NCT06966986

Radiofrequency-responsive Layered Double Hydroxides for Enhanced Arterial Embolization and Thermal Immunotherapy in Hepatocellular Carcinoma

Active, enrolled Last updated 13 May 2025

What this trial tests

trial in Liver Carcinoma in 130 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline

11 September 2024

Primary endpoint
1 August 2025

1 October 2026

Quick facts

Lead sponsor	The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Status	Active, enrolled
Study type	OBSERVATIONAL
Enrollment	130
Start date	11 September 2024
Primary completion	1 August 2025
Estimated completion	1 October 2026
Sites	1 location across China

Conditions studied

• Liver Carcinoma — all drugs for Liver Carcinoma →

Sponsor

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Who can join

18 and older, any sex, with Liver Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Liver cancer is one of the most common malignant tumors and the third leading cause of cancer-related deaths globally. Recent epidemiological studies show that in China, liver cancer ranks fourth in incidence and second in mortality among malignant tumors, posing a serious threat to human health. The common risk factors for liver cancer are chronic inflammatory infections caused by hepatitis B virus (HBV) and hepatitis C virus (HCV), which lead to liver cirrhosis and eventually develop into liver cancer.

The field of liver cancer treatment is characterized by its multidisciplinary approach and the coexistence of various therapeutic methods. Common treatment modalities include liver resection, liver transplantation, ablation therapies, and transcatheter arterial chemoembolization (TACE). Selecting appropriate treatment strategies based on the different stages of liver cancer can maximize therapeutic outcomes.

Although surgical intervention is considered the first-line curative treatment for liver cancer, a significant number of patients are unable to tolerate surgery due to varying degrees of liver cirrhosis and impaired liver function. The limited availability of treatment options results in a relatively low 5-year survival rate of approximately 18% for liver cancer patients. Liver cancer is insidious in onset, highly malignant, and progresses rapidly. Most patients are diagnosed at an advanced stage, having missed the optimal window for surgical resection.

For these patients, interventional therapies based on transcatheter arterial embolization (TAE) have shown excellent antitumor effects and are gradually becoming essential treatment methods for advanced liver cancer. In TAE, embolic agents are injected into the tumor's supplying arteries via a catheter to block the tumor's oxygen and nutrient supply. Currently, embolic agents primarily include liquid embolics (e.g., lipiodol) and solid agents (e.g., microspheres).

However, as a palliative treatment, TAE struggles to completely suppress tumor growth. This limitation arises because these embolic agents are unable to fully and permanently block all tumor vasculature, allowing tumors to establish collateral circulation after the procedure. Additionally, the hypoxic tumor microenvironment created post-procedure stimulates rapid proliferation of liver cancer cells. Consequently, it is critical to develop effective strategies to improve the outcomes of TAE.

Radiofrequency ablation (RFA), a common thermal ablation method for liver cancer in clinical practice, has been widely applied. Leading medical associations, including the U.S. National Comprehensive Cancer Network (NCCN) and the Asia-Pacific Association for the Study of the Liver (APASL), have recognized RFA as a first-line treatment for solitary liver tumors ≤3 cm in size.

During RFA, the central region of the tumor reaches temperatures above 50°C, inducing coagulative necrosis of solid tumors, while the surrounding area, referred to as the transition zone, experiences sublethal heat stress. However, incomplete radiofrequency ablation (iRFA) can occur due to factors such as large tumor size, thermal sink effects of blood vessels, and undetected micro-satellite lesions, leading to rapid recurrence or metastasis of residual tumor tissue.

Studies have reported that RFA can induce specific immune responses by releasing tumor-associated antigens, damage-associated molecular patterns (DAMPs), and pro-inflammatory cytokines from denatured tumor cells. However, the antitumor immune response elicited by RFA is often transient and weak. Moreover, it may trigger a series of immunosuppressive responses, further complicating the overall therapeutic outcome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.