©2025 Stanford Medicine
HepaSphere/Quadrasphere Microspheres for Delivery of Doxorubicin for the Treatment of Hepatocellular Cancer
Not Recruiting
Trial ID: NCT01387932
Purpose
The purpose of this study is to evaluate overall survival in patients diagnosed with hepatocellular cancer (HCC) treated with HepaSphere/QuadraSphere Microspheres loaded with chemotherapeutic agent doxorubicin compared to conventional transarterial chemoembolization with particle PVA, lipiodol, and doxorubicin.
Official Title
Phase 3 Prospective, Randomized, Blinded, and Controlled Investigation of HepaSphere/QuadraSphere Microspheres for Delivery of Doxorubicin for the Treatment of Hepatocellular Carcinoma
Stanford Investigator(s)
Daniel Sze, MD, PhD
Professor of Radiology (Interventional Radiology)
Gloria Hwang, MD
Clinical Professor, Radiology
David S. Wang, MD
Clinical Associate Professor, Radiology
John D. Louie, MD
Clinical Professor, Radiology
WILLIAM T. KUO, MD, FSIR, FCCP, FSVM, FACR, FCIRSE
Professor of Radiology (Interventional Radiology)
Nishita Kothary, MD
Professor of Radiology (Interventional Radiology)
Lawrence "Rusty" Hofmann, MD
Professor of Radiology (Interventional Radiology)
David Hovsepian, MD
Clinical Professor, Radiology - Pediatric Radiology
Eligibility
Inclusion Criteria:
Patients must meet all of the following inclusion criteria in order to be entered into the study:
1. Age 18 or older
2. Patient has signed informed consent
3. Patient must have a diagnosis of hepatocellular cancer confirmed by at least one of the following:
i. Histological confirmation ii. Magnetic resonance imaging (MRI) result with early enhancement and delayed enhancement washout of at least one solid liver lesion \> 1 cm. Patient must also have evidence of cirrhosis or have chronic hepatitis B.
iii. Contrast enhanced computed tomography (CT) with early enhancement and delayed enhancement washout of at least one solid liver lesion \> 1cm. Patient must also have evidence of cirrhosis or have chronic hepatitis B.
d. Patient must not be suitable for treatment by resection or percutaneous ablation at time of study entry.
Patients not suitable for ablation due to lesion location may be enrolled
e. Patient MUST meet at least ONE of the following criteria:
i. Stage Child-Pugh B 7 ii. Recurrent HCC iii.Performance status ECOG 1
f. Patient has a life expectancy of at least 6 months
g. Absence of occlusive thrombus to the main portal trunk
Exclusion Criteria:
If patients meet any of the following criteria they may not be entered into the study:
1. Current or previous treatment with chemo- or radiation therapy or sorafenib
2. Previous treatment with any form of transarterial embolization for HCC
3. Patients with current or history of any other cancer except non-melanomatous skin cancer
4. Female patients who are pregnant, breastfeeding, or premenopausal and not using an effective method of contraceptive
5. Performance status ECOG \> 2
6. Child-Pugh scores \>7
7. Active gastrointestinal bleeding
8. Evidence of uncorrectable bleeding diathesis
9. Extra-hepatic spread of the HCC
10. Total Bilirubin \> 3 mg/dL
11. \>50% tumor involvement of the liver
12. Infiltrative or diffuse HCC
13. Encephalopathy not adequately controlled medically
14. Presence of ascites not controlled medically
15. Presence of medically relevant localized or systemic infection, other than hepatitis B, C, D, E or G
16. Any contraindication for MRI (eg. metallic implants)
17. Allergy to contrast media that cannot be managed with prophylaxis
18. Allergy to iodized oil
19. Any contraindication to arteriography
20. Any contraindication for doxorubicin administration, including the following:
i. White Blood Cell count (WBC) \<3000 cells/mm₃
ii. Absolute Neutrophil \<1500 cells/mm₃
iii. Cardiac ejection fraction \<50%
iv. Other condition deemed exclusionary by physician
u. Any contraindication for hepatic embolization, including the following:
i. Porto-systemic shunt, or an arteriovenous shunt that cannot be adequately closed prior to chemoembolization
ii. Hepatofugal blood flow
iii. Serum creatinine \> 2mg/dL
iv. Uncorrectable impaired clotting
1. Platelet \<50,000/mm₃
2. International Normalized Ratio (INR) \> 1.4
3. Activated Prothrombin Time (aPTT) less than 21 or greater than 40
v. AST \> 5X upper limit of normal for lab
vi. ALT \> 5X upper limit of normal for lab
Intervention(s):
device: HepaSphere/QuadraSphere Microspheres
procedure: PVA, lipiodol, doxorubicin
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
CCTO
650-498-7061