Comparison of Efficacy in SBRT of Large HCC With or Without TACE

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age30-80
SponsorBeijing 302 Hospital

About this trial

The study aims to compare efficacy and adverse reactions of large hepatocellular carcinoma participants (5-10cm) who receive stereotactic body radiation therapy with or without transcatheter arterial chemoembolization.The investigators will optimize the combined treatment schedule of SBRT for hepatocellular carcinoma participants by comparing overall survival rates, progression-free survival rates and local control and adverse reaction occurrence rates in the two groups.

Eligibility criteria

Qualifiers

primary HCC diagnosed by a surgeon and/or radiologist and oncologist according to the international guidelines for the management of HCC or by pathology

single lesion and longest tumor diameter were 5-10cm;

CP-A or B classification;

Eastern Cooperative Oncology Group (ECOG) score 0-1;

Disqualifiers

tumor thrombus;

lymph node involvement;

extrahepatic metastasis.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 2 trial groups

Sponsors and collaborators