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Japanese Journal of Clinical Oncology 30:547-552 (2000)
© 2000 Foundation for Promotion of Cancer Research

Single Agent Paclitaxel as a First-line Therapy in Advanced Urothelial Carcinoma: Its Efficacy and Safety in Patients Even With Pretreatment Renal Insufficiency

Muh-Hwa Yang1,2, Chueh-Chuan Yen1,2, Yen-Hwa Chang2,4, Ruey-Kuen Hsieh3, Jin-Hwang Liu1,2, Tzeon-Jye Chiou1,2, Frank S. Fan1,2, Alex Ton-Ling Lin2,4, William Ji-Shien Huang2,4, Wei-Shu Wang1,2, Kuang-Kuo Chen2,4 and Po-Min Chen1,2,+

1Division of Medical Oncology, Department of Medicine and 4Division of Urology, Department of Surgery, Taipei Veterans General Hospital, 2National Yang-Ming University, School of Medicine and 3Division of Hematology/Oncology, Department of Medicine, Mackay Memorial Hospital – Taipei, Taipei, Taiwan

Background: Cisplatin-based chemotherapy is the mainstay of the treatment for advanced urothelial cancer, but patients with renal insufficiency before therapy are usually contraindicated to receiving platinum-based chemotherapy. Paclitaxel is one of the most promising agents against advanced urothelial carcinoma in recent trials and it can be easily tolerated even in patients with compromised renal function. We conducted a study in order to evaluate the efficacy and safety of paclitaxel as a first-line therapy in advanced urothelial carcinoma patients.

Methods: Thirteen advanced chemo-naive urothelial carcinoma patients with a median age of 71 years were studied, seven of them demonstrating renal insufficiency (pretreatment serum creatinine >=1.5 mg/dl). All 13 patients received a minimum of two cycles of paclitaxel 175 mg/m2, delivered by intravenous infusion for 3 h every 3 weeks.

Results: Four of the 13 patients responded to treatment, a response rate of 30.8%, with two of these achieving complete remission and two showing partial responses. The median overall survival period of all 13 patients was nine months (95% CI: 6.51–11.49) and our study revealed a statistical tendency in the difference of median overall survival time between responders and non-responders (13 months versus 7.5 months, log-rank p = 0.038), although the number of cases was limited. The differences in response rate and median overall survival time, comparing patients with renal insufficiency and those with normal renal function, were not significant. Treatment-related toxicity was mild, with only two (15.4%) patients suffering from grade 3–4 leukopenia. No treatment-related mortality was noted.

Conclusions: Single-agent paclitaxel can be used as a first-line therapy in advanced urothelial carcinoma patients, and is especially suitable for those with pretreatment renal insufficiency, since the antitumor activity is significant while toxicity is well tolerated.

+ For reprints and all correspondence: Po-Min Chen, Division of Medical Oncology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Taipei 112, Taiwan. E-mail: pmchen@vghtpe.gov.tw


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