Icaritin Soft Capsule Combined With Lenvatinib and TACE for the Treatment of Hepatocellular Carcinoma

NCT05903456 | Unknown Phase 2

• 1 other identifier: IRB-2022-802
• Study Type: interventional
• Target: 20
• Locations: 0 countries
• Sites: N/A

Brief Summary

The investigators design a phase II clinical study to explore the efficacy and safety of Transarterial Chemoembolization (TACE) + Lenvatinib + Icaritin soft capsules in patients with Unresectable, non-metastatic hepatocellular carcinoma and to analyze potential biomarkers of therapeutic response.

Conditions

Hepatocellular Carcinoma

Keywords

Hepatocellular carcinoma; Icaritin soft capsules;TACE; lenvatinib

Outcome Measures

Primary Outcomes (1)

• Objective Response Rate

  It was defined as the percentage of patients with complete response (CR) and partial response (PR) in all patients, and the treatment response was based on the modified response evaluation criteria in solid tumors (recist1.1)

  48 weeks

Secondary Outcomes (5)

• progression-free survival

  96 weeks

• Overall Survival

  96 weeks

• Disease Control Rate

  48 weeks

• Duration of Response

  up to 48 weeks

• adverse event

  96 weekes

Study Arms (1)

TACE +lenvatinib+Icaritin soft capsules

EXPERIMENTAL

Trial drug Lenvatinib, 8mg (2 tablets for patients weighing less than 60kg), or 12mg (3 tablets for patients weighing more than 60kg), once daily. Icariin Soft Capsules 1200 mg/d (6 tablets in two doses) should be swallowed with warm water within 30 minutes after meal. Take lenvatinib and Icaritin soft capsules 3 to 5 days after TACE. Until the disease progresses or the patient becomes intolerant.

Procedure: TACE（transcatheter arterial chemoembolization）; Drug: lenvatinib; Drug: Icaritin soft capsules

Interventions

TACE（transcatheter arterial chemoembolization） PROCEDURE

TACE treatment is strictly in accordance with the Chinese guidelines for clinical practice of transcatheter arterial chemoembolization (TACE) for hepatocellular carcinoma (2018 Edition). The patients with HCC were selected according to the inclusion criteria (referring to the conditions of the subjects). The subjects who met the inclusion criteria could enter the study after they signed the informed consent. 4-6 weeks after the first TACE treatment, the resectability criteria were evaluated. If not, the next cycle of TACE treatment was carried out. The general principle is to reduce the number of interventional treatment and extend the interval of interventional operation as far as possible under the condition of controlling the tumor and the survival of patients with tumor.

TACE +lenvatinib+Icaritin soft capsules

lenvatinib DRUG

Ronvastinib is an orally administered multi-receptor tyrosine kinase (RTK) inhibitor that selectively inhibits the kinase activity of vascular endothelial growth factor (VEGF) receptors, such as VEGF-1, VEGF-2, and VEGF-3, in addition to inhibiting other pro-angiogenic and oncogenic signaling pathways associated with tumor proliferation ，has been approved as a first-line treatment for liver cancer

Also known as: target drug

TACE +lenvatinib+Icaritin soft capsules

Icaritin soft capsules DRUG

Icaritin soft capsule is a flavonoid compound extracted from traditional Chinese medicinal materials. It is a new type of small molecule immunomodulator. It is a 1.2 class of innovative Chinese medicine with global independent intellectual property rights. By inhibiting inflammatory signaling pathway and reducing the release of inflammatory factors, the immune microenvironment can be regulated to play an anti-tumor role. At present, it has been approved for first-line treatment of advanced liver cancer, with good efficacy and safety.

Also known as: Small molecule immunomodulator

TACE +lenvatinib+Icaritin soft capsules

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Between the ages of 18 and 80;
• Patients with histological/cytological confirmed hepatocellular carcinoma.
• HCC patients eligible for China liver cancer staging (CNLC) Stage IIIa, which cannot be resectable, are not suitable for radical treatment.
• According to the RECIST v1.1 standard, there must be at least one measurable lesion on the upper abdominal enhanced CT or MRI.
• Child-Pugh grade A or B;
• ECOG physical condition score is 0 or 1;
• Suitable for the indications of TACE surgery and chemotherapy drugs prescribed in advance by the research center, without any contraindications.
• Regular antiviral therapy should be given if HBV or HCV infection is present.
• Life expectancy is more than 3 months
• Able to swallow and absorb oral tablets;
• Appropriate organ function with the following laboratory test values obtained within 7 days prior to therapeutic use:
• (hemoglobin value ≥80g/L, neutrophil count ≥2.5×109/L, platelet count ≥75×109/L, serum total bilirubin ≤2× upper limit of normal (UNL), aspartic transferase ≤2×UNL, alanine transferase ≤3×UNL, serum creatinine ≤1.5×UNL)
• Manageable blood pressure
• Women of childbearing age must already be using reliable contraception or have had a negative pregnancy test (serum or urine) within 7 days prior to enrollment and be willing to use an effective method of contraception during the trial period and within 2 months after the last drug administration. Male subjects whose partners are women of childbearing age should use effective methods of contraception during the trial period and within 2 months after the last dose;
• The subjects voluntarily joined the study, signed the informed consent, had good compliance, and cooperated with follow-up.

You may not qualify if:

• Formation of portal vein main cancer thrombus or extensive cancer thrombus.
• HCC was treated with local treatment of existing lesions (e.g., TACE, ablation, particle, TARE, hepatic arterial infusion chemotherapy, or radiotherapy).
• Patients who have previously received targeted or immunoreactive anti-tumor therapy for HCC and chemotherapy need to be desensitized for more than one month.
• Subjects were unable to perform enhanced CT or MRI scans of the liver.
• Have a history of liver transplantation or are currently candidates for liver transplantation.
• Patients at high risk for esophageal or gastric variceal bleeding or unproven severe variceal bleeding within the last 3 months.
• Have bleeding or thrombotic disease or are receiving thrombolytic therapy
• Study clinically significant hemoptysis or tumor hemorrhage of any cause within 2 weeks prior to initial administration of the intervention.
• Study of significant cardiovascular impairment in the 12 months prior to initial administration, such as a history of congestive heart failure above NYHA Grade II (Appendix 12), unstable angina, myocardial infarction or cerebrovascular stroke, or arrhythmias associated with hemodynamic instability.
• There was clinically significant ascites on physical examination, which could not be controlled by drugs.
• Known to be allergic to any component of icartin soft capsules and lenvatinib preparation.
• Pregnant or lactating female patients.
• Other conditions in which participation in the study is not appropriate according to the investigator's judgment.

Sponsors & Collaborators

• Zhejiang Cancer Hospital: lead

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Interventions

lenvatinib; Drug Delivery Systems

Condition Hierarchy (Ancestors)

Adenocarcinoma; Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Liver Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Digestive System Diseases; Liver Diseases

Intervention Hierarchy (Ancestors)

Drug Therapy; Therapeutics

Central Study Contacts

guoliang Shao, doctor

CONTACT

13958183472; shaogl@zjcc.org.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Masking Details: NO masking
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Chief Physician

Study Record Dates

• First Submitted: May 19, 2023
• First Posted: June 15, 2023
• Study Start: July 1, 2023
• Primary Completion: May 1, 2025
• Study Completion: December 1, 2025
• Last Updated: June 15, 2023

Record last verified: 2023-06

Data Sharing

• IPD Sharing: Will not share