Evidence map›Paper›PMID 42682622›Full record

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.

Xinwen Liang, Ye Li, Minhui Liang, Zhiming Zeng, Kai Hu, Lihua Yang, Hui Yan, Muyun Li, Jie Zeng, Jing Tang and 6 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06040177 phase1 / phase2unknown statusnot on this map

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

TypeinterventionalSponsorFirst Affiliated Hospital of Guangxi Medical UniversityRan2023 to 2025Enrolled30ConditionsHepatocellular Carcinoma Non-resectable, Portal Vein Tumor Thrombus, Immune Checkpoint InhibitorsArmsCadonilimab, Stereotactic radiotherapy, Renvatinib
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Xinwen Liang *First Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Ye Li *Department of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Minhui Liang *First Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Zhiming ZengDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Kai HuDepartment of Radiation Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Lihua YangDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Hui YanFirst Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Muyun LiFirst Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Jie ZengDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Jing TangDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Yufeng LvDepartment of Oncology, Foresea Life Insurance Guangxi Hospital, Nanning, Guangxi, China.
Li LiangDepartment of Oncology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Jiali MengDepartment of Radiation Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Huabin SuDepartment of Science and Education, Jiangbin Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Jie MaDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Ning MoDepartment of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Carcinoma, HepatocellularGastrointestinal MicrobiomeLiver NeoplasmsPortal VeinVenous ThrombosisAgedAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleHumansMaleMiddle AgedPhenylurea CompoundsProspective StudiesQuinolinesAntibodies, Monoclonal, HumanizedlenvatinibPhenylurea CompoundsQuinolinescadonilimabgut microbiotahepatocellular carcinomaimmunotherapylenvatinibportal vein tumor thrombusstereotactic body radiotherapy

Identifiers

PMID42682622
PMCPMC13529949

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.