Combination of SFRT, PD-L1 Inhibitor, and Anti-VEGF in Advanced Hepatocellular Carcinoma

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorGuiping People's Hospital

About this trial

PD-1 inhibitor plus anti-VEGFR has become the established standard first-line systemic treatment for unresectable hepatocellular carcinoma (HCC). Despite an improved objective response rate (ORR) of around 30%, the majority of patients face HCC progression and liver failure. Developing a new combined treatment strategy to overcome resistance to anti-PD-L1 and anti-VEGF is essential to improve patient outcomes. Stereotactic radiotherapy (SBRT) can enhance immune response through various mechanisms, and its immunomodulatory effect has been confirmed in multiple solid tumors. However, due to the limitation of the OAR tolerance dose, large-volume tumors are unsuitable for SBRT treatment. To overcome this issue, researchers have introduced the spatially fractionated radiation therapy (SFRT) mode, which allows for a highly uneven radiation dose distribution within the tumor volume. SFRT is an emerging radiotherapy technique with high clinical response rates and low radiation-related toxicity in large-volume solid tumors. Therefore, the investigators conducted this single-arm, single-arm, open-label study to evaluate the efficacy and safety of SFRT combined with PD-1 inhibitors and anti-VEGFR in unresectable HCC. The primary endpoint is objective response rate (ORR), and secondary endpoints include overall survival (OS), progression-free survival (PFS), and toxicity.

Eligibility criteria

Qualifiers

Age: 18-75 years old;

Eastern Cooperative Oncology Group (ECOG) -Performance Status(PS):0-1 points;

Patient clinically or pathologically diagnosed with hepatocellular carcinoma;

Advanced hepatocellular carcinoma that is inoperable

Disqualifiers

Prior invasive malignancy unless disease-free for a minimum of 2 years

Prior radiotherapy to the region of the liver that would result in overlap of radiation therapy fields

Prior selective internal radiotherapy/ablation, at any time

Untreated active hepatitis B or hepatitis C

Trial design

Treatments tested in this trial

  • Combination of SFRT, PD-L1 inhibitor, and Anti-VEGF

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators

Guiping People's Hospital

Lead sponsor

Youjiang Medical College for Nationalities

Sponsor institution