Overview

Paclitaxel, Cisplatin, and Topotecan With or Without Filgrastim in Treating Patients With Newly Diagnosed Stage III or Stage IV Epithelial Ovarian Cancer

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
Female
Summary
Phase I trial to study the effectiveness of paclitaxel, cisplatin, and topotecan with or without filgrastim in treating patients who have newly diagnosed stage III or stage IV epithelial ovarian cancer. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Colony-stimulating factors such as filgrastim may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of chemotherapy
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Cancer Institute (NCI)
Treatments:
Albumin-Bound Paclitaxel
Cisplatin
Lenograstim
Paclitaxel
Topotecan
Criteria
Inclusion Criteria:

- Histologically confirmed epithelial ovarian carcinoma

- No borderline ovarian carcinoma

- Stage III/IV disease that has been suboptimally or optimally debulked

- The following histologies are eligible:

- Adenocarcinoma (unspecified)

- Mucinous cystadenocarcinoma

- Clear cell adenocarcinoma

- Serous cystadenocarcinoma

- Endometrioid adenocarcinoma

- Transitional cell carcinoma

- Malignant Brenner's tumor

- Undifferentiated carcinoma

- Mixed epithelial carcinoma

- Extraovarian papillary serous cystadenocarcinoma

- Measurable or evaluable disease

- Performance status - GOG 0-1

- Enabling completion of at least 2 courses of therapy

- Absolute neutrophil count at least 1,500/mm^3

- Platelet count at least 100,000/mm^3

- Bilirubin no greater than 1.5 mg/dL

- Creatinine clearance at least 60 mL/min

- No myocardial infarction within 6 months

- No congestive heart failure

- No unstable or uncontrolled angina

- No history of cardiac arrhythmia requiring anti-arrhythmia medication

- No uncontrolled hypertension

- No hypersensitivity to E. coli-derived drug preparation

- No active infection

- No sensory neuropathy

- No other malignancies within the past 5 years except nonmelanomatous skin cancer

- No prior chemotherapy

- No prior radiotherapy

- Recovered from any recent surgery