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- Essai clinique NCT07594340
HAIC vs. TACE Combined With Sintilimab and Bevacizumab for Intermediate HCC (Beyond Up-To-Seven)
Hepatic Arterial Infusion Chemotherapy Plus Sintilimab and Bevacizumab Versus Transarterial Chemoembolization Plus Sintilimab and Bevacizumab for Intermediate-Stage Hepatocellular Carcinoma Beyond the Up-To-Seven Criteria:A Prospective, Randomized, Controlled Trial
The purpose of this prospective, randomized, multicenter, controlled clinical study is to evaluate the efficacy and safety of hepatic arterial infusion chemotherapy (HAIC) compared to transarterial chemoembolization (TACE) when both are combined with sintilimab and bevacizumab for patients with intermediate-stage hepatocellular carcinoma (HCC). Specifically, the trial focuses on patients with a high tumor burden that exceeds the Up-To-Seven criteria.While TACE is the standard treatment for BCLC stage B HCC, its effectiveness is often limited in patients with extensive intrahepatic tumor loads. This study investigates whether the combination of FOLFOX-HAIC and systemic therapy (sintilimab plus bevacizumab) provides better local control and survival outcomes than the combination of TACE and the same systemic therapy.
Experimental Group: Patients receive FOLFOX-HAIC (up to 4 cycles in the first 16 weeks) combined with sintilimab and bevacizumab. Control Group: Patients receive on-demand TACE (up to 4 cycles in the first 16 weeks) combined with sintilimab and bevacizumab. Primary Objective: To compare Progression-Free Survival (PFS) between the two arms as evaluated by mRECIST. Enrollment: A total of 300 patients will be randomized at a 1:1 ratio to the treatment groups. The study aims to provide high-level clinical evidence for optimizing treatment strategies for this specific subgroup of HCC patients.
Aperçu de l'étude
Statut
Les conditions
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Wei He
- Numéro de téléphone: +8618666014207
- E-mail: hewei@sysucc.org.cn
Lieux d'étude
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Guangdong
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Guangzhou, Guangdong, Chine, 510000
- Recrutement
- Sun Yat-sen University Cancer Center
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Contact:
- Wei He
- Numéro de téléphone: 15521248313
- E-mail: hewei@sysucc.org.cn
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Chercheur principal:
- Binkui Li
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Diagnosis: Histologically or cytologically confirmed hepatocellular carcinoma (HCC), or patients with cirrhosis meeting the American Association for the Study of Liver Diseases (AASLD) clinical diagnostic criteria for HCC.
- Age: ≥ 18 years old.
- Performance Status: ECOG performance status score of 0.
- Prior Treatment: No prior systemic anti-tumor therapy or transarterial interventional therapy for HCC.
- Tumor Stage and Burden: Barcelona Clinic Liver Cancer (BCLC) Stage B, unsuitable for radical surgery and/or local therapy (such as ablation).
- Up-To-Seven Criteria: Tumor burden exceeding the Up-To-Seven criteria, defined as the sum of the size of the largest intrahepatic tumor (in cm) and the number of tumors being greater than 7.
- Tumor Distribution: Bilobar multifocal tumors.
- Measurable Disease: At least one measurable lesion with arterial phase enhancement on CT/MRI.
- Vascular Status: Patent portal vein with no evidence of portal vein tumor thrombus.
- Extrahepatic Status: No extrahepatic metastasis.
- Variceal Risk: No risk of variceal bleeding; esophagogastroduodenoscopy (EGD) within 6 months shows no gastroesophageal varices or active ulcers.
- Liver Function: Child-Pugh Grade A.
- Hematology: Platelets > 75 × 10⁹/L; White Blood Cells > 3.0 × 10⁹/L; Neutrophils > 1.5 × 10⁹/L.
- Biochemistry: Serum bilirubin ≤ 1.5 × upper limit of normal (ULN); Transaminases ≤ 3 × ULN; Serum creatinine < 1.5 × ULN.
- Physical Findings: No ascites
- Albumin ≥ 30 g/L.
- Coagulation: Normal coagulation function.
- Expectancy: Expected survival > 3 months.
- Consent: Signed written informed consent and willingness/ability to comply with follow-up until death, study completion, or termination.
Exclusion Criteria:
- Histology: Known histology/cytology of fibrolamellar HCC, sarcomatoid HCC, or components of cholangiocarcinoma.
- Medical History: History of hepatic encephalopathy or liver transplantation.
- Effusions: Clinically symptomatic pleural effusion, ascites, or pericardial effusion requiring drainage.
- Viral Hepatitis: Active Hepatitis B (HBV DNA > 2000 IU/ml or 10⁴ copies/ml) or Hepatitis C (HCV RNA > 10³ copies/ml); co-infection with both HBsAg and anti-HCV positive. (Eligible if levels drop below these criteria after nucleoside antiviral therapy) .
- Cardiovascular (Past 12 Months): Myocardial infarction, severe/unstable angina, coronary artery bypass grafting, congestive heart failure, cerebrovascular accident (including transient ischemic attack), or pulmonary embolism.
- Ongoing Cardiac Issues: Arrhythmia ≥ Grade 2 (NCI-CTCAE); QTc prolongation (Male > 450 ms, Female > 470 ms).
- Bleeding Risk: History of gastrointestinal bleeding within 6 months or clear bleeding tendency (e.g., high-risk varices, active GI ulcer, persistent positive fecal occult blood).
- Hypertension: Uncontrollable hypertension (SBP > 140 mmHg or DBP > 90 mmHg despite optimal treatment); history of hypertensive crisis or hypertensive encephalopathy.
- Organ Failure: Renal failure requiring hemodialysis or peritoneal dialysis; severe dysfunction of other major organs.
- Second Malignancy: History of other malignancies within 3 years prior to screening (except those with negligible risk of metastasis/death such as treated cervical cancer in situ, non-melanoma skin cancer, or localized prostate cancer).
- CNS Involvement: Known or new evidence of brain or leptomeningeal lesions. Coagulation Disorders: Hemophilia or bleeding tendency; currently taking therapeutic doses of coumarin derivatives (e.g., warfarin).
- Pregnancy/Lactation: Pregnant or breastfeeding females; women of childbearing potential must have a negative pregnancy test within 7 days prior to enrollment.
- Other History: Prior organ transplant; known HIV infection; active tuberculosis; allergy to chemotherapy drugs.
- Autoimmune Diseases: Active or history of autoimmune diseases (e.g., myasthenia gravis, myositis, autoimmune hepatitis, SLE, rheumatoid arthritis, IBD, etc.).
- General Compliance: Any serious acute/chronic physical or mental illness, or laboratory abnormalities that increase study risk or interfere with interpretation of results.
- Non-compliance: History of significant non-compliance with medical protocols or inability to provide reliable informed consent.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: FOLFOX-HAIC Combination
Intervention: Drug (Sintilimab): 200mg IV Q3W (Up to 12 months). Drug (Bevacizumab): 15mg/kg IV Q3W (Up to 12 months). Procedure (FOLFOX-HAIC): Max 4 cycles within first 16 weeks. Oxaliplatin: 130mg/m² infusion (2h). Leucovorin: 400mg/m² infusion (2h). 5-FU: 400mg/m² bolus (10min) + 1200mg/m² infusion (23h). |
Drug (Sintilimab): 200mg IV Q3W (Up to 12 months).
Drug (Bevacizumab): 15mg/kg IV Q3W (Up to 12 months).
Procedure (FOLFOX-HAIC): Max 4 cycles within first 16 weeks.
Oxaliplatin: 130mg/m² infusion (2h).
Leucovorin: 400mg/m² infusion (2h).
5-FU: 400mg/m² bolus (10min) + 1200mg/m² infusion (23h).
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Comparateur actif: TACE Combination
Intervention: Drug (Sintilimab): 200mg IV Q3W (Up to 12 months). Drug (Bevacizumab): 15mg/kg IV Q3W (Up to 12 months). Procedure (TACE): On-demand (max 4 cycles within 16 weeks). Epirubicin (30mg/m²) + Lobaplatin (30-50mg) + Lipiodol (5-20ml). |
Drug (Sintilimab): 200mg IV Q3W (Up to 12 months).
Drug (Bevacizumab): 15mg/kg IV Q3W (Up to 12 months).
Procedure (TACE): On-demand (max 4 cycles within 16 weeks).
Epirubicin (30mg/m²) + Lobaplatin (30-50mg) + Lipiodol (5-20ml).
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Progression-Free Survival
Délai: From date of randomization until the date of first documented progression (per mRECIST) or date of death from any cause, assessed up to 5 years.
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Progression-Free Survival (PFS): From randomization to first documentation of progression (mRECIST) or death from any cause.
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From date of randomization until the date of first documented progression (per mRECIST) or date of death from any cause, assessed up to 5 years.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Overall Survival
Délai: From date of randomization until the date of death from any cause, assessed up to 5 years.
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Overall Survival (OS): From randomization to death from any cause.
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From date of randomization until the date of death from any cause, assessed up to 5 years.
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Objective Response Rate
Délai: From date of randomization until the end of systemic treatment (up to 12 months).
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Objective Response Rate (ORR): Proportion of patients with CR or PR per mRECIST and RECIST 1.1.
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From date of randomization until the end of systemic treatment (up to 12 months).
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Disease Control Rate
Délai: From date of randomization until the end of systemic treatment (up to 12 months).
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Disease Control Rate (DCR): Proportion of patients with CR, PR, or SD.
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From date of randomization until the end of systemic treatment (up to 12 months).
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Duration of Response
Délai: From initial response (CR or PR) to the date of first documented progression or death,assessed up to 5 years.
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From initial response (CR or PR) to the date of first documented progression or death
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From initial response (CR or PR) to the date of first documented progression or death,assessed up to 5 years.
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Time to Progression
Délai: From date of randomization to the date of first objective tumor progression, assessed up to 5 years.
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From date of randomization to the date of first objective tumor progression
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From date of randomization to the date of first objective tumor progression, assessed up to 5 years.
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Conversion Rate
Délai: From date of randomization until the end of the conversion therapy assessment (typically within 12 months).
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Conversion Rate: Percentage of patients achieving surgical resection eligibility.
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From date of randomization until the end of the conversion therapy assessment (typically within 12 months).
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Safety Profile
Délai: From randomization until 1 year after the last dose of study treatment.
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Safety Profile: Incidence of adverse events per NCI CTCAE v5.0.
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From randomization until 1 year after the last dose of study treatment.
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Patient-Reported Outcomes
Délai: Baseline and every 1 month until the end of month 12.
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Patient-Reported Outcomes (PRO): Quality of life using IL42-EORTC QLQ-C30.
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Baseline and every 1 month until the end of month 12.
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Binkui Li, Sun Yat-sen University Cancer Center
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Tumeurs par type histologique
- Tumeurs du système digestif
- Maladies du système digestif
- Maladies du foie
- Tumeurs, glandulaires et épithéliales
- Adénocarcinome
- Tumeurs du foie
- Carcinome
- Carcinome hépatocellulaire
- Thérapeutique
- Thérapie biologique
- Immunomodulation
- Immunothérapie
Autres numéros d'identification d'étude
- B2026-143-01
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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