Clinical trial · Interventional
Sunitinib and Chemoembolization in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery
A Phase II Study of SUNITINIB MALATE (Sutent) and Chemoembolization in Patients With Unresectable Hepatocellular Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): low accrual
Summary
Brief summary (as posted)
RATIONALE: Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Chemoembolization kills tumor cells by blocking the blood flow to the tumor and keeping chemotherapy drugs, such as doxorubicin, near the tumor. Giving sunitinib together with chemoembolization may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving sunitinib together with chemoembolization works in treating patients with liver cancer that cannot be removed by surgery.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Liver Cancer | Malignant Liver Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (5)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| doxorubicin hydrochloride | Drug | Doxorubicin | ALIAS |
| hepatic artery embolization | Procedure | — | UNRESOLVED |
| laboratory biomarker analysis | Other | — | UNRESOLVED |
| quality-of-life assessment | Procedure | — | UNRESOLVED |
| sunitinib malate | Drug | Sunitinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Sunitinib
- description
- oral sunitinib malate once daily on days 1-7 and 15-35 in course 1 and on days 1-28 in all subsequent courses
- interventionNames
- Drug: doxorubicin hydrochloride
- Drug: sunitinib malate
- Other: laboratory biomarker analysis
- Procedure: hepatic artery embolization
- Procedure: quality-of-life assessment
Primary outcomes (1)
- measure
- Progression-free Survival
- timeFrame
- From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
- description
- median progression free survival in months
Secondary outcomes (5)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 120 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically, cytologically, or serologically\* confirmed hepatocellular carcinoma meeting the following criteria: * 1-4 lesions * Involvement of 1 or both liver lobes NOTE: \*Alpha-fetoprotein (AFP) \> 500 mcg/L in high-risk patients * Measurable disease by CT scan or MRI * Disease does not exceed 50% of the liver parenchyma * At least 1 lesion ≥ 3 cm in longest diameter * Tumor burden involves \< 50% of the liver * Refused surgery OR unresectable disease due to any of the following: * Multifocality * Advanced cirrhosis * Comorbid illness * Candidate for chemoembolization * No fibrolamellar histology * No ascites * No known brain metastases PATIENT CHARACTERISTICS: * ECOG performance status 0-2 * Life expectancy ≥ 12 weeks * WBC ≥ 3,000/mm³ * ANC ≥ 1,500/mm³ * Hemoglobin ≥ 8.5 g/dL (transfusion allowed) * Platelet count ≥ 100,000/mm³ * Bilirubin ≤ 2 mg/dL * AST ≤ 5 times upper limit of normal (ULN) * INR \< 1.5 * Creatinine ≤ 2.0 mg/dL OR creatinine clearance ≥ 30 mL/min * No bleeding diathesis or coagulopathy * No active congestive heart failure * No uncontrolled angina * No myocardial infarction within the past 12 months * No cardiac arrhythmia * Ejection fraction ≥ 45% (in patients with known coronary artery disease and in patients \> 50 years of age) * Child-Pugh class A or B cirrhosis * No impedance of hepatopedal blood flow (portal vein thrombosis) * No thrombosis of the main portal vein * No encephalopathy * No biliary obstruction * No variceal bleed within the past 6 months * No history of allergic reactions attributed to compounds of similar chemical or biologic composition to sunitinib malate * No absolute contraindication to doxorubicin, iodinated contrast material, microfibrillar collage hemostat, or dexamethasone * No other concurrent uncontrolled illness including, but not limited to, any of the following: * Ongoing or active infection * Psychiatric illness or social situation that would limit compliance with study requirements * No other active malignancies within the past year except nonmelanoma skin cancer or carcinoma in situ * No significant traumatic injury within the past 4 weeks * No QTc prolongation (i.e., QTc interval ≥ 500 msec) or other significant ECG abnormalities * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception during and for 6 months after the completion of study treatment PRIOR CONCURRENT THERAPY: * Recovered from prior therapy * Prior liver-directed therapy, such as chemoembolization, radiofrequency ablation, cryoablation, or ethanol injection allowed if the following criteria are met: * Treated lesion remains inactive by CT scan or MRI and new lesion being embolized is distinct from the previously treated lesion * Radiographic progression of previously treated lesion requiring re-embolization * Prior liver resection allowed * Prior immunotherapy allowed * No prior antiangiogenesis therapy * No prior liver transplantation * Patients awaiting a cadaveric or orthotopic liver transplantation are eligible provided they have end-stage liver disease with a priority score of \< 20 points * More than 4 weeks since prior radiotherapy or chemotherapy (6 weeks for nitrosoureas or mitomycin C) * More than 4 weeks since prior major surgery or open biopsy * At least 1 week since prior fine needle biopsy * No concurrent immunotherapy * No concurrent radiotherapy * No concurrent combination antiretroviral therapy for HIV-positive patients * No concurrent therapeutic doses of coumarin-derivative anticoagulants (e.g., warfarin) * Doses of ≤ 1 mg/day are allowed for prophylaxis of thrombosis as long as INR ≤ 1.5 * Both full dose and prophylactic dose low molecular weight heparin allowed as long as PT INR ≤ 1.5 * No anticipated major surgery during and for 3 months after completion of study treatment * No other concurrent investigational agents * No other concurrent anticancer therapy
References
Publications (0)
Data not yet available