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A Randomized Controlled Trial of Standard Of Care Versus Radio Ablation in Early Stage Hepatocellular Carcinoma

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This Phase II Prospective, parallel and open-label randomised control trial will investigate whether a radiotherapy technique (called SABR) can treat early stage liver cancer more effectively than current treatments which use heating probes directly inserted into the tumour or chemotherapy or radioactive particles injected into the blood supply of the tumour. Investigators hypothesize SABR will result in higher rates of freedom from local progression (FFLP) at 2 years compared to percutaneous thermal ablation ± TACE or transarterial therapies (TACE/TARE).The study will also look at other important outcomes such as progression free survival, overall survival, side effects, quality of life and people's experiences of their treatment.

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

⁃ 1\) Histological or radiological diagnosis of single, new HCC with largest diameter =8 cm (BCLC stage 0 or A).

• a) If prior history of HCC, the prior HCC must have been:

• Early stage, solitary HCC, =5 cm in size and,

• Have arisen within a different liver segment to the current HCC and,

• Treated with curative intent therapy \>2 years prior with no evidence of active disease at the site.

• 2\) As per local multidisciplinary HCC meeting consensus patient is suitable for percutaneous thermal ablation and/or transarterial therapies and not suitable for or declined liver resection and not planned for liver transplantation.

• 3\) Child-Pugh score =B7\* with no or diuretic-controlled ascites

• 4\) ECOG performance status =2

• 5\) Platelets =50x109/L, Haemoglobin =80 g/L, Neutrophils =1.0x109/L, INR \<1.8 (except if on therapeutic anticoagulation)

• 6\) 18 years of age or older and able to provide written consent

Locations
Other Locations
Australia
Trans Tasman Radiation Oncology Group
RECRUITING
Waratah
Canada
University Health Network - Princess Margaret Cancer Centre
RECRUITING
Toronto
Contact Information
Primary
Michael Yan, MD MPH FRCPC DABR
Michael.Yan@uhn.ca
(416) 946-2320
Time Frame
Start Date: 2026-05-11
Estimated Completion Date: 2032-04-01
Participants
Target number of participants: 218
Treatments
Experimental: Radiation Therapy
Other: Standard Of Care Treatment
Related Therapeutic Areas
Sponsors
Collaborators: Australasian Gastro-Intestinal Trials Group, Trans Tasman Radiation Oncology Group
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov