Decentrialz logo
  • HIPAA Compliant
  • ISO 27001 Certified
Find Trials
About UsContact
Become a Volunteer+1 877 705 1914

Status:

COMPLETED

Floxuridine and Dexamethasone as a Hepatic Arterial Infusion and Bevacizumab in Treating Patients With Primary Liver Cancer That Cannot be Removed by Surgery

Lead Sponsor:

Memorial Sloan Kettering Cancer Center

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Liver Cancer

Eligibility:

All Genders

18-120 years

Phase:

PHASE2

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as floxuridine and dexamethasone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. M...

Detailed Description

OBJECTIVES: Primary * Determine the median time to progression in patients with unresectable primary hepatic malignancy treated with hepatic arterial infusion comprising floxuridine and dexamethason...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (ICC)
  • Peripheral, cholangiolar, or cholangiocellular types
  • Mixed HCC/ICC disease allowed
  • Unresectable disease
  • Less than 70% liver involvement
  • Radiographically bidimensionally measurable disease, defined as lesion ≥ 2 cm in the greatest diameter
  • May have failed prior systemic chemotherapy or ablative therapy
  • No radiographic evidence of esophageal varices
  • No history of variceal hemorrhage
  • No occlusion of the main portal vein or the right and left portal branches
  • No clinical ascites
  • Patients ineligible for first-line MSKCC protocols for HCC are eligible for this study provided there is no clinical or radiographic evidence of extrahepatic disease
  • No metastatic disease, including CNS metastases
  • PATIENT CHARACTERISTICS:
  • Life expectancy ≥ 12 weeks
  • Karnofsky performance status 60-100%
  • Considered a candidate for general anesthesia and hepatic artery pump placement
  • Platelet count \> 100,000/mm³
  • Albumin \> 2.5 g/dL
  • Bilirubin \< 1.8 mg/dL
  • WBC \> 3,500/mm³
  • PTT \< 1.5 times upper limit of normal
  • INR \< 1.5 OR in-range INR (usually 2.0-3.0) for patients on a stable dose of therapeutic warfarin
  • Urine protein \< 1+ by dipstick or urine analysis OR urine protein:creatinine ratio \< 1.0
  • If proteinuria ≥ 2+ at baseline, patient must have \< 1 g protein/24-hour collection
  • No concurrent disease or illness that would preclude study participation, including any of the following:
  • Hepatic encephalopathy
  • Sclerosing cholangitis
  • Gilbert's disease
  • Active infection
  • No known CNS disease
  • No history of allergic reactions attributed to compounds of similar chemical or biologic composition to bevacizumab
  • No psychiatric illness or social situation that would preclude study compliance
  • No abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 6 months
  • No serious or nonhealing active wound, ulcer, or bone fracture
  • No bleeding diathesis or coagulopathy
  • No clinically significant cardiovascular disease, including any of the following:
  • Uncontrolled hypertension, defined as systolic blood pressure (BP) \> 150 mm Hg or diastolic BP \> 100 mm Hg on antihypertensive medications
  • New York Heart Association class II-IV congestive heart failure
  • Vascular disease (e.g., aortic aneurysm, aortic dissection)
  • Myocardial infarction within the past 6 months
  • Symptomatic peripheral vascular disease
  • Unstable angina within the past 6 months
  • History of hypertensive crisis
  • Transient ischemic attack
  • Stroke
  • No other concurrent malignancy except localized basal cell or squamous cell skin cancer
  • Chronic hepatitis and/or cirrhosis allowed provided it is Child-Pugh class A disease
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • More than 4 weeks since prior and no other concurrent experimental therapy except on a Genentech-sponsored bevacizumab cancer study
  • More than 4 weeks since prior major surgical procedure or open biopsy
  • More than 1 week since prior minor surgical procedure (e.g., core biopsy), excluding placement of a vascular access device
  • No prior external-beam radiation therapy to the liver
  • No prior floxuridine
  • No chronic daily treatment with nonsteroidal anti-inflammatory medications known to inhibit platelet function
  • No chronic daily treatment with aspirin (\> 325 mg/day)
  • No concurrent or recent use of a thrombolytic agent
  • No concurrent major surgery

Exclusion

    Key Trial Info

    Start Date :

    May 9 2007

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    May 7 2024

    Estimated Enrollment :

    22 Patients enrolled

    Trial Details

    Trial ID

    NCT00410956

    Start Date

    May 9 2007

    End Date

    May 7 2024

    Last Update

    December 10 2024

    Active Locations (2)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (2 locations)

    1

    New York Weill Cornell Cancer Center at Cornell University

    New York, New York, United States, 10021

    2

    Memorial Sloan-Kettering Cancer Center

    New York, New York, United States, 10065