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NCT Number: NCT06609876

Donafenib as Adjuvant Therapy Following Ablation for Recurrent HCC

This study intends to evaluate the efficacy and safety of low-dose adjuvant donafenib after thermal ablation for early recurrent HCC within Milan criteria.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Thermal ablation is available as the major curative treatments for early-stage recurrent HCC. Donafenib was inferior to sorafenib in overall survival in untreated advanced hepatocellular carcinoma. No study has evaluated low-dose donafenib as adjuvant therapy after thermal ablation. There needs further investigation to explore the efficacy and safety of the combination treatment. Thus, the investigators carried out this prospective, randomized, open-label, phase II trial study to find out it.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • were aged 18-75 years;
  • had recurrent HCC (RHCC) diagnosed by imaging studies, the first or the second RHCC;
  • RHCC met the Milan criteria, namely single RHCC lesion less than 5 cm in diameter or no more than 3 tumors (each ≤3 cm in diameter);
  • the early RHCC (recurrent time <1 year)
  • patients were unwilling to undergo repeat hepatectomy or liver transplantation;
  • had well-preserved liver function, i.e., Child-Pugh class A or B, and prolonged prothrombin time≤5 s;
  • patients had an Eastern Cooperative Oncology Group performance status score ≤1.
  • Ability to understand the protocol and to agree to and sign a written informed consent document.

Exclusion criteria

  • were under 18 years or over 75 years of age;
  • primary HCC;
  • recurrent HCC beyond Milan criteria;
  • RHCC with metastasis or macrovascular tumor thrombus

Treatment and study plan

Thermal ablation

Procedure

Thermal ablation of tumors

Donafenib

Drug

Donafenib ( 100 mg,bid)

Primary outcomes

  1. Tumor-free survival rate

    Time frame: 24 months

    Progression was defined as progressive disease after thermal ablation by independent radiologic review according to mRECIST or death from any cause

Secondary outcomes

  1. Overall survival (OS)

    Time frame: 36 months

    OS is the length of time from the date of ablation until death from any cause.

  2. Adverse events

    Time frame: 36 months

    Safety will be evaluated according to the NCI CTCAE Version 4.03. All observations pertinent to the safety of the study medication will be recorded on the CRF and included in the final report.

Study contacts

Contact information is provided by the study sponsor or research team.

Feng Duan, Professor

CONTACT

[email protected]

86 13910984586

Qunfang Zhou, MD

CONTACT

[email protected]

86 19868000115

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Collaborators

  • Chinese PLA General Hospital

Registry information

Official study title

Thermal Ablation Combined With Low-dose Donafinib for Early Recurrent Hepatocellular Carcinoma: a Multicenter Prospective Study

Important dates

Study start
2024
Primary completion
2026
Study completion
2028
First posted
Sep 24, 2024
Registry last updated
Dec 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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