Combining Donafenib and Envafolimab for Patients at High Risk of Liver Cancer Recurrence

Adjuvant Treatment of Patients With High Risk of Recurrent Hepatocellular Carcinoma After Radical Surgery With Donafenib in Combination With Envafolimab: a Prospective, Multicentre, Single-arm Phase II Clinical Study

This study is testing if a new combination of two drugs, donafenib and envafolimab, can help prevent liver cancer from coming back in patients who have just had surgery for it and are at high risk for recurrence.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 45 (estimated)
• Ages: 18 Years to 80 Years
• Sex: All
• Sponsor: Anhui Provincial Hospital (Government)
• Drugs / interventions: Envafolimab, radiation, prednisone, immunotherapy
• Locations: 2 sites (Fuyang, Anhui and 1 other locations)
• Trial ID: NCT06498622 on ClinicalTrials.gov

What this trial studies

This multi-center, single-arm study evaluates the safety and efficacy of donafenib in combination with envafolimab for patients who have undergone surgery for hepatocellular carcinoma (HCC) and are at high risk for recurrence. The study aims to address the lack of standard postoperative adjuvant therapies by exploring this combination treatment in patients with specific high-risk factors. Participants will be closely monitored for recurrence and overall survival outcomes following their surgical treatment.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18-80 with primary hepatocellular carcinoma who have undergone curative surgery and have specific high-risk factors for recurrence.

Not a fit: Patients with recurrent or metastatic disease, significant comorbidities, or those who have received prior antitumor therapies may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could significantly reduce the risk of recurrence and improve survival rates for patients with hepatocellular carcinoma.

How similar studies have performed: While various adjuvant treatments for hepatocellular carcinoma are being explored, this specific combination of donafenib and envafolimab is novel and has not been extensively tested in prior studies.

Eligibility criteria

Inclusion Criteria:

* 18-80 years old, male and female.
* Subjects voluntarily enrolled in this study and signed the informed consent, good compliance and co-operated with the follow-up.
* Primary hepatocellular carcinoma with postoperative histopathological diagnosis of HCC and negative margins.
* Presence of any of the following high-risk factors for recurrence: ① tumor size ≥5.0cm combined with microvascular invasion; ② number of tumors ≥3; ③ presence of portal vein cancer thrombus (vp1 or vp2 type).
* No recurrence of metastasis confirmed by imaging examination 3-7 weeks after surgery.
* ECOG score of 0-1.
* Expected survival ≥ 3 months.
* Child-Pugh score ≤ 7.
* Subjects with no previous antitumour therapy (except antiviral therapy)
* No extra-hepatic metastases or lymph node metastases.
* No significant abnormality in routine laboratory tests (blood test, liver and kidney function, coagulation function, etc.): (1) Criteria for routine blood tests need to be met (no blood and blood products transfusion within 14 days): a. Absolute neutrophil value (ANC) ≥ 1.5\*10\^9/L; b. Haemoglobin (HGB) ≥ 90g/L; c. Platelet count (PLT) ≥ 75\*10\^9/L. (2) Biochemical tests need to meet the following criteria: a. Serum albumin (ALB) ≥ 35g/L; b. Serum total bilirubin (TBIL) \< 1.5\*Upper Limit of Normal (ULN); c. Serum glutamic transaminase (AST), alanine aminotransferase (ALT) \< 2.5\*ULN; d. Serum creatinine ≤ 1.5\*ULN.

Exclusion Criteria:

* Previous histologically/cytologically confirmed fibroplaque-containing hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma, cholangiocarcinoma and other components.
* Histologically confirmed positive resection margin (R1 resection), presence of lymph node metastasis or extrahepatic metastasis.
* Previous or current malignancy other than hepatocellular carcinoma.
* History of hepatic encephalopathy or history of liver transplantation.
* Previous history of allergy to any component of the test drug: Envafolimab monoclonal antibody, donafini.
* Subjects with poorly controlled persistent postoperative pleural, abdominal or pericardial effusion.
* Previous antitumour therapy (except antiviral therapy).
* History of interstitial lung disease (except radiation pneumonitis not treated with hormones), non-infectious pneumonia.
* Presence of any active autoimmune disease or history of autoimmune disease in the subject (e.g., the following, but not limited to: autoimmune hepatitis, interstitial pneumonitis, uveitis, enterocolitis, hepatitis, pituitary gland inflammation, vasculitis, nephritis, hyperthyroidism, hypothyroidism subjects with vitiligo or asthma that has been in complete remission in childhood and does not require any intervention in adulthood may be enrolled subjects with asthma that requires medical intervention with bronchodilators cannot be included).
* Subjects who are on immunosuppressive, or systemic, or absorbable topical hormone therapy for immunosuppression (dose \>10mg/day prednisone or other equipotent hormone) and continue to use it within 2 weeks prior to enrolment.
* A serious infection (CTCAE \> grade 2) such as severe pneumonia, bacteraemia, or infectious co-morbidities requiring hospitalisation has occurred 4 weeks prior to the first use of study drug.
* Subjects who have experienced acute cardiovascular disease such as acute cerebral infarction, acute coronary syndrome, etc. within 1 month, with cardiovascular clinical symptoms or disease not well controlled.
* According to NYHA standard, grade III to IV cardiac insufficiency, or cardiac ultrasound examination suggests that the left ventricular ejection fraction (LVEF) \<50%
* Uncontrollable hypertension with treated systolic blood pressure \> 140 mmHg or diastolic blood pressure \> 90 mmHg, hypertensive crisis or history of hypertensive encephalopathy
* Patients with a definite tendency to gastrointestinal bleeding, including the following: patients with locally active ulcerative lesions and fecal occult blood {(++) may not be enrolled} those with a history of black stools and vomiting of blood within 2 months.
* Those with abnormal coagulation function (INR\>1.5 APTT\>1.5 ULN) and bleeding tendency.
* Prolonged unhealed wounds or fractures major surgical procedures or severe traumatic injuries, fractures or ulcers within 4 weeks.
* Subjects with congenital or acquired immune deficiency (e.g., HIV-infected individuals), or active hepatitis (Hepatitis B reference: HBV DNA test value exceeds the upper limit of normal Hepatitis C reference: HCV viral titre or RNA test value exceeds the upper limit of normal).
* Patients with a history of psychotropic substance abuse that cannot be stopped or patients with mental disorders.
* Patients with concomitant illnesses that, in the investigator's judgement, are a serious hazard to patient safety or interfere with the patient's ability to complete the study.
* Pregnant women, lactating women, and women of childbearing age who are not using adequate contraception.
* In the judgement of the investigator, Patients who are not suitable for inclusion.

Where this trial is running

Fuyang, Anhui and 1 other locations

• No.2 People's Hospital of Fuyang city — Fuyang, Anhui, China (Recruiting)
• Anhui province hospital — Hefei, Anhui, China (Recruiting)

Study contacts

• Principal investigator: Lianxin Liu — Anhui Provincial Hospital
• Study coordinator: Lianxin Liu

Conditions Hepatocellular Carcinoma