Overview

Radiation Therapy With or Without Cisplatin or Fluorouracil in Treating Patients With Cancer of the Cervix

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
Female
Summary
RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining radiation therapy and chemotherapy may kill more tumor cells. It is not known whether receiving radiation therapy plus cisplatin is more effective than receiving radiation therapy plus fluorouracil in treating patients with cancer of the cervix. PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy plus cisplatin or fluorouracil in treating patients with primary stage IIB, stage IIIB, or stage IVA cancer of the cervix.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Gynecologic Oncology Group
Collaborator:
National Cancer Institute (NCI)
Treatments:
Cisplatin
Fluorouracil
Criteria
DISEASE CHARACTERISTICS: Primary, previously untreated, histologically confirmed invasive
squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma of the uterine cervix
stage IIB, IIIB, or IVA Negative para-aortic lymph nodes determined by lymphangiogram, CT,
MRI, or lymphadenectomy (excluding suspicious para-aortic lymph nodes) Para-aortic
lymphadenectomy must be performed extraperitoneally or by laparoscopy No histologically
confirmed cancer involving the para-aortic lymph nodes, intraperitoneal disease, or
positive peritoneal cytology No recurrent invasive carcinoma of the uterine cervix,
regardless of previous treatment or cervix cancers other than squamous cell, adenosquamous,
or adenocarcinoma No carcinoma of the cervical stump

PATIENT CHARACTERISTICS: Age: Any age Performance status: GOG 0-3 Life expectancy: Not
specified Hematopoietic: WBC at least 3,000/mm3 Platelet count at least 100,000/mm3
Hepatic: Bilirubin no greater than 1.5 times normal SGOT and alkaline phosphatase no
greater than 3 times normal Renal: Creatinine no greater than 2.0 mg/dL Other: No
septicemia or severe infection Not pregnant Negative pregnancy test Effective contraception
required of fertile patients No other invasive malignancy unless disease free for at least
5 years and no prior cancer treatment that contraindicated this protocol therapy No
concomitant malignancy other than nonmelanomatous skin cancer Must complete smoking history
questionnaire and provide urine specimen for cotinine analysis

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior cytotoxic
chemotherapy Endocrine therapy: Not specified Radiotherapy: No prior radiation therapy to
the pelvis Surgery: No prior hysterectomy