Tislelizumab Combined With IMRT Neoadjuvant Treatment for Resectable Hepatocellular Carcinoma With PVTT

NCT ID: NCT04850157

Last Updated: 2021-04-20

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-04-20
• Study Completion Date: 2023-12-20

Brief Summary

Due to the biological characteristics and liver anatomical characteristics of liver cancer, liver cancer cells easily invade the vascular system, especially the portal venous system, forming portal vein tumor thrombus (PVTT) , and its incidence is reported to be 44.0% ~ 62.2%. Once PVTT occurs in patients with liver cancer, the disease develops rapidly, and intrahepatic and extrahepatic metastasis, portal hypertension, jaundice, and abdominal effusion can occur in a short time with an average survival time of 2.7 months. PVTT is one of the major adverse factors for the prognosis of liver cancer and occupies an important weight influence in the clinical staging system of liver cancer. In some hepatocellular carcinoma (HCC) patients with PVTT and selective resectability, surgery versus non-surgery can lead to better survival of patients.

A retrospective analysis showed that neoadjuvant radiotherapy can reduce the extent of invasion of PVTT and improve postoperative survival in some HCC patients. Another prospective study showed that neoadjuvant radiotherapy could significantly improve the overall survival of resectable liver cancer with PVTT, and neoadjuvant radiotherapy could improve the 2-year survival of patients from 9.4% to 27.4% 27.4%, with an effective response of 20.7%.

This study is a prospective, single-center, single-arm study to assess the efficacy and safety of neoadjuvant therapy with tislelizumab combined with IMRT for resectable liver cancer with PVTT.

Conditions

Hepatocellular Carcinoma With Portal Vein Tumor Thrombus

Study Design

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

Study Groups

Tislelizumab+IMRT

Group Type: EXPERIMENTAL

Tislelizumab

Intervention Type: DRUG

200mg, Q3W

IMRT

Intervention Type: RADIATION

4 Gy\* 5 Fx,5Fx/Week

Interventions

Tislelizumab

200mg, Q3W

Intervention Type: DRUG

IMRT

4 Gy\* 5 Fx,5Fx/Week

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed hepatocellular carcinoma
• Patients with at least one measurable lesion
• Resectable primary lesion, PVTTⅡ-Ⅲtype
• No previous treatment for hepatocellular carcinoma
• Eastern Cooperative Oncology Group(ECOG): Performance Status(PS)score 0-1
• Child-Pugh score A
• Expected survival ≥ 3 months
• Baseline blood routine and blood biochemical indicators should meet the following criteria:

hemoglobin ≥ 90 g/L, absolute neutrophil count ≥ 1.5 × 10 ^/L, platelet count ≥ 75 × 10 ^/L aspartate or alanine aminotransferase 5 times the upper limit of normal (ULN), alkaline phosphatase ≤ 2.5 times the ULN, serum albumin ≥ 30 g/L; serum creatinine 1.5 times the ULN; international normalized ratio (INR)) ≤ 2 or prothrombin time (PT) more than the upper limit of normal range ≤ 6 seconds

• Appropriate to participate in this trial as assessed by the investigator before entering the study
• Male and female subjects of childbearing potential must agree to use an effective method of contraception throughout the study
• Signed informed consent.

Exclusion Criteria

• Imaging showed distant metastasis
• Previous treatment with other effective regimens (including surgery, radiotherapy, systemic therapy, etc.)
• Previous allergic reactions to the same kind of drugs
• Pregnant or lactating patients
• Active hepatitis B or C (hepatitis B: HBsAg positive and Hepatitis B (HBV )DNA ≥ 1*10^4 IU/ml; hepatitis C: hepatitis C virus (HCV) antibody and HCV RNA positive, requiring simultaneous antiviral therapy)
• Pericardial effusion, uncontrolled pleural effusion or clinically severe ascites at screening
• History of interstitial lung disease, pneumonitis, or uncontrolled systemic disease, including diabetes, hypertension, pulmonary fibrosis, acute lung disease
• Suffering from severe cardiovascular disease within 12 months before screening, such as symptomatic coronary heart disease,≥II congestive heart failure, uncontrolled arrhythmia, infarction, etc
• Any active immunodeficiency or autoimmune disease at screening and/or any history of immunodeficiency or autoimmune disease that may recur (such as hypothyroidism or hyperthyroidism, interstitial pneumonia, enteritis, hepatitis, hypophysitis, vasculitis, myocarditis, etc.)
• Use of steroids or other systemic immunosuppressive therapy 14 days before enrollment; use of steroids or other systemic immunosuppressive therapy
• Patients with other previous malignancies that are not cured; Patients with other previous malignancies that are not cured
• Immunocompromised patients, such as immunocompromised patients, such as human immunodeficiency virus (HIV) positive; positive
• With uncontrollable psychosis; With uncontrollable psychosis
• Other factors make the investigators think it is inappropriate to participate in this trial.

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

Sponsors

Shanghai Zhongshan Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Zhongshan hospital, Fudan University

Shanghai, , China

Countries

China

Central Contacts

Xinrong Yang

Role: CONTACT

yang.xinrong@zs-hospital.sh.cn

86-13764295279

Facility Contacts

Xinrong Yang

Role: primary

yang.xinrong@zs-hospital.sh.cn

Other Identifiers

B2020-187R-1

Identifier Type: -

Identifier Source: org_study_id