Pilot Study of IV and IP Chemotherapy Plus Abdominal Hyperthermia for Ovarian Ca

NCT ID: NCT00787488

Last Updated: 2014-11-11

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-04-30
• Study Completion Date: 2009-04-30

Brief Summary

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.

Detailed Description

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.

Conditions

Ovarian Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Chemotherapy plus Hyperthermia

Group Type: EXPERIMENTAL

Hyperthermia

Intervention Type: DEVICE

Every 3 weeks

Interventions

Hyperthermia

Every 3 weeks

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Histologically diagnosed Stage III or Stage IV advanced, persistent, or recurrent epithelial ovarian, primary peritoneal, or fallopian tube cancer
• Optimal debulking (< 1cm residual disease) of their disease within 6 weeks of the start of the study
• Patients must have received no more than 2 prior chemotherapy regimens with at least 4 weeks since prior chemotherapy
• GOG performance status 0, 1, or 2
• Patients must have normal organ and marrow function defined as:
• absolute neutrophil count >1,500/mcL
• platelets >100,000/mcL
• total bilirubin and creatinine <1.5 X institutional upper limit of normal(ULN)
• AST(SGOT)/ALT(SGPT)<3 X institutional ULN

Exclusion Criteria

• Patients with biochemical recurrences or evidence of measurable disease
• Patients with suboptimal (>1 cm) residual disease
• Patients who have had chemotherapy within 4 weeks prior
• Receiving any investigational agents
• Known brain metastases
• Epithelial ovarian carcinoma of low malignant potential (borderline carcinomas)
• Uncontrolled intercurrent illness
• Prior radiation therapy
• History of other invasive or pre-invasive malignancies (except non-melanoma skin cancer) within the past 5 years

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 72 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Mark Dewhirst

OTHER

Sponsor Role: lead

Responsible Party

Mark Dewhirst

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Elizabeth Jewell, MD

Role: PRINCIPAL_INVESTIGATOR

Duke University

Angeles Secord, MD

Role: PRINCIPAL_INVESTIGATOR

Duke University

Ellen Jones, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Duke University Medical Center, Radiation Oncology

Other Identifiers

Pro00008510

Identifier Type: -

Identifier Source: org_study_id