SU5416 in Treating Patients With Malignant Mesothelioma (NCT00006014) | Clinical Trial Compass
CompletedPhase 2
SU5416 in Treating Patients With Malignant Mesothelioma
United States45 participantsStarted 2000-08
Plain-language summary
Phase II trial to study the effectiveness of SU5416 in treating patients who have malignant mesothelioma. SU5416 may stop the growth of malignant mesothelioma by stopping blood flow to the tumor.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
DISEASE CHARACTERISTICS:
* Histologically or cytologically proven malignant mesothelioma (epithelial, sarcomatoid, or mixed subtype) that is not amenable to surgery or radiotherapy
* Measurable disease
* At least 20 mm by conventional techniques or at least 10 mm by spiral CT scan
* Pleural effusions and ascites are not considered measurable lesions
* Only site of measurable disease must not be located within prior radiotherapy port
* Lesion must be accessible for biopsy
* History of previously treated CNS metastasis allowed if:
* Neurologically stable
* No requirement for IV or oral steroids or IV anticonvulsants
* No active or residual disease by brain CT or MRI scan
* Patients with neurologic signs or symptoms suggestive of CNS metastasis must have a negative brain CT or MRI scan
PATIENT CHARACTERISTICS:
* Age: 18 and over
* Performance status: WHO 0-2
* Life expectancy: At least 12 weeks
* WBC at least 3,000/mm3
* Platelet count at least 75,000/mm3
* Bilirubin no greater than 1.5 mg/dL
* SGOT and SGPT no greater than 2.5 times upper limit of normal
* Creatinine no greater than 1.5 mg/dL OR creatinine clearance at least 60 mL/min
* No uncompensated coronary artery disease on electrocardiogram or physical examination
* No history of myocardial infarction or severe/unstable angina within the past 6 months
* No severe peripheral vascular disease associated with diabetes mellitus
* No deep vein or arterial thrombosis within the past 3 months
* No pulmonary embolism wā¦