The combination of gemcitabine and carboplatin as first-line treatment in patients with advanced urothelial carcinoma - A Phase II study of the Hellenic Cooperative Oncology Group

被引:64
|
作者
Bamias, A
Moulopoulos, LA
Koutras, A
Aravantinos, G
Fountzilas, G
Pectasides, D
Kastritis, E
Gika, D
Skarlos, D
Linardou, H
Kalofonos, HP
Dimopoulos, MA
机构
[1] Univ Athens, Sch Med, Dept Clin Therapeut, Athens 12462, Greece
[2] Univ Athens, Sch Med, Dept Radiol, GR-11527 Athens, Greece
[3] Univ Patras, Sch Med, Dept Med, Oncol Sect, Rion, Greece
[4] Agii Anargiri Canc Hosp, Dept Med Oncol 3, Athens, Greece
[5] Aristotle Univ Thessaloniki, Sch Med, Oncol Sect, GR-54006 Thessaloniki, Greece
[6] Metaxas Mem Hosp, Dept Med Oncol 2, Piraeus, Greece
[7] Henry Dunan Med Ctr, Dept Oncol, Athens, Greece
[8] Metropolitan Hosp, Dept Med Oncol, Athens, Greece
关键词
bladder carcinoma; carboplatin; gemcitabine; activity; first-line treatment;
D O I
10.1002/cncr.21604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The toxicity of platinum-based combinations represents a common. problem for patients with advanced urothelial carcinoma. The authors previously reported encouraging efficacy for the combination of carboplatin and gemcitabine in patients considered to be unfit for cisplatin-based treatment. The objective of the current multicenter Phase II Study was to evaluate the safety and efficacy of the combination of gemcitabine and carboplatin as first-line treatment in unselected patients with advanced urothelial carcinoma. METHODS. Patients with previously untreated, bidimensionally measurable, inoperable or metastatic urothelial carcinoma were treated with carboplatin, area tinder the concentration Curve of 5 (Day 1) and gemcitabine at a dose of 1000 mg/m(2) (Days 1 and 8), every 21 days for a total of 6 cycles. RESULTS. Sixty patients (49 men and 11 women, with a median age of 69 yrs) were enrolled in the Current study. Intent-to-treat analysis demonstrated an objective response rate (ORR) of 38.4% (95% confidence interval [95% CI], 26-51.8%) (11.7% complete responses and 26.7% partial responses). The median time to disease progression was 7.6 months (95% Cl, 4.5-10.7 mos) and the median overall survival was 16.3 months (95% Cl, 12-20.6 mos). The median survival was comparable to that reported for the combination of methotrexate, vinblastine, doxorubicin, and cisplatin (M-VAC) according to the Memorial Sloan-Kettering Cancer Center prognostic model for patients with similar baseline prognostic features. Grade 3 or 4 toxicity (according to the National Cancer Institute Common Toxicity Criteria [version 2.0]) included anemia (18%), thrombocytopenia (23%), and neutropenia (52%), with 7 episodes of febrile neutropenia (11%) reported. Non-hematologic toxicity was rare. One toxic death occurred during the study. CONCLUSIONS. The combination of gemcitabine and carboplatin appears to have considerable activity as the first-line treatment Of Unselected patients with advanced urothelial carcinoma with manageable toxicity, and deserves further evaluation in this setting.
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收藏
页码:297 / 303
页数:7
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