A Phase II Study of Weekly Docetaxel as Second-Line Chemotherapy in Patients With Metastatic Urothelial Carcinoma

被引:10
|
作者
Kim, Young Saing [1 ]
Lee, Soon Il [2 ]
Park, Se Hoon [3 ]
Park, Silvia [3 ]
Hwang, In Gyu [4 ]
Lee, Sang-Cheol [5 ]
Sun, Jong-Mu [3 ]
Lee, Jeeyun [3 ]
Lim, Ho Yeong [3 ]
机构
[1] Gachon Univ, Gil Med Ctr, Dept Internal Med, Div Hematol & Oncol, Inchon, South Korea
[2] Dankook Univ, Coll Med, Dankook Univ Hosp, Div Hematol Oncol,Dept Med, Cheonan 330715, South Chungcheo, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol,Dept Med, Seoul, South Korea
[4] Chung Ang Univ, Coll Med, Chung Ang Univ Hosp, Div Hematol Oncol,Dept Internal Med, Seoul 156756, South Korea
[5] Soonchunhyang Univ Hosp Cheonan, Dept Internal Med, Div Hematol Oncol, Cheonan, South Korea
关键词
Bladder cancer; Chemotherapy; Docetaxel; Phase II; Second-line; Urothelial carcinoma; TRANSITIONAL-CELL CARCINOMA; RANDOMIZED-TRIAL; WEEKLY PACLITAXEL; LUNG-CANCER; G-CSF; M-VAC; CISPLATIN; PLUS; MULTICENTER; VINFLUNINE;
D O I
10.1016/j.clgc.2015.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present multicenter phase II study evaluated the efficacy and safety of weekly docetaxel as second-line chemotherapy for metastatic urothelial carcinoma. Weekly docetaxel was well tolerated but demonstrated modest activity, with a response rate of 6%, a median progression-free survival (PFS) of 1.4 months, and a median overall survival (OS) of 8.3 months. The dichotomy between PFS and OS was likely associated with subsequent platinum-based chemotherapy received by 58% of the patients. Background: Docetaxel is commonly used for second-line therapy for metastatic urothelial carcinoma (UC). However, myelosuppression is a substantial concern when the traditional 3-week docetaxel cycle is used. The present multicenter phase II study evaluated the efficacy and safety of weekly docetaxel as second-line chemotherapy for metastatic UC. Patients and Methods: Patients with progression after previous platinum-based chemotherapy for advanced or metastatic disease were treated with docetaxel 30 mg/m(2) on days 1 and 8 every 21 days. The primary endpoint was the response rate. Results: The study enrolled 31 patients. Their median age was 64 years (range, 40-79 years). An Eastern Cooperative Oncology Group performance status of 1, liver metastasis, and a hemoglobin level < 10 g/dL were observed in 100%, 32%, and 23% of patients, respectively. Previous platinum-based chemotherapy had been administered for metastatic disease in 29 patients (94%). Although fatigue (13%) and anorexia (6%) were the most frequently observed grade 3 to 4 toxicities, the safety profiles were generally mild and manageable. Two patients (6%) achieved an objective response, which was maintained for 3.0 to 7.8 months. Eight patients experienced disease stabilization (disease control rate, 32%). The median progression-free survival (PFS) and overall survival (OS) were 1.4 months (95% confidence interval [CI], 1.3-1.6) and 8.3 months (95% CI, 5.9-10.6), respectively. A relatively long OS was associated with further salvage platinum-based chemotherapy (n = 18, 58%) showing an encouraging activity (response rate, 44%; median PFS, 4.0 months). Conclusion: Second-line chemotherapy with weekly docetaxel was well tolerated but demonstrated modest activity in patients with metastatic UC. A platinum-based combination as second-line treatment might be considered for selected patients. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:76 / 81
页数:6
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