Vandetanib and Bevacizumab in Treating Patients With Advanced Solid Tumors or Lymphoma

March 14, 2012 updated by: National Institutes of Health Clinical Center (CC)

Phase I Study of Vandetanib (ZD 6474) and Bevacizumab Combination Therapy Evaluating the VEGF and EGF Signal Transduction Pathways in Adults With Solid Tumors and Lymphomas

RATIONALE: Vandetanib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. 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 carry cancer-killing substances to them. Bevacizumab and vandetanib may also stop the growth of cancer cells by blocking blood flow to the cancer. Giving vandetanib together with bevacizumab may kill more cancer cells.

PURPOSE: This phase I trial is studying the side effects and best dose of vandetanib and bevacizumab in treating patients with advanced solid tumors or lymphoma.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

OBJECTIVES:

Primary

  • Determine the maximum tolerated dose, safety, and toxicity of vandetanib and bevacizumab in patients with advanced solid tumors or lymphoma.

Secondary

  • Characterize the pharmacokinetic profile of this regimen in these patients.
  • Measure changes in VEGF and other angiogenic cytokines in plasma samples from these patients.
  • Determine the biochemical changes in the EGF signal transduction pathways in tumor biopsy samples from these patients.
  • Determine the anti-angiogenic effects of this regimen in tumor biopsy samples from these patients.
  • Evaluate the application of dynamic contrast-enhanced MRI to determine early changes in tumor vascular permeability during treatment.
  • Evaluate the effects of this regimen on circulating endothelial progenitors and mature circulating endothelial cells in these patients.

OUTLINE: Patients receive oral vandetanib once daily on days 1-21 and bevacizumab IV over 30-90 minutes on day 1. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.

Patients undergo blood sample collection periodically for correlative laboratory studies, including pharmacokinetic, biomarker (VEGF and other angiogenic cytokines), and circulating endothelial cell analysis. Patients may also undergo optional tumor biopsies for additional correlative laboratory studies.

Study Type

Interventional

Enrollment (Anticipated)

18

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Maryland
      • Bethesda, Maryland, United States, 20892-1182
        • Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

DISEASE CHARACTERISTICS:

  • Histologically confirmed advanced malignancy, including the following:

    • Solid tumor that is refractory to standard therapy or for which no standard therapy exists

      • No lung carcinoma of squamous cell or small cell histology (mixed tumors will be categorized by the predominant cell type)

        • Histological confirmation based on sputum cytology alone is not acceptable
    • Lymphoma (Hodgkin or non-Hodgkin lymphoma) that has progressed after standard therapy AND for which stem cell transplantation is not indicated or has been refused

  • No known CNS disease, except for treated brain metastasis meeting the following criteria:

    • No ongoing requirement for steroids

    • No evidence of progression or hemorrhage by clinical examination and brain imaging (MRI or CT scan) for ≥ 3 months after treatment

      • Stable dose of anticonvulsants allowed

    • Prior treatment for brain metastases may have included whole-brain radiotherapy, radiosurgery (gamma knife, linear accelerator, or equivalent), or a combination of therapy as deemed appropriate by the treating physician

      • Neurosurgical resection or brain biopsy for treatment of CNS metastases allowed provided treatment was completed more than 3 months ago

PATIENT CHARACTERISTICS:

  • ECOG performance status (PS) 0-2 OR Karnofsky PS 60-100%
  • Life expectancy > 3 months
  • Absolute neutrophil count ≥ 1,500/μL
  • Platelet count ≥ 100,000/μL
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • AST and ALT ≤ 2.5 times ULN
  • Creatinine < 1.5 times ULN OR creatinine clearance ≥ 60 mL/min
  • Urine protein:creatinine ratio ≤ 0.5 OR urine protein < 1,000 mg by 24-hour urine collection
  • Activated partial thromboplastin time ≤ 1.5 times ULN
  • Prothrombin time OR INR < 1.5 times ULN
  • Potassium between 4 mmol/L and ULN (supplementation allowed)
  • Magnesium normal (supplementation allowed)
  • Serum calcium (adjusted for albumin) or ionized calcium normal (supplementation allowed)
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for ≥ 6 months after completion of study therapy

  • HIV-positivity allowed provided the following criteria are met:

    • Patient does not require anti-HIV therapy
    • CD4 count > 350/mm^3
    • HIV viral load < 25,000 copies/mm^3
    • No history of opportunistic infections

  • No evidence of severe or uncontrolled systemic disease or any concurrent condition that could compromise participation in the study, including any of the following:

    • Active or uncontrolled infection
    • Immune deficiencies
    • HIV infection requiring anti-HIV therapy
    • Hepatitis B
    • Hepatitis C
    • Uncontrolled diabetes
    • Uncontrolled hypertension
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • Myocardial infarction within the past 6 months
    • Uncontrolled cardiac arrhythmia
    • Stroke/cerebrovascular accident within the past 6 months
    • Psychiatric illness/social situation that, in the investigator's opinion, would make it undesirable for the patient to participate in the study or that would jeopardize study compliance
  • No New York Heart Association class III or IV heart disease within the past 6 months

  • No history of arrhythmia (i.e., multifocal premature ventricular contractions, bigeminy, trigeminy, ventricular tachycardia, or uncontrolled atrial fibrillation) that is symptomatic or requires treatment

    • Atrial fibrillation allowed provided it is controlled with medication
  • No asymptomatic sustained ventricular tachycardia
  • No other cardiac disease that, in the investigator's opinion, would increase the risk of ventricular arrhythmia
  • QTc < 480 msec (with measurable Bazett correction) by screening ECG
  • No history of QTc prolongation as a result of other medications that required discontinuation
  • No congenital long QT syndrome
  • No first-degree relative with unexplained sudden death at under 40 years of age
  • No left bundle branch block
  • No hypertension not controlled by medical therapy, defined as systolic blood pressure > 150 mm Hg or diastolic blood pressure > 90 mm Hg despite optimal medical management
  • No other clinically significant cardiac event
  • No thromboembolic disease within the past 6 months
  • No significant vascular disease (e.g., aortic aneurysm or aortic dissection) or clinically significant peripheral vascular disease
  • No serious non-healing wounds (including wounds healing by secondary intention)
  • No acute or non-healing ulcers
  • No bone fractures within the past 3 months
  • No abdominal fistula, gastointestinal perforation, or intra-abdominal abscess within the past 28 days
  • No currently active diarrhea that may affect the ability of the patient to absorb or tolerate vandetanib
  • No hemoptysis (bright red blood of ≥ ½ teaspoon per episode) within the past 3 months
  • No known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • Prior anti-VEGF therapy allowed
  • More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin C) or radiotherapy and recovered
  • More than 4 weeks since prior major surgery and recovered
  • At least 2 weeks since prior investigational drugs given in a phase 0 clinical trial
  • More than 10 days since prior and no concurrent aspirin (> 325 mg/day) or chronic use of other NSAIDs
  • No concurrent regular, therapeutic anticoagulation

  • No concurrent medication that may cause QTc prolongation, induce Torsades de Pointes, or induce CYP3A4 function, including any of the following:

    • Rifampin
    • Rifabutin
    • Phenytoin
    • Carbamazepine
    • Phenobarbital
    • Hypericum perforatum (St. John's wort)
  • No other concurrent antineoplastic therapy, except for gonadotropin-releasing hormone therapy for prostate cancer

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Toxicity
Safety
Maximum tolerated dose

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Institutes of Health Clinical Center (CC)

Collaborators

National Cancer Institute (NCI)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2008

Primary Completion (ACTUAL)

June 1, 2010

Study Completion (ACTUAL)

February 1, 2011

Study Registration Dates

First Submitted

August 13, 2008

First Submitted That Met QC Criteria

August 13, 2008

First Posted (ESTIMATE)

August 14, 2008

Study Record Updates

Last Update Posted (ESTIMATE)

March 16, 2012

Last Update Submitted That Met QC Criteria

March 14, 2012

Last Verified

March 1, 2012

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 080087
  • 08-C-0087
  • NCI-P7189
  • CDR0000590152

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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