Single Arm, Prospective, Multicenter Clinical Study of TACE With Adebrelimab and Bevacizumab for Unresectable Hepatocellular Carcinoma

NCT ID: NCT05970666

Last Updated: 2024-02-28

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 71 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-15
• Study Completion Date: 2026-11-15

Brief Summary

To evaluate the efficacy and safety of TACE combined with adebrelimab and bevacizumab transformation in unresectable hepatocellular carcinoma

Conditions

Adebrelimab; Hepatocellular Carcinoma; Transformation; Bevacizumab; TACE

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single arm

Group Type: EXPERIMENTAL

TACE with adebrelimab and bevacizumab

Intervention Type: DRUG

TACE treatment once; Adebrelimab: 20mg/kg, every 3 weeks (21 days); Bevacizumab; 15mg/kg, every 3 weeks (21 days);

Interventions

TACE with adebrelimab and bevacizumab

TACE treatment once; Adebrelimab: 20mg/kg, every 3 weeks (21 days); Bevacizumab; 15mg/kg, every 3 weeks (21 days);

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age: 18 ~ 75, both male and female；

2. Strictly comply with the primary liver cancer diagnosis and treatment standard (2022 edition) clinical diagnosis criteria or primary hepatocellular carcinoma diagnosed by pathological histology or cytology examination, and at least one measurable lesions (according to the RECIST1.1 standard, the spiral CT scan of 10mm or short diameter of 15mm）；

3. Patients without previous systematic treatment and inoperable resection / radical ablation surgery, but who can tolerate TACE;

4. The CNLC stage is Ⅱa-Ⅲb stage;

5. The Child-Pugh grade of liver function is A grade or B grade (5-7 points);

6. The ECOG PS score is 0-1 points;

7. Expected survival period of 12 weeks;

8. If the patient has active hepatitis B virus (HBV) infection: HBV-deoxyribonucleic acid (DNA) must be <2000 IU / mL (if the study site has only copy / mL testing units, Must be <12500 copy / mL), And received at least 14 days before initiating anti-HBV treatment (according to local standard therapy, e. g. entecavir) and willing to receive antiviral treatment throughout the study; hepatitis C virus (HCV) ribonucleic acid (RNA) positive patients must receive antiviral treatment according to local standard treatment guidelines and liver function within grade CTCAE 1 elevation;

9. Main organs function are normal and meet the following criteria: (1) The blood routine examination standards should be met with: (no blood transfusion within 14 days) A. Hemoglobin (HB), 90g / L, B. White blood cell count (WBC) 3109 / L C. Absolute neutrophil count (ANC) 1.5109 / L, D. Platelet (PLT) 80109 / L;(2) Biochemical examination shall meet the following standards: A. Bilirubin (BIL) <1.5 times the upper limit of normal value (ULN); B. Glutamic gamma aminotransferase (ALT) and glutamate aminotransferase AST <5 ULN; C. Serum creatinine (Cr)≤1.5ULN；

10. Women of childbearing age must have negative pregnancy test (serum) or urine HCG within 7 days before enrollment and are willing to use appropriate contraception during treatment and 24 weeks after the last administration of test drug; for men, surgical sterilization or agree to use appropriate contraception during and 24 weeks after the last administration of trial drug;

11. The subjects volunteered to join the study and had good compliance with the follow-up.

Exclusion Criteria

1. Pregnant or lactating women;

2. The pathology is clearly cholangiocytic carcinoma or mixed cell carcinoma;

3. Diffuse liver cancer;

4. Patients with autoimmune diseases, organ / hematopoietic stem cell transplantation or other malignant tumors (except for cured basal skin cell carcinoma and cervix carcinoma in situ);

5. Patients with consciousness disorders or unable to cooperate with the treatment, combined with patients with mental illness;

6. Patients who have participated in other clinical trials in the recent three months;

7. Previous history of other malignancies or have received targeted therapy and other PD-1 / PD-L1 inhibitor therapy;

8. Received major surgery or chemotherapy or other systemic therapy for target lesions (including not limited to radiation therapy, ablation therapy, etc.) within 1 month prior to enrollment;

9. Use of immunosuppressants or systemic hormone therapy within 14 days before enrollment to achieve immunosuppressive purposes (dose> 10mg / day prednisone or other efficacy hormones);

10. Liver function was graded as Child-Pugh C, which could not be improved by liver care treatment；

11. esophageal (gastric fundus) varices rupture and bleeding within 1 month before treatment；

12. Uncorrectable coagulopathy and severe blood abnormalities, with severe bleeding tendency. Platelet count <50109 / L and severe coagulation abnormalities against surgery (anticoagulation therapy and / or anticoagulant therapy should be stopped for more than 1 week before radiation therapy);

13. A stubborn amount of ascites, pleural fluid, malignant fluid;

14. Active infection, especially the inflammation of the biliary tract system;

15. Severe functional failure of the liver, kidney, heart, lung, brain and other major organs;

16. Previously allergic to PD-1 / PD-L1 mAb / any component of the targeted drug or other similar trials;

17. Patients with hypertension who cannot be reduced to the normal range by antihypertensive medication (systolic blood pressure> 140 mmHg, diastolic blood pressure> 90 mmHg);

18. Previous severe cardiovascular disease, including but not limited to the following diseases: myocardial ischemia or myocardial infarction, poorly controlled arrhythmia (including 450 ms in QTc men and 470 ms in women); cardiac dysfunction by NYHA, or cardiac ultrasound indicating left ventricular ejection fraction (LVEF) <50%;

19. Patients with positive urinary protein (urinary protein test of 2 + or above, or 24-hour urinary protein quantification of> 1.0g);

20. Failure to swallow tablets, malabsorption syndrome, or any condition affecting gastrointestinal absorption;

21. According to the discretion of the investigator, patients with other concomitant diseases that seriously endanger patient safety or affect the completion of the study;

22. Patients with radiotherapy, targeted therapy, and other contraindications to immunotherapy.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Jiangsu HengRui Medicine Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

The First Affiliated Hospital of Xiamen University

OTHER

Sponsor Role: lead

Responsible Party

Jianbo Chen

director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jianbo Chen

Role: PRINCIPAL_INVESTIGATOR

The First Affiliated Hospital of Xiamen University

Feng Ye

Role: PRINCIPAL_INVESTIGATOR

The First Affiliated Hospital of Xiamen University

congren Wang

Role: STUDY_DIRECTOR

Quanzhou First Hospital

Qinghe Cai

Role: STUDY_DIRECTOR

Affiliated Hospital of Putian University

Jiafei Chen

Role: STUDY_DIRECTOR

Putian First Hospital

Yongzhong Wang

Role: STUDY_DIRECTOR

Sanming Second Hospital

Feng Lin

Role: STUDY_DIRECTOR

Ningde Mindong Hospital

Locations

The First Affiliated Hospital of Xiamen University

Xiamen, Fujian, China

Site Status: RECRUITING

Countries

China

Central Contacts

Jianbo Chen

Role: CONTACT

274439002@qq.com

15605921022

Facility Contacts

Jianbo Chen

Role: primary

274439002@qq.com

15605921022

Other Identifiers

23-OBU-FJ-HCC-II-012

Identifier Type: -

Identifier Source: org_study_id