Combining HAIC with Donafenib and Sintilimab for Liver Cancer Treatment

HAIC Combined with Donafenib and Sintilimab As Perioperative Treatment for Resectable Hepatocellular Carcinoma Patients At High Risk of Recurrence: a Prospective, Multicenter, Randomized Phase II Study

This study is testing if a new combination of chemotherapy and medications can help people with liver cancer who are at high risk of their cancer coming back after surgery.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 165 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: Fudan University (Academic / other)
• Drugs / interventions: sintilimab
• Locations: 3 sites (Fuzhou, Fujian and 2 other locations)
• Trial ID: NCT06812039 on ClinicalTrials.gov

What this trial studies

This study evaluates the effectiveness and safety of a perioperative treatment regimen combining hepatic arterial infusion chemotherapy (HAIC) with donafenib and sintilimab in patients with resectable hepatocellular carcinoma (HCC) who are at high risk of recurrence. Participants will be divided into three groups: one receiving the combination therapy, another receiving only donafenib and sintilimab, and a control group undergoing direct surgery. The goal is to determine if the combination therapy can improve outcomes compared to surgery alone.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 to 75 with histologically confirmed untreated hepatocellular carcinoma that is resectable and meets specific tumor burden criteria.

Not a fit: Patients with unresectable HCC or those with severe liver dysfunction (Child-Pugh class B or C) may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could significantly reduce the risk of recurrence in patients with hepatocellular carcinoma after surgery.

How similar studies have performed: Other studies have shown promising results with similar combination therapies in treating hepatocellular carcinoma, indicating potential for success in this approach.

Eligibility criteria

Inclusion Criteria:

* Voluntary enrollment with written informed consent obtained
* Age 18 to 75 years (inclusive), regardless of gender
* Histologically or pathologically confirmed previously untreated hepatocellular carcinoma (HCC) or clinically diagnosed previously untreated HCC according to the AASLD guidelines.
* Initial resectable status as assessed by the investigator (expected to achieve R0 resection, sufficient liver remnant volume, and Child-Pugh class A, as per the "Chinese Expert Consensus on Neoadjuvant Therapy for Liver Cancer (2023 Edition)").
* At least one measurable lesion according to mRECIST criteria.
* Tumor burden meets one of the following conditions:

  1. A single tumor with a diameter \> 5 cm;
  2. Multiple tumors with the largest tumor diameter \> 3 cm, with \< 5 tumors in total;
  3. Presence of portal vein tumor thrombus (Vp1-Vp2).
* Liver function: Child-Pugh score of 5-6.
* ECOG 0-1
* Life expectancy of at least 3 months.
* Women of childbearing potential (defined as not postmenopausal or surgically sterilized) must have a negative serum pregnancy test within 7 days prior to the study drug administration.
* Both women and men of childbearing potential must use reliable contraception during the study and for 60 days following the last dose of the study drug.
* For HBV-infected patients: If HBV-DNA is ≥ 10⁴ copies/ml within 14 days prior to enrollment, antiviral therapy (preferably entecavir) must be initiated to reduce HBV-DNA to \< 10⁴ copies/ml before entering the study. Antiviral therapy should continue, with regular monitoring of liver function and HBV-DNA levels.
* Adequate organ function.

Exclusion Criteria:

* Patients with distant metastasis.
* Patients with portal vein tumor thrombosis (Vp3-Vp4).
* History of any other malignant tumor within the past 5 years, unless the patient has received potentially curative treatment and there is no evidence of recurrence in the past 5 years. This 5-year time requirement does not apply to patients who have successfully undergone resection for basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, cervical carcinoma in situ, or other carcinoma in situ.
* History or current presence of congenital or acquired immunodeficiency diseases.
* Active or previously documented autoimmune diseases or inflammatory disorders (including but not limited to: autoimmune hepatitis, interstitial pneumonia, inflammatory bowel disease, systemic lupus erythematosus, vasculitis, uveitis, pituitary inflammation, hyperthyroidism or hypothyroidism, asthma requiring bronchodilators for treatment, etc.). Patients with vitiligo or asthma fully resolved in childhood and not requiring intervention as adults may be included.
* History of severe psychiatric disorders.
* Conditions affecting the absorption, distribution, metabolism, or elimination of the study drugs (e.g., severe vomiting, chronic diarrhea, bowel obstruction, malabsorption, etc.).
* Major surgery within 4 weeks prior to enrollment (as defined by the investigator).
* History of allogeneic stem cell or solid organ transplantation (except for corneal transplantation).
* Received other systemic antitumor therapies (including traditional Chinese medicine with antitumor indications) within 2 weeks or 5 half-lives (whichever is longer) prior to study drug administration, or unresolved adverse events related to prior treatments that have not recovered to ≤ CTCAE Grade 1.
* Use of systemic immunosuppressive drugs within 2 weeks prior to enrollment, or anticipated need for systemic immunosuppressive therapy during the study.
* Concurrent use of drugs that may prolong the QTc interval and/or induce Tdp, or drugs affecting drug metabolism.
* Known or suspected allergy to donafenib, recombinant humanized PD-1 monoclonal antibodies, or similar agents, or a history of hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins, or to excipients of the study drugs.
* Uncontrolled hepatic encephalopathy, hepatorenal syndrome, ascites, pleural effusion, or pericardial effusion.
* Active bleeding or coagulation disorders, bleeding tendencies, or ongoing treatment with thrombolytics, anticoagulants, or antiplatelet therapy.
* History of gastrointestinal bleeding or clear gastrointestinal bleeding tendencies within the past 6 months (e.g., known active ulcerative lesions, positive stool occult blood with ≥2+ results, requiring endoscopy if stool occult blood remains positive), or other conditions that may lead to gastrointestinal bleeding as determined by the investigator (e.g., severe esophageal/gastric varices).
* History of gastrointestinal perforation, abdominal fistulas, or intra-abdominal abscesses within the past 6 months.
* History of thrombosis or thromboembolic events (e.g., stroke, transient ischemic attack, deep vein thrombosis, pulmonary embolism) within the past 6 months.
* Significant cardiovascular disease, including but not limited to: acute myocardial infarction, severe/uncontrolled angina, coronary artery bypass grafting within the past 6 months; congestive heart failure (NYHA class \>2); poorly controlled arrhythmias requiring pacemaker treatment; drug-resistant hypertension (systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg).
* Active infection.
* Other significant clinical or laboratory abnormalities that may affect safety evaluation, such as uncontrolled diabetes, chronic kidney disease, grade 2 or higher peripheral neuropathy (CTCAE v5.0), thyroid dysfunction, etc.
* Use of live attenuated vaccines within 4 weeks prior to enrollment or during the study.
* Pregnant or breastfeeding women, or women or men of childbearing potential unwilling or unable to use effective contraception.
* History of alcohol, drug, or substance abuse within the past 6 months.
* Participation in any other clinical trial involving investigational drugs or medical devices within 4 weeks prior to enrollment.
* Inability to comply with the study protocol for treatment or follow-up visits.
* Any other conditions that, in the opinion of the investigator, would preclude participation in the study.

Where this trial is running

Fuzhou, Fujian and 2 other locations

• Fujian Cancer Hospital — Fuzhou, Fujian, China (Not_yet_recruiting)
• Fudan University Shanghai Cancer Center — Shanghai, Shanghai Municipality, China (Recruiting)
• TianJin Medical University Cancer Institute & Hospital — Tianjin, Tianjin Municipality, China (Not_yet_recruiting)

Study contacts

• Study coordinator: Lu Wang, M.D.

Conditions Hepato Cellular Carcinoma