Bevacizumab in Treating Patients With Unresectable Nonmetastatic Liver Cancer

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2

Conditions: Recurrent Adult Primary Liver Cancer; Localized Unresectable Adult Primary Liver Cancer; Adult Primary Hepatocellular Carcinoma

Treatments: Biological: bevacizumab

Study type: Interventional

Funder types: NIH

Identifiers

NCT00055692

P30CA013330 (U.S. NIH Grant/Contract)

5611 (Other Identifier)

NCI-2012-02518 (Other Identifier)

NCI-5611 (Other Identifier)

N01CM62203 (U.S. NIH Grant/Contract)

N01CM62204 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This phase II trial is to see if bevacizumab works in treating patients who have unresectable nonmetastatic liver cancer that has not spread to the main portal vein. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them.

Full description

OBJECTIVES:

I. Determine the efficacy of bevacizumab, in terms of progression-free survival and disease stability and response, in patients with unresectable nonmetastatic hepatocellular cancer (HCC) without main portal vein invasion.

II. Determine the safety of this drug in these patients. III. Assess tumor vascular perfusion kinetics, by dynamic gadolinium-enhanced MRI, in patients before and after treatment with this regimen.

IV. Determine the effect of vascular endothelial growth factor (VEGF)-inhibition by this drug on circulating levels of VEGF and related cytokines that also contribute to HCC pathogenesis (including bFGF, TGF-alpha, and IGF-II) and on potential alterations of these levels on prognostic variables in these patients.

V. Determine the effect of VEGF-inhibition by this drug on hepatic function and hepatitis viral activity in cirrhosis in these patients.

OUTLINE: This is a multicenter, pilot study.

Patients receive bevacizumab IV over 30-90 minutes on day 1. Treatment continues every 2 weeks in the absence of disease progression or unacceptable toxicity.

PROJECTED ACCRUAL: A total of 18-46 patients will be accrued for this study.

Enrollment: 46 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed hepatocellular carcinoma

  • Confirmed by needle aspirate, biopsy, or prior surgical resection specimen

• Clinically confirmed hepatocellular carcinoma defined as follows:

  • Cirrhosis or chronic hepatitis B or C virus infection, with 1 or more hypervascular liver masses more than 2 cm
  • Alpha-fetoprotein (AFP) greater than 400 ng/mL OR greater than 3 times normal and doubling in value during the past 3 months

• Deemed unresectable

  • Prior surgical resection allowed
  • Recurrence after hepatic resection or other procedure allowed
  • Tumor that extends into branches of the portal or hepatic veins allowed
  • No tumor invading the main portal vein (portal trunk) or inferior vena cava
  • No tumor occupying more than 50% of the liver volume

• Enlargement/involvement of regional lymph nodes allowed

• At least 1 unidimensionally measurable lesion at least 20 mm

  • No poorly defined lesions
  • No vague hypervascular patches

• Child-Pugh class A or compensated Child-Pugh class B liver dysfunction

  • No Child-Pugh class C or uncompensated class B indicated by active encephalopathy, persistent ascites, or prothrombin time greater than 1.5 times normal
  • Prior ascites allowed if manageable with diuretics alone
  • No repeated paracentesis (more than 1 per month)

• No extrahepatic metastasis

• No documented brain metastases

• No history or clinical evidence of CNS disease (e.g., primary brain tumor, seizures uncontrolled with standard medical therapy, or history of stroke)

• Performance status - ECOG 0-2

• Absolute neutrophil count greater than 1,500/mm^3

• Hemoglobin at least 8 g/dL

• Platelet count at least 75,000/mm^3

• No prior serious bleeding event (unrelated to liver disease)

• No bleeding diathesis

• No coagulopathy

• Bilirubin no greater than 3 mg/dL

• Transaminases less than 5 times upper limit of normal (ULN)

• Albumin at least 2.5 mg/dL

• PTT less than 4 seconds above ULN

• INR less than 1.5 (for patients receiving warfarin)

• Creatinine less than 1.5 g/dL

• Urine protein less than 500 mg/24hrs*

Exclusion criteria

• No thromboembolic event within the past 12 months
• No clinically significant cardiovascular disease
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No active infection requiring parenteral antibiotics
• No serious non-healing wound/ulcer or bone fracture
• No variceal bleeding within the past 6 months
• No malignancy within the past 5 years except localized nonmelanoma skin cancer
• No ongoing psychiatric or social situation that would preclude study compliance
• No known hypersensitivity to Chinese hamster ovary cell products
• No known hypersensitivity to other recombinant human antibodies
• No more than 1 prior biologic therapy
• No concurrent interferon
• No concurrent interleukin-2
• No more than 1 prior antineoplastic chemotherapy
• At least 4 weeks since prior invasive surgery, including open biopsy
• At least 2 weeks since prior needle biopsy (core or fine-needle aspirate)
• No concurrent hepatic transplant
• At least 4 weeks since prior anticancer therapy
• No concurrent platelet-stimulating factors (e.g., oprelvekin)
• No concurrent full-dose anticoagulants or thrombolytic agents (except as required to maintain patency of pre-existing, permanent indwelling IV catheters)
• No chronic daily antiplatelet drugs (e.g., aspirin doses of 325 mg/day or higher or non-steroidal anti-inflammatory drugs)

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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46 participants in 1 patient group

Treatment (bevacizumab)

Experimental group

Description:

Patients receive bevacizumab IV over 30-90 minutes on day 1. Treatment continues every 2 weeks in the absence of disease progression or unacceptable toxicity.

Treatment:

Biological: bevacizumab