Cervical Cancer
Conditions
Keywords
recurrent cervical cancer, stage IVB cervical cancer, stage IVA cervical cancer, cervical adenocarcinoma, cervical adenosquamous cell carcinoma, cervical squamous cell carcinoma
Brief summary
RATIONALE: Drugs used in chemotherapy, such as carboplatin and topotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of topotecan when given together with carboplatin and to see how well they work in treating patients with relapsed or metastatic cervical cancer.
Detailed description
OBJECTIVES: Primary * To determine the maximum tolerated dose of topotecan hydrochloride when administered with carboplatin in patients with relapsed or metastatic cervical cancer. (Phase I) * To determine the objective response rate in patients treated with this regimen. (Phase II) Secondary * To determine the dose-limiting toxicities of this regimen in these patients. (Phase I) * To assess the progression-free survival of patients treated with this regimen. (Phase II) * To assess the overall survival of patients treated with this regimen. (Phase II) * To assess the tolerability of this regimen in these patients. (Phase II) OUTLINE: This is a multicenter, phase I dose-escalation study of topotecan hydrochloride followed by a phase II study. Patients receive oral topotecan hydrochloride on days 1, 8, and 15 and carboplatin IV on day 1. Treatment repeats every 4 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients complete a quality-of-life questionnaire at baseline and then every 3 months thereafter. After completion of study therapy, patients are followed every 3 months for 1 year.
Interventions
DRUGcarboplatin
DRUGtopotecan hydrochloride
Sponsors
ARCAGY/ GINECO GROUP
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed cervical cancer, including the following cell types: * Squamous cell carcinoma * Adenocarcinoma * Adenosquamous cell carcinoma * Metastatic disease or in first relapse * Not curable by surgery and/or radiotherapy with or without chemotherapy * At least 1 non-irradiated measurable lesion * No CNS metastases PATIENT CHARACTERISTICS: * WHO performance status 0-2 * ANC ≥ 1,500/mm\^3 * Platelet count ≥ 100,000/mm\^3 * Transaminases ≤ 3 times upper limit of normal (ULN) (≤ 5 times ULN in the presence of liver metastases) * Total bilirubin ≤ 1.5 times ULN * Creatinine clearance ≥ 50 mL/min * Not pregnant or nursing * Fertile patients must use effective contraception * No other cancer within the past 5 years except for adequately treated basal cell or squamous cell carcinoma of the skin * No swallowing disorders or gastrointestinal disease resulting in an inability to take oral medication or a requirement for IV alimentation * No altered intestinal absorption * No peptic ulcers * No nephrostomy * Double-J catheter allowed * None of the following cardiovascular conditions within the past 6 months: * Uncontrolled hypertension * Coronary artery disease * NYHA class III or IV congestive heart failure * Ventricular arrhythmia * Unstable angina * Myocardial infarction * No infection or serious illness that would preclude study treatment * No contraindications to study treatment * No psychological, familial, sociological, or geographical condition that would preclude follow-up PRIOR CONCURRENT THERAPY: * No prior cytotoxic therapy except for chemoradiotherapy or pelvic radiotherapy * At least 6 months since prior platinum-based chemoradiotherapy * No concurrent participation in another clinical trial that could interfere with the objectives of this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maximum tolerated dose of topotecan hydrochloride (Phase I) | 3 months |
| Objective response rate (Phase II) | 3 months |
Countries
France
Outcome results
None listed