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Clinical Trials/NCT00466687
NCT00466687
Completed
Phase 2

A Phase II Trial of Tarceva (Erlotinib) and Avastin (Bevacizumab) in the Treatment of Patients With Metastatic Melanoma

Vanderbilt-Ingram Cancer Center4 sites in 1 country34 target enrollmentSeptember 2004

Overview

Phase
Phase 2
Intervention
bevacizumab
Conditions
Melanoma
Sponsor
Vanderbilt-Ingram Cancer Center
Enrollment
34
Locations
4
Primary Endpoint
Number of Patients With Response
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving erlotinib together with bevacizumab may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving erlotinib together with bevacizumab works in treating patients with stage IV melanoma.

Detailed Description

OBJECTIVES: Primary * Determine the overall response rate, response duration, and frequency of progression-free survival at 6 months in patients with stage IV melanoma treated with erlotinib hydrochloride and bevacizumab. * Determine objective responses in patients treated with this regimen. Secondary * Determine the overall safety and tolerability of this regimen in these patients. * Evaluate tissue blocks for EGFR by monoclonal antibody H11 (DAKO) or fluorescence in situ hybridization(FISH)7p12-specific probe-overexpression or amplification in patients treated with this regimen. OUTLINE: This is a multicenter study. Patients receive oral erlotinib hydrochloride once daily on days 1-28 and bevacizumab IV over 30-90 minutes on days 1 and 15. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo tissue collection to analyze EGFR by monoclonal antibody H11 (DAKO) or fluorescence in situ hybridization (FISH) 7p12-specific probe-overexpression or amplification. Biological markers AKT, MAPK, p27, p21, CD13, CD34, and factor VIII are also measured. After completion of study treatment, patients are followed periodically.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
September 2008
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jeffrey A. Sosman, MD

Professor of Medicine; Director, Melanoma and Tumor Immunotherapy

Vanderbilt-Ingram Cancer Center

Eligibility Criteria

Inclusion Criteria

  • Measurable Stage IV melanoma
  • Easter Cooperative Oncology Group (ECOG) Performance Status must be 0-1
  • Good organ function as demonstrated by, Creatinine \<2.mg/dl, AST or ALT \<5 times upper limit of normal for subjects with documented liver metastases; \<2.5 times the upper limit of normal (ULN) for subjects without evidence of liver metastases, bilirubin\<2.0mg/dl,, absolute neutrophil count (ANC)\>1500/ul, platelets\>75k/ul, hemoglobin (Hgb)\>9 (may be transfused to obtain)
  • Prior therapy: adjuvant interferon (IFN) allowed; no more than one prior regimen for advanced stage IV disease
  • Patients must have a life expectancy of \>3 months
  • Patients with brain metastases are eligible only if they fulfill the following: resected or stereotactic treatment a minimum of 3 months previously and no active CNS disease since then; brain metastases treated greater than 6 months ago without evidence of progression or hemorrhage, \<1cm in size per lesion (up to 3 lesions), and off all steroids
  • Patients may not have received other agents, either investigational or marketed, which act by either EGFr inhibition or anti-angiogenesis mechanisms. Other epidermal growth factor receptor (EGFR) inhibitors include (but are not limited to): Iressa, erbitux, CI-
  • Angiogenesis inhibitors include (but are not limited to): SU5416, SU6668, SU 0122348, CP547632, VEGF Trap, anti-integrin αVβ
  • Recovered from toxicity of major surgery (4 wks), chemotherapy or biologic therapy (4 wks), and/or radiation therapy (2 wks)
  • No active other malignancy within 12 months

Exclusion Criteria

  • Subjects meeting any of the following criteria (3.2.2-3.2.16) are ineligible for study entry
  • Compromised renal or hepatic function as defined by Creatinine \>2.0mg/dl, aspartate transaminase (AST) or alanine transaminase (ALT) \>5 times upper limit of normal for subjects with documented liver metastases; \>2.5 times the upper limit of normal (ULN) for subjects without evidence of liver metastases
  • Patient may not be part of any other investigational studies
  • internationalized normal ratio (INR) \> 1.5
  • Patients with PEG or G-tube are ineligible.
  • Major surgical procedure, open biopsy; or significant traumatic injury within 28 days, or anticipation of need for major surgical procedure during the course of the study
  • Any non-healing wound, ulcer, or bone fracture.
  • Any clinical evidence or history of a bleeding diathesis or coagulopathy.
  • Patients with a history of deep vein thrombosis or thromboembolic disease within the past 6 months.
  • History of acute myocardial infarction within 6 months. In addition, patients are ineligible if they have clinically significant cardiovascular disease ((e.g., uncontrolled hypertension \[blood pressure of \>160/110 mmHg on medication\], New York Heart Association (NYHA) Grade II or greater congestive heart failure, serious cardiac dysrhythmia requiring medication, or peripheral vascular disease (Grade II or greater)

Arms & Interventions

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: bevacizumab

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: erlotinib hydrochloride

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: fluorescence in situ hybridization

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: gene expression analysis

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: immunologic technique

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: laboratory biomarker analysis

Therapeutic Intervention

Tarceva and Avastin: * Tarceva: 150mg PO, days 1-28 * Avastin: 10mg/kg, IV infusion, days 1,15 Regimen will be repeated every 28 days = 1 course

Intervention: biopsy

Outcomes

Primary Outcomes

Number of Patients With Response

Time Frame: At 6 months

Per Response Evaluation Criteria in Solid Tumor (RECIST): Progressive disease (PD): \>=20% increase in sum of longest diameter (LD) of target lesion(s), taking as reference smallest sum LD recorded since treatment started. Complete response (CR): disappearance of all target lesions. Partial response (PR): \>=30% decrease in sum of LD of target lesion(s), taking as reference baseline sum LD. Stable disease (SD): neither sufficient shrinkage to qualify as PR nor sufficient increase to qualify as PD.

Secondary Outcomes

  • Time to Disease Progression.(up to one year after off-study date)
  • Progression-free Survival at 6 Months(6 months)
  • Number of Patients With Each Worst-grade Toxicity Response(Day 1 of each 28-day cycle for 6 cycles (168 days))

Study Sites (4)

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