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NCT Number: NCT07628751

A Study of Standard Of Care Versus Radio Ablation in Early Stage HCC

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Trans Tasman Radiation Oncology Group, Waratah, Australia

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About this study

The SOCRATES randomised controlled trial will assess the efficacy, toxicity, HRQoL profile and cost effectiveness of SABR compared to the current SOC treatment in patients with first diagnosis of unresectable, single nodule HCC. Participants will be placed into one of two groups based on the size of their tumour and whether thermal ablation is an appropriate treatment for them. The study will include about 218 participants in total. Participants will be randomly assigned to receive either SABR or the current standard of care. Standard care may include thermal ablation, transarterial chemoembolisation (TACE), or transarterial radioembolisation (TARE).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 1) Presence of multifocal HCC, macrovascular invasion or extrahepatic disease
  • 2) Prior treatment for any HCC within last 2 years.
  • 3) Clinically evident ascites or hepatic encephalopathy
  • 4) Prior abdominal radiation therapy that would preclude the delivery of protocol defined SABR to the tumour.
  • 5) Untreated Hepatitis B or C
  • 6) Known additional invasive malignancy (excluding non-melanoma skin cancer) that is progressing or required treatment within the last 2 years.
  • 7) Pregnancy

Treatment and study plan

Stereotactic Ablative Body Radiotherapy (SABR)

Radiation

SABR will be delivered in 3 or 5 outpatient treatment sessions (each 20 to 45 minutes in duration) spaced out over 1 to 2 weeks. The exact number of treatment sessions received, and the duration of each session depends on the size and location of the liver cancer.

Therapies

Radiation

Patients will receive standard of care treatment (SOC) as per their institution's local practice that will be administered by a doctor called an Interventional Radiologist. The therapies offered will depend on the size and location of the liver cancer and may include one or a combination of radiofrequency ablation (RFA) / microwave ablation (MWA) and/or transarterial chemoembolization (TACE) / transarterial radioembolisation (TARE).

Primary outcomes

  1. Freedom from local progression (FFLP)

    Time frame: 2 years

Secondary outcomes

  1. Progression-free survival (PFS)

    Time frame: 2 years

  2. Overall survival (OS)

    Time frame: 2 years

  3. Safety and adverse events (CTCAE v5.0)

    Time frame: 2 Years

  4. Patient reported outcomes (EORTC QLQ-C30)

    Time frame: 2 Years

    The C30 is a 30-item instrument that evaluates HRQOL comprised of five functional scales (physical, cognitive, emotional, social, and role) as well as nine symptom scales (fatigue, pain, nausea/vomiting, dyspnea, insomnia, anorexia, constipation, diarrhea, and financial), and a global QoL scale.

    Responses are scored on a linear scale from 0 to 100. Higher scores on functioning/global health indicate a better, healthier state. Higher scores on symptom scales indicate a higher symptom burden or worse condition.

  5. Patient reported outcomes (QLQ-HCC18)

    Time frame: 2 Years

    QLQ-HCC18 is a questionnaire where patients report symptoms or problems on a scale of 1 (not much) to 4 (very much). Higher scores on symptom scales indicate a higher symptom burden or worse condition.

  6. Cost-effectiveness analysis

    Time frame: 2 Years

    Incremental cost per outcome

Study contacts

Contact information is provided by the study sponsor or research team.

Michael Yan, MD MPH FRCPC DABR

CONTACT

[email protected]

(416) 946-2320

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Australasian Gastro-Intestinal Trials Group
  • Trans Tasman Radiation Oncology Group

Registry information

Official study title

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

Acronym: SOCRATES HCC

Important dates

Study start
2026
Primary completion
2032
Study completion
2032
First posted
Jun 5, 2026
Registry last updated
Jun 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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