Status:
COMPLETED
Phase I Study of Bevacizumab and Sorafenib Combined With Low Dose Cyclophosphamide in Patients With Refractory Solid Tumors and Leukemia
Lead Sponsor:
St. Jude Children's Research Hospital
Conditions:
Refractory Solid Tumors
Leukemia
Eligibility:
All Genders
Up to 21 years
Phase:
PHASE1
Brief Summary
Phase I Study of Bevacizumab and Sorafenib Combined with Low Dose Cyclophosphamide in Patients with Refractory Solid Tumors and Leukemia. Patients with solid tumors (including central nervous tumors) ...
Detailed Description
Phase I Study of Bevacizumab and Sorafenib Combined with Low Dose Cyclophosphamide in Patients with Refractory Solid Tumors and Leukemia. Patients with solid tumors (including central nervous tumors) ...
Eligibility Criteria
Inclusion
- NOTE: As of May 2013, enrollment of solid tumor participants was completed. Participants with a diagnosis of leukemia continue to be enrolled.
- Diagnosis: Solid tumors, including central nervous system tumors and lymphomas, that are recurrent or refractory to standard therapy or for which there is no standard therapy. Histologic verification of diagnosis is required.
- Age: \< or = 21 years of age at the time of original diagnosis
- Life expectancy: at least 8 weeks
- Performance status: Karnofsky \> or = 50 for \> 10 years of age; Lansky \> or = 50 for children \< or = 10 years of age.
- Organ Function: Must have adequate organ and marrow function
- Prior Therapy: Patient must have fully recovered from the acute toxic effects of all prior therapy prior to enrolling on study.
- Must not have current or recent use of full-dose anticoagulants
- Must not have received medications known to inhibit platelet function or known to selectively inhibit cyclooxygenase-2 (COX-2) activity
- Bevacizumab and sorafenib should not be administered to pregnant women.
- Pregnancy tests must be obtained in girls who are \> 10 years of age or post-menarchal.
- Males or females of reproductive potential may not participate unless they have agreed to use an effective contraceptive method.
- Breast feeding should be discontinued if a mother wishes to participate in this study.
- Patients with a documented, chronic non-healing wound, ulcer, or bone fracture or history of a major surgical procedure or significant traumatic injury within 28 days prior to beginning therapy should be excluded due to preclinical evidence supporting the potential for delayed wound healing.
- Patients must not have a deep venous or arterial thrombosis (including pulmonary embolism) within the last three months prior to study entry, and must not have a known thrombophilic condition
- Patients must not have a history of myocardial infarction, severe or unstable angina, or severe peripheral vascular disease.
- Ability to understand and willingness of research participant or legal guardian/representative to give written informed consent.
Exclusion
- Body surface area \< 0.3 m2
- Presence of a known bleeding diathesis or coagulopathy
- Patients with evidence of intra-tumoral central nervous system hemorrhage. in current scans. Patients are required to have a head CT or MRI within 2 weeks prior to study enrollment.
- Patients with known hypersensitivity to other recombinant human antibodies
- Patients who have an uncontrolled infection
- Patients with recurrent or refractory leukemia will be excluded from the dose escalation component of the phase I trial.
Key Trial Info
Start Date :
November 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2013
Estimated Enrollment :
49 Patients enrolled
Trial Details
Trial ID
NCT00665990
Start Date
November 1 2007
End Date
August 1 2013
Last Update
January 9 2015
Active Locations (1)
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1
St. Jude Children's Research Hospital
Memphis, Tennessee, United States, 38105