Status:
COMPLETED
Bortezomib and Cetuximab in Treating Patients With Advanced Solid Tumors
Lead Sponsor:
Masonic Cancer Center, University of Minnesota
Conditions:
Breast Cancer
Colorectal Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
RATIONALE: Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Som...
Detailed Description
OBJECTIVES: Primary * To determine the maximum tolerated dose of bortezomib when given together with cetuximab in patients with advanced solid tumors expressing epidermal growth factor receptor (EGF...
Eligibility Criteria
Inclusion
- Diagnosis of solid tumor that overexpresses epidermal growth factor receptor (EGFR) including, but not limited to, the following:
- Breast cancer
- Lung cancer
- Colon cancer
- Pancreatic cancer
- Head and neck cancer
- Kidney cancer
- Sarcoma
- Advanced disease
- Must have failed or become intolerant to prior standard therapy and is no longer likely to respond to such therapy
- Measurable or nonmeasurable disease
- ECOG performance status 0-1
- ANC ≥ 1,500/mm³
- Platelet count \> 100,000/mm³
- Hemoglobin \> 9 g/dL
- Bilirubin \< 1.5 times upper limit of normal (ULN)
- Alkaline phosphatase \< 3.0 times ULN (5.0 times ULN if liver has tumor involvement)
- Aspartate aminotransferase (AST) and alanine aminotransferase (\*ALT) \< 3.0 times upper limit of normal (ULN) (5.0 times ULN if liver has tumor involvement)
- Creatinine clearance \> 30 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 3 months after completion of study treatment
- Recovered from all prior therapy
- Prior systemic chemotherapy, immunotherapy, or biological therapy allowed
- At least 14 days since prior radiotherapy or systemic therapy
- At least 30 days since prior investigational agents
- At least 14 days since other prior investigational drugs (for reasons other than the treatment of cancer)
Exclusion
- Untreated or symptomatic central nervous system (CNS) metastases
- Concurrent serious systemic disorders (e.g., active infection) that, in the opinion of the investigator, would compromise the safety of the patient or compromise the patient's ability to complete the study
- Uncontrolled diabetes
- Myocardial infarction within the past 6 months
- New York Heart Association (NYHA) class III or IV heart failure
- Uncontrolled angina
- Severe uncontrolled ventricular arrhythmias
- Evidence of acute ischemia or active conduction system abnormalities by ECG
- Peripheral neuropathy Common Terminology Criteria for Adverse Events (CTCAE) grade \> 2
- Known hypersensitivity to bortezomib, boron, or mannitol
- Serious medical or psychiatric illness likely to interfere with study participation
- Prior bortezomib and/or cetuximab
- Concurrent filgrastim (G-CSF) or other hematologic support during course 1 of study treatment
Key Trial Info
Start Date :
November 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2010
Estimated Enrollment :
37 Patients enrolled
Trial Details
Trial ID
NCT00622674
Start Date
November 1 2005
End Date
February 1 2010
Last Update
December 2 2017
Active Locations (1)
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1
Masonic Cancer Center at University of Minnesota
Minneapolis, Minnesota, United States, 55455