Clinical trial · Interventional
Ebastine for Adjuvant Treatment of Tumor Budding-Positive Liver Cancer After Surgery
A Single-Arm Study of Ebastine as Adjuvant Therapy in Patients With Tumor Budding-Positive Hepatocellular Carcinoma After Curative Hepatectomy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study evaluates ebastine, an FAK (focal adhesion kinase) inhibitor, as adjuvant therapy to reduce the risk of recurrence in patients with hepatocellular carcinoma (HCC) who have undergone curative hepatectomy and whose tumors show a histopathological feature known as tumor budding, which is associated with a higher risk of postoperative recurrence. Ebastine is a second-generation antihistamine approved for allergic conditions. Preclinical studies have shown that ebastine also inhibits FAK signaling, a pathway implicated in tumor invasion, epithelial-mesenchymal transition, and recurrence. This study investigates whether administering ebastine after surgery can lower the recurrence risk associated with tumor budding-positive HCC. All enrolled participants will receive ebastine as adjuvant treatment following hepatectomy. The primary endpoint is the 1-year recurrence-free survival (RFS) rate. Secondary endpoints include 2-year RFS, overall survival, and safety. All participants in this study will receive ebastine as adjuvant (after-surgery) treatment. Researchers will monitor whether the cancer stays away for at least one year after surgery (recurrence-free survival), as well as overall survival and any side effects.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepato Cellular Carcinoma | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Ebastine | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Ebastine Adjuvant Treatment Arm
- description
- Participants with tumor budding-positive hepatocellular carcinoma who have undergone curative-intent hepatectomy will receive oral ebastine as adjuvant therapy.
- interventionNames
- Drug: Ebastine
Primary outcomes (1)
- measure
- 1-Year Recurrence-Free Survival (RFS) Rate
- timeFrame
- 1 year after surgery
- description
- Proportion of participants who remain free of tumor recurrence (local, regional, or distant) or death from any cause at 1 year after curative hepatectomy, as assessed by imaging (CT/MRI) per institutional standard follow-up protocol
Secondary outcomes (3)
- measure
- 2-Year Recurrence-Free Survival (RFS) Rate
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age is ≥18 years old, male or female; * Histologically confirmed as hepatocellular carcinoma without metastasis; * Tumor budding is positive * Life expectancy of at least 12 weeks; Exclusion Criteria: * Hepatocellular carcinoma that cannot be surgically resected * Received radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc. before surgery * Pregnant or lactating women * Subjects with other malignant tumors; * Subjects who are considered unsuitable to participate in this cohort study by the investigator; * Subjects who refuse to enroll or do not sign the informed consent form; * Subjects with incomplete medical record information (including gender, age, diagnostic information, imaging (and) or pathological diagnosis results, other demographic data, etc.).
References
Publications (0)
Data not yet available