Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06349317

Neoadjuvant IMRT Combined With Camrelizumab and Apatinib for Resectable HCC With PVTT

Neoadjuvant Intensity-modulated Radiotherapy Combined With Perioperative Camrelizumab and Apatinib in the Treatment of Resectable Hepatocellular Carcinoma Associated With Portal Vein Tumor Thrombus: a Single-arm Prospective Clinical Study

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
33 (estimated)
Sponsor
Yongyi Zeng · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is an open-label, single-arm prospective clinical trial that evaluates the efficacy and safety of neoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinib in the treatment of resectable hepatocellular carcinoma with portal vein tumor thrombus.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTNeoadjuvant intensity-modulated radiotherapy combined with perioperative camrelizumab and apatinib1. Preoperative IMRT targeting PVTT and intrahepatic tumor lesions with a prescribed dose for 18Gy in 6 fractions delivered by using 6-MV X-rays with a linear accelerator at 5 fractions per week; 2. Perioperative combination of camrelizumab and apatinib Preoperatively, camrelizumab (200mg, every 2 weeks) combined with apatinib (250mg, daily) for 2 cycles (2 weeks as one cycle); Postoperatively, camrelizumab (200mg, every 3 weeks) combined with apatinib (250mg, daily) for 8 cycles (3 weeks as one cycle).

Timeline

Start date
2024-04-22
Primary completion
2026-05-01
Completion
2026-06-01
First posted
2024-04-05
Last updated
2025-09-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06349317. Inclusion in this directory is not an endorsement.