The purpose of this study is to assess \[18F\] -fluciclatide as a biomarker of response to pazopanib and to evaluate the efficacy and safety of the combination of pazopanib and paclitaxel in platinum-resistant ovarian cancer patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
16
Pazopanib 800mg od for 7 days, followed by 18 weeks of combination therapy (paclitaxel 80mg/m2 weekly and pazopanib 800mg od). Following the completion of combination therapy, patients will continue on maintenance pazopanib 800mg od until disease progression.
Imperial College Healthcare NHS Trust
London, United Kingdom
Southend University Hospital NHS Foundation Trust
Southend, United Kingdom
Assessment of change in [18F]-fluciclatide retention parameters following 1 week of pazopanib treatment
Semi-quantitative standardized uptake value and fully quantitative net irreversible plasma to tumour transfer constant
Time frame: 1 week
The proportion of women who experience side effects from the combination of paclitaxel and pazopanib
Core study assessments including physical examination, vital signs, ECG, and adverse event reporting
Time frame: 12 months
The proportion of patients responding to combination paclitaxel and pazopanib
Time frame: 12 months
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