Individualized Dosimetry for Holmium-166 Radioembolization in Patients With Unresectable Hepatocellular Carcinoma

Trial Title: Individualized Dosimetry for Holmium-166 Radioembolization in Patients With Unresectable Hepatocellular Carcinoma

NCT ID: NCT06302400

Condition: Carcinoma, Hepatocellular

Conditions: Official terms:
Carcinoma
Carcinoma, Hepatocellular

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Device
Intervention name: 166Holmium microspheres (QuiremSpheres®)
Description: QuiremSpheres® are a biocompatible microsphere that contain the radionuclide holmium-166 (166Ho), which emits gamma-radiation (81 keV) and high-energy (1.81 MeV) beta-particles.
Arm group label: Radioembolisation with 166Holmium microspheres

Summary: The goal of this clinical trial is to test the safety and effectiveness of a medical device called 166-Holmium microspheres (QuiremSpheres®) in patients with hepatocellular carcinoma (HCC) . The main questions it aims to answer are: - What is the safety and toxicity profile of the 166-Holmium microspheres? - Is the device effective in treating HCC? Participants will undergo a range of screening procedures to confirm they are eligible and to record their baseline results, including: - A Computed Tomography (CT) scan - A Magnetic Resonance Imaging (MRI) scan - Blood tests - Quality of life questionnaires Before receiving treatment with QuiremSpheres® the participant will receive a 'scout' dose of the microspheres, to check whether there is distribution of the radioactivity to other non-target areas of the body. This is measured using Single-Photon Emission Computed Tomography-CT imaging. If the distribution to non-target areas is deemed to not be too high, the participant will go on to receive the individualised therapeutic dose of QuiremSpheres®. Follow-up visits will occur 3 and 6 weeks post-treatment dose, and then at 3 and 6 months.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Provided written informed consent. 2. Female or male aged 18 years and over. 3. Diagnosis of HCC established according to AASLD criteria: nodule >1 cm in a patient at risk for HCC, with combination of arterial hypervascularity and venous or delayed phase wash-out on multiphase CT-scan or MRI-scan. LR-5 and LR- 4 based on Liver Imaging Reporting and Data System can be included. 4. No curative treatment options (resection, transplant, or in case of solitary tumour, RFA). 5. Life expectancy of at least 6 months. 6. ECOG Performance status 0-1. 7. Liver-dominant disease (maximum 5 lung nodules all ≤1.0 cm, solitary clinically stable adrenal metastasis, and mesenteric or portal lymph nodes all ≤2.0 cm are accepted). 8. Child-Pugh class A5-6 or B7. 9. At least one measurable liver lesion according to the modified RECIST criteria. 10. Negative pregnancy test for women of childbearing potential. Female patients of childbearing potential should use a highly effective acceptable method of contraception (oral contraceptives, barrier methods, approved contraceptive implant, long-term injectable contraception, intrauterine device or tubal ligation) or should be more than 1 year postmenopausal or surgically sterile during their participation in this study (from the time they sign the consent form), to prevent pregnancy. Exclusion Criteria: 1. Evidence of significant extrahepatic disease (MRI-scan liver and multiphase abdominal CT as well as a thoracic CT are routinely performed at screening). 2. Hepatic radiation therapy within the last 4 weeks before the start of study therapy. 3. Previous or current treatment with RE. Previous treatment with TACE, surgery, RFA, and previous or current treatment with systemic treatment are allowed. 4. Major surgery within 4 weeks or incompletely healed surgical incision before starting study therapy. 5. Serum bilirubin > 34 umol/L in the absence of a reversible cause 6. Glomerular filtration rate <35 ml/min. 7. Non-correctable INR >1.5 in case of femoral approach (as opposed to radial). 8. Platelet count <50 109/l. 9. Significant cardiac event (e.g., myocardial infarction, superior vena cava (SVC) syndrome, New York Heart Association (NYHA) classification of heart disease ≥2) within 3 months before entry, or presence of cardiac disease that in the opinion of the investigator increases the risk of ventricular arrhythmia. 10. Pregnancy or breastfeeding. 11. Patients suffering from psychic disorders that make a comprehensive judgment impossible, such as psychosis, hallucinations and/or depression. 12. Patients who are declared incapacitated. 13. Previous enrolment in the present study. 14. Male patients who are not surgically sterile or do not use an acceptable method of contraception during their participation in this study (from the time they sign the consent form), to prevent pregnancy in a partner. 15. Evidence of untreated, clinically significant grade 3 portal hypertension (i.e. large varices at oesophagi-gastro-duodenoscopy). In these cases, therapy with non-selective beta-blocker (propranolol) or rubber band ligation should be instituted according to accepted guidelines. In case of small varices, prophylactic propranolol is advised. 16. Portal vein thrombosis (tumour and/or bland) of the main branch (diagnosed on contrast enhanced transaxial images). Involvement of the right or left portal vein branches and more distal is accepted. 17. Untreated active hepatitis. In case of detectable viral HBV load, appropriate treatment should be instituted. 18. Transjugular intrahepatic portosystemic shunt (TIPS). 19. Body weight over 150 kg (because of maximum table load). 20. Severe allergy for intravenous contrast used (Visipaque®) 21. Lung shunt >30 Gy, as calculated using scout dose SPECT/CT. 22. Extrahepatic deposition of scout dose activity. Activity in the falciform ligament, portal lymph nodes and gallbladder is accepted.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Imperial College Healthcare NHS Trust

Address:
City: London
Zip: W12 0HS
Country: United Kingdom

Status: Recruiting

Contact:
Last name: Rohini Sharma, Professor

Phone: 02033133720
Email: r.sharma@imperial.ac.uk

Start date: February 22, 2024

Completion date: February 2027

Lead sponsor:
Agency: Imperial College London
Agency class: Other

Collaborator:
Agency: Terumo Europe N.V.
Agency class: Industry

Source: Imperial College London

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06302400