Overview
Fenretinide in Treating Patients With Cervical Neoplasia
Status:
Completed
Completed
Trial end date:
2001-05-01
2001-05-01
Target enrollment:
0
0
Participant gender:
Female
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 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
M.D. Anderson Cancer CenterCollaborator:
National Cancer Institute (NCI)Treatments:
Fenretinide
Criteria
DISEASE CHARACTERISTICS: Histologically diagnosed new or recurrent cervical intraepithelialneoplasia 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