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Feasiblity study of gemcitabine and cisplatin administered every two weeks in patients with advanced urothelial tumors and impaired renal function
Carles, J; Suárez, C; Mesía, C; Nogué, M; Font, A; Doménech, M; Suárez, M; Tusquets, I; Gallén, M; Albanell, J; Fabregat, X.
Afiliación
  • Carles, J; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Suárez, C; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Mesía, C; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Nogué, M; Hospital General de Vic. Barcelona. Spain
  • Font, A; Hospital Universitari Germans Trias i Pujol. Barcelona. Spain
  • Doménech, M; Centre Althaia. Barcelona. Spain
  • Suárez, M; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Tusquets, I; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Gallén, M; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Albanell, J; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
  • Fabregat, X; Universitat Autónoma de Barcelona. Hospital del Mar. Spain
Clin. transl. oncol. (Print) ; 8(10): 755-757, oct. 2006. tab
Article en En | IBECS | ID: ibc-125324
Biblioteca responsable: ES1.1
Ubicación: BNCS
ABSTRACT

OBJECTIVES:

Cisplatin-based combination chemotherapy is the mainstay of treatment for advanced bladder cancer. However, full doses of cisplatin cannot be delivered in patients with impaired renal function. Our aim was to prove the feasibility of a gemcitabine and low-dose cisplatin regimen, delivered every two weeks in patients with impaired renal function. MATERIAL AND

METHODS:

Patients with locally advanced or metastatic bladder cancer with creatinine clearance between 35-60 ml/min received gemcitabine 2500 mg/m2 and cisplatin 35 mg/m2 on day 1, every 14 days.

RESULTS:

Between January 2004 and March 2005, 17 patients were treated. Mean creatinine clearance was 47.8 ml/min (range 37-59 ml/min). Four patients had previously received chemotherapy with gemcitabine and/ or platinum. Median number of cycles per patient was 5 (1-13). No patient developed renal toxicity or worsening of renal function. Main toxicities were (grade 3/4) Anemia 2/1; leucopenia 1/2; trombopenia 1/1. There was one toxic death related to metabolic acidosis, secondary to vomiting. Among 16 patients evaluable for response, we observed one complete response, 7 partial responses (ORR 53.3%; IC 95% 28.1-78.5%), 6 stabilizations (37.5%) and 2 progressions (12.5%).

CONCLUSIONS:

Gemcitabine and low-dose cisplatin is a safe and feasible combination in patients with poor renal function. Response rates seem similar to those previously described with standard schedules of this combination (AU)
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Colección: 06-national / ES Base de datos: IBECS Asunto principal: Carcinoma de Células Transicionales / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Antimetabolitos Antineoplásicos / Antineoplásicos Límite: Aged / Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2006 Tipo del documento: Article
Buscar en Google
Colección: 06-national / ES Base de datos: IBECS Asunto principal: Carcinoma de Células Transicionales / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Antimetabolitos Antineoplásicos / Antineoplásicos Límite: Aged / Female / Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2006 Tipo del documento: Article