and could help identify patients more or less likely to benefit from this regimen. Objective: To characterize baseline and longitudinal gut microbiota features in treatment-naïve HCC patients with PVTT receiving SBRT plus cadonilimab and lenvatinib, and to explore microbial signatures associated with therapeutic response. Methods: This is a complementary exploratory study nested within the aforementioned phase II trial. In this prospective multicenter exploratory cohort, 23 patients from the parent trial provided 46 paired fecal samples collected before treatment (Phase A) and after 3 cycles of cadonilimab (Phase B). Patients were categorized by best mRECIST response as responders (group C, CR/PR; n = 10) or non-responders (group D, SD/PD; n = 13), consistent with the parent trial's grouping strategy. 16S rRNA amplicon sequencing and downstream bioinformatic analyses were performed to assess microbial diversity, differential taxa, predicted KEGG functional profiles, and exploratory discriminatory performance. Results: A total of 1,410,203 high-quality non-chimeric reads were retained and rarefied to 5,459 reads per sample. Baseline α-diversity indices were largely comparable between groups, although Faith's phylogenetic diversity was higher in responders (P = 0.0178). β-diversity did not show clear between-group separation at baseline or marked restructuring after treatment. Genus-level DESeq2 analysis identified 7 baseline differential genera. Conclusions: In HCC patients with PVTT treated with SBRT plus cadonilimab and lenvatinib, the overall gut microbiota architecture remained relatively stable, whereas selected baseline genus-level features were associated with therapeutic response. Clinical Trial Registration: ClinicalTrials.gov, identifier NCT06040177.
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