Evaluation of the Safety and Efficacy of Sintilimab Combined With IBI305 in the Treatment of Advanced Hepatocellular Carcinoma in a Single-center, One-arm, and Phase Ib Study
Overview
- Phase
- Phase 1
- Intervention
- Sintilimab+IBI305
- Conditions
- Advanced Hepatocellular Carcinoma
- Sponsor
- Chinese Academy of Medical Sciences
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Incicende of Adverse Events (AEs)
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
This is a Phase Ib study to evaluate the safety, tolerability and efficacy of Sintilimab combined with IBI305 in patients with advanced hepatocellular carcinoma in China.
Detailed Description
This study is to evaluate the safety, tolerability and efficacy of Sintilimab combined with IBI305 in patients with advanced hepatocellular carcinoma in China. Approximately 26-38 subjects with locally advanced or metastatic hepatocellular carcinoma will be enrolled in the study. It includes dose escalation and dose expansion stage. 12-18 subjects will be enrolled in dose escalation stage for the safety and efficacy evaluation. Then select specific dose of IBI305 +Sintilimab 200mg/kg, expand to 20 patients for the further safety and efficacy study. The study treatment lasts up to 24 months, or until disease progresses, intolerable toxicity, withdrawal of informed consent, loss of follow-up, death, or other circumstances that require termination of treatment, whichever occurs first.
Investigators
Aiping Zhou
Chief physician
Chinese Academy of Medical Sciences
Eligibility Criteria
Inclusion Criteria
- •Local advanced or metastatic hepatocellular carcinoma, confirmed by histology/cytology.
- •Barcelona Clinic Liver Cancer (BCLC) C. BCLC B, unsuitable for local treatments or local treatments failure.
- •Patients who failed to or unsuitable for the previously systemic chemotherapy, sorafenib, lenvatinib, regorafenib or similar drug failure (disease progression or toxicity intolerance).
- •At least one measurable lesion per RECIST V1.1 that has not been treated locally or that has progressed after local treatment.
- •Child-Pugh score ≤ 7 points.
- •Adequate organ and bone marrow function.
Exclusion Criteria
- •With fibrous lamellar hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma, cholangiocarcinoma components in tumor tissues.
- •Have a history of hepatic encephalopathy or have a history of liver transplantation.
- •HBV DNA\>2000 IU/ml or 104 copies/ml for acute or chronic active hepatitis B or hepatitis C; HCV RNA\>103 copies/ml; both HbsAg and anti-HCV antibody are positive.
- •Esophageal or gastric varices bleeding caused by portal hypertension occurred in the past 6 months. Patients with endoscopy evidence of severe varices (G3) within 3 months. Patients with portal hypertension in high risk of bleeding evaluated by investigator.
- •History of venous thromboembolism in the past 6 months, including myocardial infarction, unstable angina, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis or any other history of severe thromboembolism. Implantable IV ports or catheter-derived thrombosis, superficial venous thrombosis, or thrombosis after conventional anticoagulant therapy are excluded. Prophylactic uses of low-dose aspirin or low molecular weight heparin is allowed.
- •Portal vein tumor thrombus (PVTT) involves both the main trunk and contralateral branch or upper mesenteric vein. Inferior vena cava tumor thrombus.
- •Uncontrolled high blood pressure, systolic blood pressure ≥150mmHg or diastolic blood pressure ≥100mmHg after optimal medical treatment; Hypertensive crisis or history of hypertensive encephalopathy.
- •History of gastrointestinal perforation and/or fistula in the past 6 months, history of intestinal obstruction (including incomplete intestinal obstruction requiring parenteral nutrition), extensive bowel resection (partial colectomy or extensive small bowel resection) , complicated by chronic diarrhea), Crohn's disease, ulcerative colitis or long-term chronic diarrhea.
- •History of interstitial pneumonia, drug-induced pneumonia, idiopathic pneumonia or active pneumonia. Allow radioactive pneumonia in the radiotherapy area.
- •Active tuberculosis (TB), who are receiving anti-tuberculosis treatment or who have received anti-tuberculosis treatment within 1 year before inclusion.
Arms & Interventions
Sintilimab+IBI305
Sintilimab: 200mg (D1, q3w） IBI305: 7.5mg/kg or 15mg/kg (D1, q3w）
Intervention: Sintilimab+IBI305
Outcomes
Primary Outcomes
Incicende of Adverse Events (AEs)
Time Frame: 2 years
Number of patients with AE, treatment-related AE (TRAE), immune-related AEs (irAE), AE of special interest (AESI), serious adverse event (SAE) assessed by CTCAE v5.0.
Secondary Outcomes
- Objective Response Rate (ORR)(2 years)
- Time to response (TTR)(2 years)
- Duration of response (DOR)(2 years)
- Disease control rate (DCR)(2 years)
- Progression free survival (PFS)(2 years)
- Overall Survival (OS)(2 years)
- Anti-drug antibody (ADA)(2 years)