Evidence map›Paper›PMID 40672100›Full record

ArticleJournal of gastrointestinal oncology2025

Efficacy and safety of transcatheter arterial embolization combined with ablation and regorafenib for unresectable hepatocellular carcinoma patients failing first-line treatment: a real-world study.

Wenfeng Gao, Yiqi Xiong, Tingting Mei, Christine Pocha, Xavier Adhoute, Pierleone Lucatelli, Yonghong Zhang

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
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

7 authors.

Wenfeng Gao *Interventional Therapy Center for Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China.
Yiqi Xiong *Interventional Therapy Center for Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China.
Tingting MeiInterventional Therapy Center for Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China.
Christine PochaAvera Medical Group Hepatology, University of South Dakota, Sioux Falls, SD, USA.
Xavier AdhouteDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille, France.
Pierleone LucatelliVascular and Interventional Radiology Unit, Department of Radiological Oncological and Anatomo-pathological Sciences, Azienda Ospedaliera Universitaria Policlinico Umberto 1, Rome, Italy.
Yonghong ZhangInterventional Therapy Center for Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-1357-7891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Most patients with hepatocellular carcinoma (HCC) have progressed to the intermediate or advanced stage when diagnosed and are ineligible for curative therapies. The currently available therapeutic options, including ablation, radioembolization, transarterial chemoembolization (TACE), and systemic treatment with tyrosine kinase inhibitors (TKIs), provide limited survival benefits. Studies have suggested that the combination treatment may provide better therapeutic outcomes as compared to individual treatments. However, studies of regorafenib in combination with local treatment in patients after failure of first-line treatment are still lacking, and the efficacy of this regimen has not been thoroughly investigated. Therefore, the purpose of our study was to determine the efficacy and safety of TACE combined with regorafenib as second-line therapy in patients with unresectable HCC. Methods: Patients with HCC at Barcelona Clinic Liver Cancer (BCLC) stage B or C who received the combined treatment of TACE, ablation, and regorafenib or regorafenib plus anti-PD-1 immune checkpoint inhibitors (ICIs) in Beijing You'an Hospital between April 2020 to June 2023 were reviewed. The primary endpoint was overall survival (OS), while progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and toxicity were the secondary endpoints. Results: A total of 73 patients were enrolled in our study, including 63 (86.3%) males and 10 (13.7%) females. Among these patients, 16 (21.9%) had portal vein tumor thrombosis (PVTT), and 33 (45.2%) had extrahepatic metastasis. There were 53 (72.6%) patients with multiple tumors and 23 (31.5%) with large tumors (>30 mm). All patients received TACE combined with regorafenib, while 37 (50.7%) additionally received ICIs and 36 (49.3%) did not. The majority (n=61, 83.6%) of patients in our cohort received ablation therapy. There were 22 (30.1%) patients with an alpha fetoprotein (AFP) level >400 U/L. The average follow-up of the cohort was 24.6 months, the median PFS was 7.06 months [95% confidence interval (CI): 4.77-9.36 months], and the median OS was 24.0 months (95% CI: 6.25-41.75 months). According to the modified Response Evaluation Criteria in Solid Tumors, the ORR was 58.9%, and the DCR was 91.8%. No adverse events (AEs) were reported in the 11 patients in the study. The most common any-grade treatment-related AEs were hand-foot syndrome (34.25%), diarrhea (23.29%), and hypertension (21.92%). Grade ≥3 treatment-related AEs occurred in 12.3% of the patients. The most common grade 3 treatment-related AE was hypertension (5.48%). Conclusions: TACE combined with ablation and regorafenib is an effective, safe, and promising second-line treatment option for patients with unresectable HCC after progression from first-line therapy.

Indexed as

ablationHepatocellular carcinoma (HCC)regorafenibsecond-line therapytransarterial chemoembolization (TACE)

Identifiers

PMID40672100
PMCPMC12261014

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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.