Status:
COMPLETED
Abraxane and Avastin as Therapy for Patients With Malignant Melanoma, a Phase II Study
Lead Sponsor:
Lynn E. Spitler, MD
Collaborating Sponsors:
Celgene Corporation
Genentech, Inc.
Conditions:
Metastatic Malignant Melanoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The study is an open-label, single arm multicenter Phase II study to evaluate the safety and efficacy of the combination of Abraxane and Avastin as first-line therapy for patients with unresectable me...
Detailed Description
It has been suggested that chemotherapy administration may be synergistic with the effects of an antiangiogenic agent such as Avastin. A "Proof of Principal" of the concept of the synergistic effects ...
Eligibility Criteria
Inclusion
- Histologically confirmed, (surgically incurable or unresectable) stage III or IV metastatic malignant melanoma..
- Must be chemo naïve. Surgical adjuvant therapy with interferon, vaccines, or cytokines is permitted. Prior adjuvant therapy with chemotherapeutic agents is not allowed. Prior therapy for metastatic disease that is not chemotherapy is allowed. Must have discontinued prior allowable therapy at least 4 weeks prior to initiation of dosing.
- A minimum of 1 measurable lesion according to RECIST criteria.
- ECOG performance status of 0-1.
- Age ≥ 18 years.
- Adequate hematologic, renal and liver function as defined by laboratory values performed within 14 days prior to initiation of dosing.
- Patients must have recovered from effects of major surgery.
- Women of childbearing potential should be using an effective method of contraception. Women of childbearing potential must have a negative urine or serum pregnancy test up to 28 days prior to commencement of dosing and be practicing medically approved contraceptive precautions for at least 6 months after completion of treatment as directed by their physician.
- Men should use an effective method of contraception during treatment and for at least 6 months after completion of treatment as directed by their physician.
- Must have recovered from all prior treatment-related toxicities to NCI CTCAE (v 3.0) Grade of 0 or 1, except for toxicities not considered a safety risk such as alopecia.
- Before study entry, written informed consent must be obtained. Written informed consent must be obtained from the patient prior to performing any study-related procedures.
Exclusion
- Prior systemic therapy for metastatic disease with chemotherapy.
- Psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before trial entry.
- Major surgery or radiation therapy within 4 weeks of starting the study treatment.
- Known CNS disease.
- Previous Grade 2 or higher sensory neuropathy
- NCI CTCAE (V 3.0) grade 3 hemorrhage within 4 weeks of starting the study treatment.
- History of or known spinal cord compression, or carcinomatous meningitis, or evidence of symptomatic brain or leptomeningeal disease on screening CT or MRI scan.
- Any of the following within the 6 months prior to study drug administration: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, or pulmonary embolism.
- Ongoing cardiac dysrhythmias of NCI CTCAE Version 3.0 grade ≥ 2.
- 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
- Concurrent treatment on another clinical trial. Supportive care trials or non-treatment trials, e.g. QOL, are allowed.
- Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the subject inappropriate for entry into this study.
- Previous cancer (unless a DRS interval of at least 5 years) or concurrent malignancies at other sites with the exception of surgically cured carcinoma in-situ of the cervix and basal or squamous cell carcinoma of the skin.
- Known clinically uncontrolled infectious disease including HIV positivity or AIDS-related illness.
- Pregnant or nursing. Use of effective means of contraception (men and women) in subjects of child-bearing potential.
- New York Heart Association (NYHA) Grade II or greater congestive heart failure.
- Symptomatic peripheral vascular disease.
- Significant vascular disease (e.g. aortic aneurysm, aortic dissection).
- Evidence of bleeding diathesis or coagulopathy.
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, anticipation of need for major surgical procedure during the course of the study
- Minor surgical procedures such as fine needle aspirations or core biopsies within 7 days prior to Day 0
- Proteinuria at screening as demonstrated by 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).
- History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day 0
- Serious, non-healing wound, ulcer, or bone fracture
- Inability to comply with study and/or follow-up procedures
Key Trial Info
Start Date :
April 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2012
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00462423
Start Date
April 1 2007
End Date
January 1 2012
Last Update
January 8 2014
Active Locations (2)
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1
Northern California Melanoma Center
San Francisco, California, United States, 94117
2
The Angeles Clinic and Research Institute
Santa Monica, California, United States, 90404