A Phase II Trial of Gemzar (Gemcitabine), Taxol (Paclitaxel), and Platinol (Cisplatin) (GTP) in Treatment of Advanced Transitional Cell Carcinoma of the Urothelium
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Enrollment
- 71
- Locations
- 3
- Primary Endpoint
- Response duration
Study Overview
Brief Summary
RATIONALE: Drugs used in chemotherapy, such as gemcitabine, paclitaxel, and cisplatin, 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 II trial is studying how well giving gemcitabine together with paclitaxel and cisplatin works in treating patients with advanced transitional cell cancer of the urothelium.
Detailed Description
OBJECTIVES:
- Determine response to gemcitabine hydrochloride, paclitaxel, and cisplatin (GTP) among patients with regional or distant metastases of transitional cell carcinoma of the urothelium or local/regional recurrence after cystoprostatectomy.
- Determine response in patients who receive GTP as the initial chemotherapeutic treatment as well as in patients who have received prior chemotherapy.
- Determine response duration, freedom from progression, and overall survival.
- Assess the toxicity of GTP.
OUTLINE: This is an open-label study. Patients are stratified according to prior chemotherapy (yes vs no).
Patients receive paclitaxel IV over 3 hours and cisplatin IV over 1 hour on day 1 and gemcitabine hydrochloride IV over 30 minutes on days 1 and 8. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity.
Patients achieving a partial response or complete response undergo surgical restaging and debulking. Four to 6 weeks later, patients receive 2 additional courses of chemotherapy.
Study Design
- Study Type
- Interventional
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 120 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •DISEASE CHARACTERISTICS:
- •Histologically confirmed transitional cell carcinoma (TCC) of the urothelium (bladder, renal pelvis, or ureter) or TCC with squamous or glandular elements
- •No pure squamous cell carcinoma or adenocarcinoma
- •Disease not amenable to local curative treatment
- •Regional or distant metastases of TCC of the urothelium OR local/regional recurrence after cystectomy, cystoprostatectomy, nephroureterectomy, or ureterectomy
- •If regional metastases present alone, histological confirmation of the metastases is required
- •No clinically evident brain metastases
- •PATIENT CHARACTERISTICS:
- •ECOG performance status 0 or 1
- •Granulocyte count ≥ 1,500/mm^3
- •Platelet count ≥ 100,000/mm^3
- •Hemoglobin ≥ 10 g/dL
- •Creatinine ≤ 1.6 mg/mL
- •Bilirubin ≤ 1.8 mg/mL
- •SGOT ≤ 3 times upper limit of normal
- •Life expectancy > 3 months
- •No known sensitivity to E. coli-derived products
- •No other prior or concurrent malignancy except active/inactive nonmelanoma skin cancer, adequately treated stage I or II cancer currently in complete remission, or observation-only early-stage prostate cancer
- •No other serious medical illness that would limit survival to < 3 months
- •No psychiatric condition that would limit compliance with study requirements
- •No active uncontrolled bacterial, viral, or fungal infection unless corrected or controlled
- •No hemorrhagic disorder
- •Not pregnant or nursing
- •Negative pregnancy test
- •Fertile patients must use effective contraception
- •PRIOR CONCURRENT THERAPY:
- •See Disease Characteristics
- •No prior systemic chemotherapy regimen
- •Prior intravesical therapy allowed
- •Prior definitive radiation to renal pelvis, ureter, or bladder allowed
- •No concurrent chemotherapy with nonstudy drugs
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Response duration
Overall survival
Response
Freedom from progression
Toxicity
Secondary Outcomes
No secondary outcomes reported