Holmium-166 Transarterial Radioembolization in Unresectable, Early Stage Hepatocellular Carcinoma.

Hepatocellular Carcinoma Clinical Trial

— HOMIE-166  

Official title:

Holmium-166 Transarterial Radioembolization in Unresectable, Early Stage Hepatocellular Carcinoma; a Prospective, Single-arm, Open Label, Multicenter Phase II Study: HOMIE-166.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05451862
• Other study ID #: T142E3
• Status: Recruiting
• Phase: N/A
• Start date: August 21, 2023
• Est. completion date: January 2031

Study information

• Verified date: September 2023
• Source: Terumo Europe N.V.
• Contact: Florence Chow
• Phone: +32(0)16 38 12 11
• Email: florence.chow[@]terumo-europe.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

166Ho-TARE is a promising modality for the treatment of HCC, given the unique characteristics of holmium, allowing careful patient selection and personalized dosimetry treatment planning. Further clinical evidence is needed to evaluate the safety and efficacy of 166Ho-TARE in the treatment of HCC patients with limited tumor burden, well preserved liver function and performance status and ineligible for liver transplantation and/or liver resection. This study will also provide further evidence on the dose-response relationship of 166Ho-TARE in (early) HCC.

Description:

This is a prospective, single-arm, open-label, multicenter study with 166Ho-TARE in unresectable HCC patients with limited tumor burden and well-preserved liver function and performance status, ineligible for liver transplantation and/or liver resection. Eligibility for liver transplantation and liver resection is determined by the multidisciplinary tumor board. However, patients eligible for liver transplantation can still be included in the setting of bridge to transplant.

The study proposes to use 166Ho-TARE, including both therapeutic 166Ho-microspheres (QuiremSpheres™ Holmium-166 Microspheres) and scout 166Ho-microspheres (QuiremScout™ Holmium-166 Microspheres). All patients providing informed consent and meeting the selection criteria will be further screened using a scout dose of 166Ho-microspheres to evaluate 166Ho-TARE eligibility. Patients not eligible for selective 166Ho-TARE are considered screen failures and will not be considered as enrolled.

The primary endpoint will be assessed by blinded, independent central review, organized by an imaging core laboratory.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 73
• Est. completion date: January 2031
• Est. primary completion date: January 2031
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age = 18 years

2. Multidisciplinary tumor board decision for locoregional treatment

3. Freely given, written informed consent

4. Patients with unresectable HCC with a single nodule = 8 cm or up to three nodules with a diameter of = 5 cm (each) eligible for selective radioembolization (including position changes of infusion catheters)

5. Non-cirrhotic patients or Child-Pugh A cirrhosis

6. ECOG performance status 0-1

7. Using an acceptable method of contraception throughout the study until survival follow up (for subjects of childbearing potential)

8. Adequate hematological, renal and liver function.

Adequate hematological function defined as:

• Hemoglobin = 6 mmol/L (9.7 g/dL)

• WBC = 3.0 x 10E9/L

• Absolute neutrophil count = 1.5 x 10E9/L

• Platelet count = 50,000/mm3

Adequate renal function defined as:

• Serum urea and serum creatinine < 1.5 times upper limit of normal (ULN)

• Creatinine clearance = 45 ml/min

Adequate liver function defined as:

• Total bilirubin = 35µmol/L (2.05 mg/dL)

• Albumin = 30 g/L

• AST and ALT = 5X ULN

Exclusion Criteria:

1. Diffuse and/or infiltrative HCC (defined as HCC consisting of multiple tiny liver nodules spreading throughout the entire liver or entire lobe, without a dominant nodule)

2. Hypoperfused HCC (defined as a lack of tumor blush (i.e. reduced or no uptake of contrast fluid) observed on the intra-procedural CT)

3. No full, selective arterial coverage on intra-procedural CT

4. Life expectancy < 6 months

5. Child-Pugh score =7 points

6. Prior liver transplantation

7. Prior locoregional or systemic anti-cancer therapy for HCC and previous malignancies

8. Macrovascular invasion (defined as macrovascular invasion of the hepatic and/or portal vein main branches)

9. Extrahepatic metastases

10. Clinically significant ascites

11. Hepatic encephalopathy

12. Untreated active hepatitis B and/or C

13. Work-up imaging showing:

• Lung shunt > 30 Gy is simulated on 166Ho-scout imaging; or

• Uncorrectable extrahepatic deposition of simulated 166Ho-scout dose activity. Activity in the falciform ligament, portal lymph nodes and gallbladder is accepted; or

• Anticipated ineffective tumor targeting (< 150 Gy mean tumor simulated absorbed dose) of 166Ho-scout for each lesion; or

• Entire tumor burden not within the perfused liver volume (possible extrahepatic collateral supply of the tumor); or

• Perfused liver volume > 50% of whole liver tissue

14. Pregnant or breast-feeding

15. Current or history of cancer other than HCC, except adequately treated non-melanoma skin cancer or carcinoma in situ of the cervix

16. In the Investigator's opinion there is a reason that could limit the patient's ability to participate in the study, compliance with follow-up requirements or impact the scientific integrity of the study

17. Concurrently enrolled in another study, unless it is an observational non-interventional study

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Hepatocellular
• Hepatocellular Carcinoma

Intervention

Device:
• Holmium-166 treatment
Implantation into hepatic tumors by delivery via the hepatic artery for the treatment of unresectable HCC liver tumors.
• Holmium-166 work-up
Evaluation of lung-shunt, extrahepatic deposition and intrahepatic distribution of intra-arterially injected microspheres for patients that are eligible for TARE treatment.

Locations

Country	Name	City	State
Germany	LMU Klinikum	Munich

Sponsors (1)

Lead Sponsor	Collaborator
Terumo Europe N.V.

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	confirmed Objective Response Rate (ORR) by localized mRECIST	ORR is defined as the proportion of patients achieving either complete or partial tumor response during the study, as assessed by blinded central image review according to localized mRECIST	5 years
Secondary	Best ORR based on localized mRECIST	The number and percent of patients with a confirmed response	5 years
Secondary	Best and confirmed ORR based on mRECIST	The number and percent of patients with a confirmed response	5 years
Secondary	Duration of Response (DoR) = 6 months based on localized mRECIST and mRECIST	The number and percent of patients with a DoR = 6 months. DoR is measured from time of initial response until radiological progression. Radiological progression is determined by blinded central image review according to localized mRECIST and mRECIST.	5 years
Secondary	Time to Progression (TTP)	TTP defined as the time from treatment with QuiremSpheresTM Holmium-166 Microspheres to progression as per mRECIST	5 years
Secondary	Progression-Free Survival (PFS)	PFS defined as the time from treatment with QuiremSpheresTM Holmium-166 Microspheres to the date of radiological progression or death from any cause. Radiological progression is determined by blinded central image review according to mRECIST	5 years
Secondary	hepatic Progression-Free Survival (hPFS)	hPFS defined as the time from treatment with QuiremSpheresTM Holmium-166 Microspheres to the date of radiological progression in the liver or death from any cause. Radiological progression is determined by blinded central image review according to mRECIST	5 years
Secondary	Liver transplantation rate	The number and percent of patients receiving a liver transplant	5 years
Secondary	Liver resection rate	The number and percent of patients undergoing a liver resection	5 years
Secondary	Overall survival (OS)	The median overall survival time	5 years
Secondary	Safety and toxicity by evaluating the number of adverse events and the number of patients with each event	Adverse events classified by Common Terminology Criteria for Adverse Events (CTCAE) v5.0. (including clinical and laboratory toxicity)	5 years
Secondary	Liver function during follow-up ALBI score	ALBI score	5 years
Secondary	Liver function during follow-up using MELD score	MELD score	5 years
Secondary	Liver function during follow-up using Child Pugh score	Child Pugh score	5 years
Secondary	Assessment of dosimetry and biodistribution based on quantitative assessment of imaging scans	Correlation between scout and treatment for extrahepatic dose deposition, including lung shunt and digestive shunting of QuiremSpheresTM Holmium-166 Microspheres.	5 years
Secondary	Assessment of dosimetry and biodistribution based on quantitative assessment of imaging scans	Correlation between treatment-based absorbed dose (into the tumor and healthy liver) and clinical outcomes in terms of toxicity and efficacy (i.e. radiological response).	5 years
Secondary	Assessment of dosimetry and biodistribution based on quantitative assessment of imaging scans	Correlation between scout-based simulated absorbed dose (into the tumor and healthy liver) and the treatment based absorbed dose (into the tumor and healthy liver).	5 years
Secondary	Quality of Life using EQ-5D-5L questionnaire	Patient reported outcome using EQ-5D-5L questionnaire. The scale measures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.	1 year