A Randomized Controlled Trial Evaluating Different Doses of Oral Zinc Supplementation in Combination With Targeted Immunotherapy for Unresectable or Advanced Hepatocellular Carcinoma

NCT07793695 | Not Yet Recruiting Phase 2

• 1 other identifier: 2026KY1085
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

This study will look at whether adding daily oral zinc supplements to targeted therapy plus immunotherapy may help people with unresectable or advanced hepatocellular carcinoma, a common type of liver cancer. About 60 participants will take part in this study. Participants will be randomly assigned to one of three groups. One group will receive targeted therapy plus immunotherapy without extra zinc. The other two groups will receive the same type of cancer treatment together with either 20 mg or 30 mg of elemental zinc each day. The main goal is to compare how many participants have their tumors shrink or disappear by Week 16. Researchers will also look at tumor response at earlier time points, how long the cancer remains under control, overall survival, and treatment safety. Blood tests will be used to measure zinc and copper levels during the study. Researchers will also study changes in immune cells, including T cells, to better understand whether zinc supplementation may affect the body's immune response to cancer treatment. This study is designed to explore whether oral zinc supplementation is safe and may improve the effects of targeted therapy plus immunotherapy. The results may help determine which zinc dose should be studied in larger clinical trials.

Conditions

Hepatocellular Carcinoma

Keywords

Hepatocellular carcinoma; Targeted therapy plus immunotherapy; Zinc supplementation; Objective response rate

Outcome Measures

Primary Outcomes (1)

• Objective Response Rate at Week 16

  Proportion of participants achieving complete response (CR) or partial response (PR) at Week 16 according to RECIST v1.1. ORR = (CR + PR) / total number of participants in the analysis set × 100%.

  At Week 16 after initiation of study treatment

Secondary Outcomes (11)

• Objective Response Rate (ORR) at Week 8

  At Week 8 after initiation of study treatment.

• Objective Response Rate (ORR) by mRECIST

  At Weeks 8 and 16 after initiation of study treatment.

• Disease Control Rate

  At Weeks 8 and 16 after initiation of study treatment.

• Progression-Free Survival

  From enrollment until disease progression or death, whichever occurs first.

• Overall Survival

  From enrollment until death from any cause.

Study Arms (3)

Control Group

ACTIVE COMPARATOR

Participants will receive standard-of-care targeted therapy plus immunotherapy without additional zinc supplementation.

Drug: Standard-of-care targeted therapy plus immunotherapy

Zinc 20 mg/day Group

EXPERIMENTAL

Participants will receive standard-of-care targeted therapy plus immunotherapy together with oral elemental zinc supplementation at a dose of 20 mg/day.

Drug: Oral elemental zinc supplementation, 20 mg/day; Drug: Standard-of-care targeted therapy plus immunotherapy

Zinc 30 mg/day Group

EXPERIMENTAL

Participants will receive standard-of-care targeted therapy plus immunotherapy together with oral elemental zinc supplementation at a dose of 30 mg/day.

Drug: Oral elemental zinc supplementation, 30 mg/day; Drug: Standard-of-care targeted therapy plus immunotherapy

Interventions

Oral elemental zinc supplementation, 20 mg/day DRUG

Participants will receive oral elemental zinc supplementation at a dose of 20 mg/day. Zinc gluconate tablets will be administered orally, 1 tablet twice daily after meals.

Zinc 20 mg/day Group

Oral elemental zinc supplementation, 30 mg/day DRUG

Participants will receive oral elemental zinc supplementation at a dose of 30 mg/day. Zinc gluconate tablets will be administered orally, 1 tablet three times daily after meals.

Zinc 30 mg/day Group

Standard-of-care targeted therapy plus immunotherapy DRUG

The background targeted therapy plus immunotherapy regimen will be determined by the investigator based on the participant's clinical condition, applicable treatment guidelines, prescribing information, and routine clinical practice at the study center. Permitted regimens include sintilimab plus bevacizumab or a bevacizumab biosimilar, tislelizumab plus lenvatinib, and atezolizumab plus bevacizumab. The background treatment regimen should remain unchanged during the study whenever clinically feasible. If treatment modification is required because of toxicity, intolerance, disease progression, drug availability, or other clinical considerations, the reason for and details of the modification will be documented in the case report form (CRF).

Control Group; Zinc 20 mg/day Group; Zinc 30 mg/day Group

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female participants aged 18-75 years who are able to understand the study and voluntarily provide written informed consent.
• Histologically or cytologically confirmed hepatocellular carcinoma (HCC) that is unresectable, recurrent, or metastatic.
• Estimated life expectancy of more than 3 months.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
• At least one measurable lesion according to RECIST v1.1. The lesion must not have received prior local therapy; if previously treated locally, there must be documented disease progression, defined as an increase of ≥20% in the sum of diameters from the post-treatment nadir with an absolute increase of ≥5 mm, or the appearance of a new lesion meeting RECIST v1.1 measurability criteria.
• Child-Pugh class A, score 5-6, with no clinically significant ascites, hepatic encephalopathy, or recent hepatic decompensation.
• Barcelona Clinic Liver Cancer (BCLC) stage B that is unsuitable for or no longer suitable for local treatment, or BCLC stage C.
• No prior systemic antitumor therapy for unresectable, recurrent, or metastatic HCC, including immune checkpoint inhibitors, anti-VEGF/VEGFR-targeted therapy, tyrosine kinase inhibitors (TKIs), systemic chemotherapy, or other systemic anticancer agents. Prior local treatments, including surgery, ablation, transarterial chemoembolization (TACE), hepatic arterial infusion chemotherapy (HAIC), or radiotherapy, are permitted provided that treatment was completed ≥4 weeks before enrollment and related toxicities have recovered to Grade ≤1 or are considered by the investigator not to interfere with study participation.
• Planned treatment with targeted therapy plus immunotherapy in accordance with applicable treatment guidelines and clinical practice, with the specific background antitumor regimen determined by the investigator before enrollment. The background regimen should not be changed arbitrarily during the study.
• If the background treatment regimen includes bevacizumab or another anti-VEGF monoclonal antibody, the participant must undergo upper gastrointestinal endoscopy during screening or have an evaluable endoscopic examination performed within 6 months before screening. Participants with esophagogastric varices requiring treatment may be enrolled only after appropriate management and when the investigator considers the bleeding risk to be adequately controlled.
• Baseline testing for serum zinc, serum copper, and ceruloplasmin must be completed.
• Adequate major organ function to receive targeted therapy plus immunotherapy, including:
• Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L
• Platelet count ≥75 × 10⁹/L
• Hemoglobin ≥90 g/L

You may not qualify if:

• Primary liver cancer histology other than predominant HCC, such as intrahepatic cholangiocarcinoma or combined hepatocellular-cholangiocarcinoma, or the presence of another active malignancy requiring systemic treatment.
• Prior systemic antitumor therapy for unresectable, recurrent, or metastatic HCC. Participants who have previously received PD-1, PD-L1, or CTLA-4 inhibitors, or systemic anti-VEGF/VEGFR therapy, will be excluded.
• Active autoimmune disease, a history of severe immune-related adverse events, or requirement for systemic immunosuppressive therapy within 14 days before screening.
• Clinically significant ascites, such as ascites requiring repeated paracentesis, albumin infusion, or showing recent rapid worsening; current or previous hepatic encephalopathy, hepatorenal syndrome, or other clear evidence of hepatic decompensation.
• Confirmed copper deficiency, Wilson disease, Menkes disease, or other clinically significant disorders of copper metabolism; participants currently receiving zinc salts for the treatment of Wilson disease will be excluded.
• Use of zinc-containing supplements, multivitamin/mineral preparations, zinc-containing denture adhesives, or other supplements that may significantly affect zinc or copper levels within 14-28 days before screening, if such products cannot be discontinued.
• Conditions that may significantly affect oral drug absorption or adherence, including persistent vomiting, severe diarrhea, short bowel syndrome, active inflammatory bowel disease, gastrointestinal obstruction, severe dysphagia, or any condition that, in the investigator's judgment, would prevent regular oral administration of the study medication.
• Known severe hypersensitivity to zinc preparations or any drug used in the background targeted therapy plus immunotherapy regimen.
• Active severe infection. Participants with HBV DNA positivity accompanied by elevated viral load and ALT and/or AST above the upper limit of normal, with evidence of active hepatic inflammation, will be excluded. Participants who are HBsAg-positive but HBV DNA-negative with normal liver biochemistry will not be excluded solely on the basis of HBV carrier status.
• Untreated or inadequately treated esophagogastric varices, or other portal hypertension-related lesions considered by the investigator to confer a high bleeding risk; gastrointestinal bleeding, hemoptysis, intracranial hemorrhage, or any other Grade ≥3 bleeding event within 6 months before screening.
• Uncontrolled hypertension, severe cardiovascular or cerebrovascular disease, recent myocardial infarction, stroke, or pulmonary embolism, severe arrhythmia, NYHA class III-IV heart failure, or any condition that, in the investigator's judgment, would preclude safe treatment with anti-VEGF therapy or a TKI.
• Major surgery within 28 days before screening, unhealed open wounds, active peptic ulcer disease, high risk of gastrointestinal perforation or fistula, or any condition that may adversely affect the safety of bevacizumab or other anti-VEGF therapy.
• Uncontrolled central nervous system metastases or leptomeningeal metastases, or symptomatic CNS disease.
• Pregnancy, breastfeeding, or a positive pregnancy test during screening.
• Planned use during the study of any antitumor treatment, investigational drug, or nutritional intervention outside the protocol that could interfere with assessment of antitumor efficacy.

Sponsors & Collaborators

• Anhui Provincial Hospital: lead

Study Sites (1)

The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)

Hefei, Anhui, 230001, China

Location

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Interventions

Immunotherapy

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)

Immunomodulation; Biological Therapy; Therapeutics

Study Officials

• Lianxin Liu

  The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Yao Liu, Dr

CONTACT

0551-62284121; liuyao66@ustc.edu.cn

Hua Lu, MD

CONTACT

0551-62283822

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER GOV
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 26, 2026
• First Posted: August 28, 2026
• Study Start (Estimated): September 1, 2026
• Primary Completion (Estimated): August 1, 2027
• Study Completion (Estimated): December 31, 2027
• Last Updated: August 28, 2026

Record last verified: 2026-08

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)