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Phase I-II Study of Paclitaxel, Cisplatin, and Gemcitabine in Advanced Transitional-Cell Carcinoma of the Urothelium

From the Hospital General Universitari Vall d’Hebron; Hospital del Mar, Barcelona; Instituto Valenciano de Oncología, Valencia; Hospital 12 de Octubre; Hospital Clínico San Carlos; Departamento de Estadística, Universidad Autónoma de Madrid, Madrid; Hospital General de Vic, Vic; Hospital Lozano-Blesa, Zaragoza; Hospital Marqués de Valdecilla, Santander; Hospital Germans Trias i Pujol, Badalona; Consorci Parc Taulí, Sabadell; and Hospital Mutua de Terrassa, Terrassa, Spain.

Address reprint requests to Joaquim Bellmunt, MD, Medical Oncology Service, Hospital General Universitari Vall d’Hebron. P. Vall d’Hebron 119–129, 08035 Barcelona, Spain; email: bellmunt{at}hg vhebron.es.

PURPOSE: To determine the maximum-tolerated dose and the antitumor activity of a combination of paclitaxel, cisplatin, and gemcitabine in advanced transitional-cell carcinoma (TCC) of the urothelium.

PATIENTS AND METHODS: Patients with measurable, previously untreated, locally advanced or metastatic TCC and with Eastern Cooperative Oncology Group performance status 2 and creatinine clearance 55 mL/min were eligible. Cisplatin was given on day 1 at a fixed dose of 70 mg/m². Paclitaxel and gemcitabine were given on days 1 and 8 at increasing dose levels. Cycles were repeated every 21 days to a maximum of six cycles.

RESULTS: Sixty-one patients were registered. In phase I, 15 patients were entered at four different dose levels. Dose-limiting toxicity consisted of early onset (after the first cycle) grade 2 asthenia (two of six patients) and grade 3 asthenia (one of six patients) at dose level 4. A paclitaxel dose of 80 mg/m² and gemcitabine 1,000 mg/m² was recommended for phase II, and 46 additional patients were entered at this level for a total of 49 patients. Main nonhematologic toxicity was grade 2 asthenia in 18 patients, with early onset in five patients, and grade 3 in four patients. Grade 3/4 neutropenia and thrombocytopenia occurred in 27 (55%) and 11 (22%) patients, respectively. Overall, febrile neutropenia was seen in 11 patients, and one toxic death occurred because of neutropenic sepsis. The combination was active at all dose levels. In total, 58 of 61 eligible patients were assessable for response; 16 complete responses (27.6%) and 29 partial responses (50%) were observed for an overall response rate of 77.6% (95% confidence interval, 60% to 98%). The median survival time (MST) available for the phase I part of the study is 24.0 months. MST has not been reached for the whole group with the current follow-up.

CONCLUSION: This combination of paclitaxel, cisplatin, and gemcitabine is feasible and highly active in patients with advanced TCC of the urothelium. Further evaluation of this regimen in patients with TCC is warranted.

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