Overview

Fenretinide in Treating Patients With Cervical Neoplasia

Status:
Completed
Trial end date:
2001-05-01
Target enrollment:
0
Participant gender:
Female
Summary
RATIONALE: Chemoprevention uses drugs to try and prevent development of cancer. Fenretinide may be effective in treating cervical neoplasia and preventing cervical cancer. PURPOSE: Randomized double-blinded phase III trial to compare the effectiveness of fenretinide to placebo in treating patients with cervical neoplasia.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Fenretinide
Criteria
DISEASE CHARACTERISTICS: Histologically diagnosed new or recurrent cervical intraepithelial
neoplasia grade 2-3 lesion involving at least one quadrant of the transformation zone of
the cervix

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Zubrod 0-2 Life expectancy:
At least 12 months Hematopoietic: Absolute granulocyte count greater than 1500/mm3 Platelet
count greater than 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 mg/dL Renal:
Creatinine no greater than 1.5 mg/dL Other: Fertile patients must use effective
contraception Fasting triglyceride less than 2 times normal No prior malignancy Must
consent to colposcopy and cervical biopsy

PRIOR CONCURRENT THERAPY: Not specified