DEB-TACE Versus DEB-TACE Sequential HAIC for Unresectable BCLC Stage C HCC; A Randomized Controlled Trial

HCC Clinical Trial

Official title:

Drug-eluting Bead Transarterial Chemoembolization and Drug-eluting Bead Transarterial Chemoembolization Sequential Hepatic Artery Chemotherapy Infusion for Unresectable BCLC Stage C HCC: A Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05788835
• Other study ID #: 2023-KY-0081-002
• Status: Recruiting
• Phase: N/A
• Start date: March 7, 2023
• Est. completion date: June 30, 2026

Study information

• Verified date: March 2023
• Source: The First Affiliated Hospital of Zhengzhou University
• Contact: Xuhua Duan, Ph.D.
• Phone: +8613523402912
• Email: xuhuaduan[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized controlled trial to determine the efficacy and safety of DEB-TACE versus DEB-TACE sequential HAIC for unresectable BCLC stage C HCC

Description:

Primary liver cancer is one of the most common malignant tumors in the world. According to the survey results of the BRIDGE study, about 64% of Chinese patients with liver cancer had BCLC stage B and stage C at the first diagnosis, and the vast majority of patients in the middle and advanced stages were no longer suitable for the first choice of surgical resection and should receive comprehensive treatment mainly consisting of local treatment and systemic treatment. TACE is one of the most used treatments for liver cancer. At present, cTACE and DEB-TACE are mainly used. Drug-eluting beads, as new drug-carrying embolisms, have the advantages of loading chemotherapeutic drugs depending on charge and releasing drugs slowly within a certain time to improve local drug concentration. Based on the application of clinical practice, its efficacy has been well confirmed. DEB-TACE results in better tumor response and a similar safety profile than cTACE. However, for HCC at stage C of BCLC, due to the large tumor load and common portal invasion, it is difficult for a single TACE to achieve complete or partial remission, and a complete embolization is likely to increase the risk of serious complications. Hepatic Arterial Infusion Chemotherapy is used to treat hepatic arterial infusion chemotherapy (HCC). HAIC requires chemotherapy drugs to be injected directly into the liver tumor via a percutaneous arterial cannula. HAIC drugs alone stay in the tumor for a short time, will be washed out quickly, and cannot be completely covered for tumors with external hepatic collateral circulation. However, unlike HAIC, DEB-TACE can embolize tumors to nourish arteries, rapidly lead to massive ischemic necrosis of tumors, and significantly prolong the contact time between cancer cells and chemotherapy drugs. In conclusion, the combination of DEB-TACE and HAIC can make up for the respective deficiencies of DEB-TACE and HAIC. And produce enhanced local anti-tumor effect and less AEs, especially in HCC with high tumor load. The combination of DEB-TACE and HAIC has been well tolerated in the treatment of large liver cancer. However, most patients with BCLC stage C HCC have vascular invasion or extrahepatic metastasis, which cannot be treated surgically. Moreover, the progressive involvement of vascular invasion will eventually reduce blood flow and further deteriorate liver function, resulting in impaired liver function and poor prognosis. Therefore, we predict that the DEB-TACE sequential HAIC approach will reduce AEs while achieving good efficacy. Therefore, based on previous studies, this study intended to select patients with unresectable primary liver cancer at stage C of BCLC in a multi-center setting, and prospectively observe the efficacy of DEB-TACE followed by FOLFOX-based HAIC in the treatment of unresectable BCLC stage C patients.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 220
• Est. completion date: June 30, 2026
• Est. primary completion date: June 7, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Patient with unresectable HCC who strictly meet the clinical diagnostic criteria of the Guidelines for Diagnosis and Treatment of Primary Liver Cancer (2022 Edition) or who have been confirmed by histopathology or cytology, There was at least one measurable lesion (according to the requirements of mRECIST 1.1, the spiral CT scan diameter of the measurable lesion was =10mm or the short diameter of enlarged lymph node was =15mm).

2. The sum of the diameter of single or 2-3 tumors =5cm. Tumor stage: Stage C of BCLC.

3. Patient age between 18 and 75,male or female.

4. ECOG 0-1.

5. Expected life span = 3 months.

6. No history of severe comorbidities, such as hypertension, coronary heart disease, and mental illness, and no history of severe allergies.

7. Child-Pugh A-B.

8. HBV DNA<2000 IU/ml.

9. Women of childbearing age must undergo a pregnancy test within 7 days prior to enrollment.

10. Patients sign informed consent, good compliance, cooperate with treatment.

Exclusion Criteria:

1. Imaging examinations were conducted for HCC patients with large liver tumors (=60% of liver volume), or carcinoma thrombus in main portal vein (occupying =50% of vascular diameter), or carcinoma thrombus invading mesenteric vein or inferior vena cava, or significant arteriovenous/venous fistula.

2. Before participating in this study, she had received local treatment such as TACE, external radiotherapy and radioactive particle implantation, and had undergone systemic chemotherapy, oral liver cancer targeting drugs (Sorafenib, Lenfacitinib, Apatinib) and immunotherapy such as PD-1/PD-L1/CDLA-4.

3. Diffuse liver cancer patients.

4. Patients with grade ? or above myocardial ischemia or myocardial infarction, poorly controlled arrhythmias (including QTc interval =450ms for men and 470ms for women.

5. A history of gastrointestinal bleeding within the past 6 months or a definite tendency to gastrointestinal bleeding.

6. Abnormal clotting function, bleeding tendency or receiving thrombolytic or anticoagulant therapy.

7. Patients with central nervous system metastases or known brain metastases. Co-infected patients with HIV; Pregnant or lactating patients. Patients preparing for liver transplantation (other than those with previous liver transplantation.

8. Systemic failure, estimated survival time <3 months.

9. Severe renal dysfunction.

10. The patients could not complete the treatment plan due to various reasons, and lost control within three months after enrollment.

Related Conditions & MeSH terms

• HCC

Intervention

Procedure:
• DEB-TACE and HAIC
Drug-eluting bead transarterial chemoembolization sequential Hepatic Artery Chemotherapy Infusion
• DEB-TACE
Drug-eluting bead transarterial chemoembolization

Locations

Country	Name	City	State
China	Second People's Hospital of Jiaozuo	Jiaozuo
China	Luo He Central Hospital	Luohe	Henan
China	Luo Yang Central Hospital	Luoyang	Henan
China	Deng zhou People's Hospital	Nanyang	Henan
China	Nan Yang Central Hospital	Nanyang	Henan
China	General Hospital of Pingmei Shenma Group	Pingdingshan	Henan
China	First People's Hospital of Shangqiu	Shangqiu	Henan
China	Shangqiu Municipal Hospital	Shangqiu	Henan
China	Xin Yang Central Hospital	Xinyang	Henan
China	The Fifth Affiliated Hospital of Zhengzhou University	Zhengzhou	Henan
China	The First Affiliated Hospital of Zhengzhou University	Zhengzhou	Henan
China	Zhengzhou Central Hospital	Zhengzhou	Henan
China	Zhou Kou Central Hospital	Zhoukou	Henan
China	First People's Hospital of Zhu Madian	Zhumadian	Henan
China	Zhu Ma Dian Central Hospital	Zhumadian	Henan
China	Zhu Madian Traditional Chinese Medicine Hospital	Zhumadian	Henan

Sponsors (1)

Lead Sponsor	Collaborator
Xuhua Duan

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free survival (PFS)	Time from the first DEB-TACE treatment to either radiological progression or death	Time from the first DEB-TACE treatment to either radiological progression or death or up to 36 months
Secondary	Overall survival (OS)	Time from the first DEB-TACE treatment to death from any cause or the end of the study	Time from the first DEB-TACE treatment to death or up to 36 months
Secondary	Objective response rate (ORR)	Proportion of patients with reduction in stable in tumor burden of a predefined amount	1, 3, 6,12 months after the first DEB-TACE treatment, up to death or 36 months, whichever came first
Secondary	Disease control rate (DCR)	Proportion of patients with reduction or keeping in stable in tumor burden of a predefined amount	1, 3, 6,12 months after the first DEB-TACE treatment, up to death or 36 months, whichever came first
Secondary	Time to Progression (TTP)	Time to progression was defined as the period of time from the first on-study DEB-TACE to radiographic disease progression at any site by mRECIST	Time from the first DEB-BACE treatment to either radiological progression up to 36 months