Phase 2 Study of Stereotactic Body Radiation Therapy Plus Tislelizumab and Regorafenib in Unresectable or Oligometastatic Hepatocellular Carcinoma

Status: Recruiting
Location: See location...
Intervention Type: Combination product
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this phase 2 prospective clinical trial is to learn about the efficacy and safety of stereotactic body radiation therapy (SBRT) plus immunotherapy and targeted therapy in patients with unresectable or oligometastatic hepatocellular carcinoma (HCC). The main question to answer is: Whether combing SBRT with immunotherapy and targeted therapy could prolong PFS. Participants will receive SBRT to all visible lesions and concurrent systemic immunotherapy and targeted therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• age ≥ 18 years

• Eastern Cooperative Oncology Group performance status of 0-1

• clinical or pathological diagnosis of HCC

• with unresectable locally advanced or oligometastatic HCC (metastatic lesions ≤ 5, metastatic organs ≤ 3, may involve extrahepatic lymph nodes or distant organs apart from brain)

• at least one measurable lesion according to mRECIST criteria

• all lesions could be included in radiation target volume

• Child-Pugh A or B (7 scores) liver function

• patients are allowed to receive systemic therapy previously other than tislelizumab plus regorafenib

• adequate hematological and renal function

• life expectancy ≥ 3 months;

• willing to participate in the study and give written informed consent

Locations
Other Locations
China
Peking University Cancer Hospital
RECRUITING
Beijing
Time Frame
Start Date: 2023-06
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 39
Treatments
Experimental: SBRT plus Tislelizumab and Regorafenib
Participants will receive SBRT (8 Gy × 3-5 fractions) to all visible lesions. Systemic treatment (tislelizumab and regorafenib) will start concurrently and last for 2 years, or until disease progression, intolerable side-effects or death. Tislelizumab will be delivered every 21 days at a dose of 200mg, and regorafenib will be given at a dose of 120mg for the first 21 days of a 28-day cycle. Appropriate dose adjustments of regorafenib will be made if side-effects are intolerable, while the dose of tislelizumab should not be adjusted, but could be paused.
Related Therapeutic Areas
Sponsors
Leads: Peking University Cancer Hospital & Institute

This content was sourced from clinicaltrials.gov