Status:
WITHDRAWN
Study of Cetuximab and Bevacizumab in Cancer of the Esophagus After Failure of Patient's First Therapy
Lead Sponsor:
Emory University
Collaborating Sponsors:
Genentech, Inc.
Conditions:
Esophageal Carcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to test the drug bevacizumab in combination with cetuximab. Because this combination has not been tested in cancer patients before, results will be analyzed to see what ef...
Detailed Description
Cancer of the esophagus often has a poor outcome since many patients have advanced disease when they are diagnosed. The average survival rate after five years has increased from 4% in the 1970s to aro...
Eligibility Criteria
Inclusion
- Patients must have histologically or cytologically confirmed squamous cell carcinoma or esophageal adenocarcinoma.
- The disease must be recurrent after first line systemic therapy, with or without radiation, with or without surgery.
- Patients must be at least 1 month from prior chemotherapy or radiation therapy.
- ECOG performance status ≤ 1 (Karnofsky \> 60%)
- Life expectancy of greater than 12 weeks.
- Age \> 18.
- Patients must have normal bone marrow and other organ function or defined below:
- Absolute neutrophil count, \> 1, 500/μL
- Platelet counts, \> 100, 00/μL
- \_ Hemoglobin, \> 8.0 gm/dL-
- Creatinine(\< 1.5mg/dL)
- No significant intercurrent medical illness (including NYHA class II, III or IV heart disease, significant arrhythmias requiring medication, symptomatic coronary artery disease, myocardial infarction within the previous 6 months.
- Women of childbearing potential must have a negative pregnancy test.
- Ability to understand and willingness to sign a written informed consent document.
Exclusion
- I. Disease-specific Exclusions
- All histologic types other than squamous cell carcinoma or adenocarcinoma.
- Patients currently receiving other investigational agents, or who have received cetuximab previously.
- Patients with known brain metastases.
- History of severe allergic reactions attributed to compounds of similar chemical or biologic composition to Cetuximab or Bevacizumab.
- Patients with history of any other malignancy (except non-melanomatous skin cancer or CIS of cervix) are ineligible unless a period of 5 years has lapsed since treatment of the previous cancer and the patient has remained continuously disease free.
- Patients who are felt to be poorly compliant.
- Women who are breast-feeding.
- II. General Medical Exclusions
- Subjects meeting any of the following criteria are ineligible for study entry:
- Inability to comply with study and/or follow-up procedures.
- Life expectancy of less than 12 weeks.
- Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study other than a Genentech-sponsored bevacizumab cancer study.
- III. Bevacizumab-Specific Exclusions
- Inadequately controlled hypertension (defined as systolic blood pressure \>150 and/or diastolic blood pressure \>100 mmHg on antihypertensive medications).
- Any prior history of hypertensive crisis or hypertensive encephalopathy.
- New York Heart Association (NYHA) Grade II or greater congestive heart failure
- History of myocardial infarction or unstable angina within 6 months prior to study enrollment.
- History of stroke or transient ischemic attack within 6 months prior to study enrollment.
- Known CNS disease.
- Significant vascular disease (e.g., aortic aneurysm, aortic dissection).
- Symptomatic peripheral vascular disease.
- Evidence of bleeding diathesis or coagulopathy.
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to study enrollment or anticipation of need for major surgical procedure during the course of the study.
- Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to study enrollment.
- History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to study enrollment.
- Serious, non-healing wound, ulcer, or bone fracture.
- Proteinuria at screening as demonstrated by either
- Urine protein: creatinine (UPC) ratio ≥ 1.0 at screening OR
- Urine dipstick for proteinuria ≥ 2+ (patients discovered to have ≥ 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour urine collection and must demonstrate ≤ 1g of protein in 24 hours to be eligible)
- Known hypersensitivity to any component of bevacizumab.
- Pregnant (positive pregnancy test) or lactating. Use of effective means of contraception (men and women) in subjects of child-bearing potential.
- History of myocardial infarction or unstable angina within 6 months of study enrollment.
Key Trial Info
Start Date :
October 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00636298
Start Date
October 1 2008
End Date
March 1 2012
Last Update
November 19 2013
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