Pazopanib Hydrochloride in Treating Patients With Advanced or Progressive Malignant Pheochromocyt… (NCT01340794) | Clinical Trial Compass
TerminatedPhase 2
Pazopanib Hydrochloride in Treating Patients With Advanced or Progressive Malignant Pheochromocytoma or Paraganglioma
Stopped: Slow Accrual
United States7 participantsStarted 2011-05
Plain-language summary
This phase II trial studies how well pazopanib hydrochloride works in treating patients with advanced or progressive malignant pheochromocytoma or paraganglioma. Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking 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.
Inclusion Criteria:
* Histologically or cytologically confirmed malignant secretory or non-secretory pheochromocytoma or paraganglioma that is unresectable and deemed inappropriate for alternative local regional therapeutic approaches
* Objective evidence of tumor progression =\< 185 days prior to registration as assessed by:
* Unequivocal progression of objectively measured disease on successive appropriate imaging (e.g. computed tomography \[CT\] scan); in cases of uncertainty of tumor progression, the principal investigator of the study will be available to assist in decisions
* Measurable disease defined as:
* At least one non-nodal lesion whose longest diameter can be accurately measured as \>= 2.0 cm with chest x-ray, or as \>= 1.0 cm with CT scan, CT component of a positron emission tomography (PET)/CT, or magnetic resonance imaging (MRI); and/or
* A lymph node whose short axis must be \> 1.5 cm when assessed by CT scan (CT scan slice thickness recommended to be no greater than 5 mm)
* Note: Tumor lesions in a previously irradiated area are not considered measurable disease
* Life expectancy \> 24 weeks
* Eastern Cooperative Oncology Group (ECOG) performance status =\< 2
* Leukocytes \>= 3,000/uL
* Absolute neutrophil count \>= 1,500/uL
* Platelets \>= 100,000/uL
* Hemoglobin \>= 9 g/dL (5.6 mmol/L); transfusions not permitted =\< 7 days of registration
* Total bilirubin =\< 1.5 x institutional upper limit of normal (ULN) (except in cases of Gilbert's syndro…
What they're measuring
1
Response Rate (RR) (Complete Response [CR] or Partial Response [PR]) Using RECIST Version 1.1