Impact of Radiotherapy on ctDNA in Patients With Hepatocellular Carcinoma

NCT ID: NCT06885879

Last Updated: 2025-04-10

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 15 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-04-08
• Study Completion Date: 2028-07-31

Brief Summary

Radiotherapy is increasingly being used in the management of hepatocellular carcinoma (HCC) as a standalone treatment, or in combination with systemic therapy. Stereotactic Body Radiation Therapy (SBRT) causes cell death directly (via double-stranded breaks) and indirectly (via vascular bed damage or promotion of antitumour immunity). Unfortunately, the effect of cell death is not immediate and takes time. As a result, the typical arterial phase hyperenhancement on imaging may persist up to 12 months after radiotherapy, and it is not necessarily suggestive of presence of viable tumours. Therefore, there is no consensus on ideal timing of response assessment following radiotherapy to HCC. Therefore, a blood-based biomarker which can be done frequently and monitored dynamically, could be preferred for response assessment after radiotherapy. Circulating tumour DNA (ctDNA) is an emerging and promising biomarker in cancer management, which has been shown useful in cancer screening, guiding treatment, and informing prognosis. Currently, most of the clinical applications of ctDNA revolve around either the presence of ctDNA, or the genomic changes associated with these molecules. Biological properties of ctDNA such as fragment length, jaggedness of fragments, or epigenetic changes may provide additional information related to the tumour characteristics and its sensitivity to anti-cancer treatments. These biological properties of ctDNA are relatively unexplored in the context of radiotherapy. It is unknown whether these properties can be utilized for monitoring treatment response. We therefore propose to study the biological properties of ctDNA in relation to HCC patients undergoing radiotherapy.

Conditions

HCC - Hepatocellular Carcinoma

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Study Groups

Temporal change of fragmentomics of Circulating tumour DNA investigation

Temporal change of fragmentomics of Circulating tumour DNA undergoing Stereotactic Body Radiation Therapy investigation

Intervention Type: RADIATION

Patients will have blood taking for Circulating tumour DNA (ctDNA) (20cc each) at Week 0 (before radiotherapy), Week 1 (during radiotherapy), Week 2 (after radiotherapy), Week 12 and Week 24.

Radiological assessment will be performed before radiotherapy, Week 12 (approximately 3 months post treatment) and Week 24-26 (approximately 6 months post treatment).

Interventions

Temporal change of fragmentomics of Circulating tumour DNA undergoing Stereotactic Body Radiation Therapy investigation

Patients will have blood taking for Circulating tumour DNA (ctDNA) (20cc each) at Week 0 (before radiotherapy), Week 1 (during radiotherapy), Week 2 (after radiotherapy), Week 12 and Week 24.

Radiological assessment will be performed before radiotherapy, Week 12 (approximately 3 months post treatment) and Week 24-26 (approximately 6 months post treatment).

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

• Patients aged ≥ 18 years old
• Eastern Cooperative Oncology Group (ECOG) performance 0 to 1
• Confirmed diagnosis of Hepatocellular carcinoma (HCC)
• Tumour size ≥ 3cm
• Patients planning on undergoing Stereotactic Body Radiation Therapy (SBRT) for HCC
• Prior radiofrequency ablation at a different site, or prior surgery are eligible
• Child-Pugh A liver function
• Life expectancy longer than 12 weeks
• At least one measurable treatment lesion according to RECIST 1.1
• Written informed consent must be obtained prior to any study related procedures
• Adequate haematological function (Hemoglobin ≥ 8.5g/dL; Platelet Count ≥ 75x109/L; Antenatal Care ≥ 1.5x109/L; international normalised ratio ≤ 1.5)
• Adequate hepatic function (albumin ≥ 28g/l; Bilirubin ≤ 1.5xULN; Alanine transaminase < 5 times upper limit normal)
• Adequate renal function (serum creatinine ≤ 1.5 times the upper limit of normal range; Sodium ≥ 130mmol/L; Potassium ≥ 3.0mmol/L)
• Able to read, understand and provide written consent

Exclusion Criteria

• Histology shows sarcomatoid HCC, fibrolamellar HCC, mixed cholangiocarcinoma-hepatocellular carcinoma
• Presence of other malignancy than HCC within 5 years from diagnosis of HCC
• Prior Transarterial chemoembolization (TACE) within 3 months
• Previous radiotherapy to the abdomen
• Previous yttrium-90 chemoembolization
• Repetitive history of non-healing wounds or ulcers within 2 months of inclusion
• Pregnant or lactating females at any time during the study
• Active autoimmune disease requiring systemic therapy in the past 2 years
• Diagnosis of immunodeficiency (including Human Immunodeficiency Viruses)
• Patients with coagulopathy or on anticoagulant will be excluded from liver biopsy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Chinese University of Hong Kong

OTHER

Sponsor Role: lead

Responsible Party

Landon Chan

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Department of Clinical Oncology, Prince of Wales Hospital

Hong Kong, , Hong Kong

Site Status: RECRUITING

Countries

Hong Kong

Central Contacts

Landon L CHAN, MSc, MBChB

Role: CONTACT

landon.chan@cuhk.edu.hk

+852 3505 1042

Natalie KWONG

Role: CONTACT

nataliekwong019@cuhk.edu.hk

+852 3505 1040

Facility Contacts

Landon L CHAN

Role: primary

landon.chan@cuhk.edu.hk

MSc, MBChB

Natalie, KWONG

Role: backup

nataliekwong019@cuhk.edu.hk

+852 3505 1040

Other Identifiers

TRA025

Identifier Type: -

Identifier Source: org_study_id