Ovarian Cancer Clinical Trial
Official title:
A Pilot Study of Intravenous and Intraperitoneal Chemotherapy Plus Abdominal Hyperthermia to Treat Optimally Debulked and Recurrent Epithelial Ovarian, Fallopian Tube, and Primary Peritoneal Cancers
This is a pilot study aimed to test the feasibility and safety of administering combination chemotherapy with paclitaxel (both intravenously and intraperitoneally) and cisplatin (intraperitoneally) plus whole abdominal hyperthermia every 3 weeks in the treatment of optimally debulked, advanced or recurrent ovarian, primary peritoneal, and fallopian tube cancer patients.
Day 1 of each 21 day Cycle:
Paclitaxel 175 mg/m2 IV (infused over 3 hours)
Day 1 or 2 of each Cycle Adequate IV hydration with normal saline (1000 ml
recommended)followed by intraperitoneal infusion of 500 ml normal saline through the IP
port.
Cisplatin 75 mg/m2 reconstituted in 500 ml NS warmed to 37 degrees Celsius is infused IP (30
minute infusion)followed immediately by whole abdominal hyperthermia
Abdominal hyperthermia will be delivered using the BSD 2000 ellipse system to target
temperatures of 40-42 degrees Celsius monitored via rectally and vaginally continuing for no
greater than 60 minutes after maximal 30 minute warm-up phase. Total duration of
hyperthermia will be no greater than 90 minutes.
Day 8:
Paclitaxel 60 mg/m2 IP. Paclitaxel will be diluted and filtered initially in 1000 ml of
normal saline or D5W warmed to 37 degrees Celsius. For IP administration, the patient must
receive an additional 1000 ml of normal saline degrees Celsius in the peritoneal cavity.
Cycles will be repeated every 3 weeks x 6 cycles. Patients will be followed until disease
progression/recurrence or death.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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