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- Klinische proef NCT07584018
The DoHAICs Study Expansion Phase
7 mei 2026 bijgewerkt door: Tianjin Medical University Cancer Institute and Hospital
Clinical Study on the Efficacy and Safety of Donafenib Combined With Hepatic Artery Infusion Chemotherapy and Sintilimab as the First-line Treatment for Unresectable Hepatocellular Carcinoma - the DoHAICs Study Expansion Phase
We explored the efficacy and safety of the first-line treatment of unresectable hepatocellular carcinoma with donafenib combined with hepatic artery infusion chemotherapy (HAIC) and sintilimab .
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
90
Fase
- Fase 2
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Voluntarily participate in the trial and provide written informed consent.
- Age between 18 and 80 years (inclusive), regardless of gender.
- Patients with hepatocellular carcinoma (HCC) clinically diagnosed per the "Standard for Diagnosis and Treatment of Primary Liver Cancer (2024 Edition)" or confirmed by histology/cytology.
- Patients with inoperable or metastatic hepatocellular carcinoma.
- No prior systemic therapy for advanced disease. Patients who received adjuvant chemotherapy following local therapy are eligible if chemotherapy was completed >12 months ago and disease progression or metastasis has occurred.
- Completion of the last interventional therapy, radiotherapy, or ablation therapy >4 weeks prior.
- For patients with prior hepatectomy, resection must have been R0, and tumor recurrence must have occurred more than 24 months after surgery.
- At least one measurable lesion as defined by RECIST 1.1 criteria.
- Life expectancy ≥3 months.
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.
- Child-Pugh score ≤7.
- Able and willing to comply with the protocol for the observation of adverse events and efficacy.
- Adequate organ function, defined as meeting the following criteria:
- Hematological function (without transfusion or granulocyte colony-stimulating factor [G-CSF] support within 14 days prior to screening):
- Hemoglobin ≥90 g/L.
- Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L.
- Platelet count ≥75 × 10⁹/L.
- Biochemical tests (without albumin infusion within 14 days prior to screening):
- Albumin ≥28 g/L.
- Total bilirubin ≤2 × upper limit of normal (ULN).
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤5 × ULN.
- Alkaline phosphatase (ALP) ≤5 × ULN.
- Serum creatinine ≤1.5 × ULN.
- Coagulation function:
- International normalized ratio (INR) or prothrombin time (PT) ≤1.5 × ULN.
- Activated partial thromboplastin time (APTT) ≤1.5 × ULN.
Exclusion Criteria:
- Histologically/cytologically confirmed components such as fibrolamellar hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma, or cholangiocarcinoma.
- History of malignancies other than hepatocellular carcinoma, except under the following circumstances:
- The patient has undergone potentially curative treatment with no evidence of that disease for 5 years.
- Successfully resected basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the cervix, or other carcinoma in situ.
- Diffuse tumor lesions.
- History of hepatic encephalopathy, hepatorenal syndrome, or liver transplantation.
- Clinically symptomatic pleural effusion, ascites, or pericardial effusion requiring drainage.
- Central nervous system metastases.
- History of severe psychiatric illness.
- Diseases affecting the absorption, distribution, metabolism, or excretion of the investigational drug (e.g., severe vomiting, chronic diarrhea, intestinal obstruction, malabsorption, etc.).
- Prior allogeneic stem cell or solid organ transplantation.
- Prior treatment with anti-VEGF/VEGFR, RAF, MEK pathway targeted therapies (e.g., sorafenib, lenvatinib, regorafenib) or immunomodulators (e.g., anti-PD-1, anti-PD-L1, anti-CTLA-4 antibodies).
- Prior other systemic anti-tumor therapy, including Chinese herbal medicine with anti-tumor indications, completed less than 2 weeks before study drug initiation; or patients with adverse events from prior therapy not recovered to ≤ Grade 1 per CTCAE (excluding alopecia and Grade 1/2 neuropathy caused by oxaliplatin).
- Concurrent use of medications known to prolong QTc interval and/or induce Torsades de Pointes (TdP), or medications that affect drug metabolism.
- Past or present congenital or acquired immunodeficiency diseases.
- Active or history of autoimmune or inflammatory diseases (including but not limited to: autoimmune hepatitis, interstitial pneumonia, inflammatory bowel disease, systemic lupus erythematosus, vasculitis, uveitis, hypophysitis, hyper- or hypothyroidism, asthma requiring bronchodilators, etc.). Patients with vitiligo or asthma that was fully resolved in childhood and requires no intervention in adulthood may be included.
- Use of systemic immunosuppressive medication within 2 weeks prior to enrollment, or anticipated requirement for such medication during the study, except for:
- Intranasal, inhaled, topical, or local corticosteroid injections (e.g., intra-articular).
- Systemic corticosteroids at physiological doses not exceeding 10 mg/day prednisone or equivalent.
- Prophylactic use of corticosteroids for hypersensitivity reactions.
- Known or suspected hypersensitivity to donafenib, drugs of the same class, or history of hypersensitivity to chimeric or humanized antibodies or fusion proteins, or allergy to any excipient of the investigational drug.
- Active bleeding or coagulation disorders, bleeding tendency, or undergoing thrombolytic, anticoagulant, or antiplatelet therapy.
- Thrombotic or thromboembolic events within the past 6 months, such as stroke and/or transient ischemic attack, deep vein thrombosis, pulmonary embolism, etc.
- History of esophageal or gastric variceal bleeding due to portal hypertension within the past 6 months, or any life-threatening bleeding event within the past 3 months.
- Significant cardiovascular disease, including but not limited to: acute myocardial infarction, severe/unstable angina, or coronary artery bypass grafting within the past 6 months; congestive heart failure (NYHA class >2); poorly controlled arrhythmias requiring pacemaker treatment; uncontrolled hypertension (systolic BP ≥140 mmHg and/or diastolic BP ≥90 mmHg).
- Other clinically significant abnormalities, deemed by the investigator to affect safety evaluation, such as uncontrolled diabetes, chronic kidney disease, Grade II or higher peripheral neuropathy (CTCAE v6.0), abnormal thyroid function, etc.
- Active or poorly controlled severe infection; active infections including:
- Positive for Human Immunodeficiency Virus (HIV) (HIV1/2 antibodies).
- Active Hepatitis B (HBsAg positive or HBV DNA >2000 IU/mL with abnormal liver function).
- Active Hepatitis C (HCV antibody positive or HCV RNA ≥10³ copies/mL with abnormal liver function).
- Active tuberculosis.
- Other uncontrolled active infections (CTCAE v6.0 > Grade 2).
- Incomplete recovery from surgery, such as unhealed wounds or severe postoperative complications.
- Pregnancy, lactation, or patients of childbearing potential unwilling or unable to use effective contraception.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Donafenib combined with hepatic artery infusion chemotherapy and sintilimab
Donafenib combined with hepatic artery infusion chemotherapy and sintilimab injection as the first-line treatment for unresectable hepatocellular carcinoma
|
Donafenib (200 mg twice daily, taken orally, initiated 3-7 days before the first HAIC session)
sintilimab (200 mg intravenously every 3 weeks, administered 0-1 day before each HAIC treatment)
HAIC (oxaliplatin 85 mg/m2 over 2 hours, leucovorin 400 mg/m2 over 2 hours, bolus fluorouracil 400 mg/m2 within the first 10 minutes, followed by fluorouracil infusion 1200 mg/m2 over 23 hours, every 3 weeks.)
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
event-free survival
Tijdsspanne: The time from enrollment to the date of first documented progression, recurrence, or death from any cause, whichever came first, assessed up to 36 months
|
The time from enrollment to the date of first documented progression, recurrence, or death from any cause, whichever came first, assessed up to 36 months
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
20 mei 2026
Primaire voltooiing (Geschat)
1 juni 2027
Studie voltooiing (Geschat)
1 juni 2027
Studieregistratiedata
Eerst ingediend
22 december 2025
Eerst ingediend dat voldeed aan de QC-criteria
7 mei 2026
Eerst geplaatst (Werkelijk)
13 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
13 mei 2026
Laatste update ingediend die voldeed aan QC-criteria
7 mei 2026
Laatst geverifieerd
1 december 2025
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- E20251318
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .