Bamias Aristotle, Moulopoulos Lia A, Koutras Aggelos, Aravantinos Gerassimos, Fountzilas George, Pectasides Dimitris, Kastritis Efstathios, Gika Dimitros, Skarlos Dimosthenis, Linardou Helena, Kalofonos Haralambos P, Dimopoulos Meletios A
Department of Clinical Therapeutics, Athens University, School of Medicine, Athens, Greece.
Cancer. 2006 Jan 15;106(2):297-303. doi: 10.1002/cncr.21604.
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.
Patients with previously untreated, bidimensionally measurable, inoperable or metastatic urothelial carcinoma were treated with carboplatin, area under 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.
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% CI, 4.5-10.7 mos) and the median overall survival was 16.3 months (95% CI, 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. Nonhematologic toxicity was rare. One toxic death occurred during the study.
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.
铂类联合化疗的毒性是晚期尿路上皮癌患者面临的常见问题。作者之前报道了卡铂和吉西他滨联合方案对那些被认为不适合顺铂治疗的患者具有令人鼓舞的疗效。当前这项多中心II期研究的目的是评估吉西他滨和卡铂联合方案作为晚期尿路上皮癌未选择患者一线治疗的安全性和疗效。
既往未治疗、二维可测量、无法手术或转移性尿路上皮癌患者接受卡铂治疗,浓度曲线下面积为5(第1天),吉西他滨剂量为1000mg/m²(第1天和第8天),每21天为一个周期,共6个周期。
60例患者(49例男性和11例女性,中位年龄69岁)入组本研究。意向性分析显示客观缓解率(ORR)为38.4%(95%置信区间[95%CI],26 - 51.8%)(完全缓解率为11.7%,部分缓解率为26.7%)。疾病进展的中位时间为7.6个月(95%CI,4.5 - 10.7个月),中位总生存期为16.3个月(95%CI,12 - 20.6个月)。根据纪念斯隆凯特琳癌症中心针对具有相似基线预后特征患者的预后模型,该中位生存期与甲氨蝶呤、长春碱、阿霉素和顺铂联合方案(M - VAC)报道的生存期相当。3级或4级毒性(根据美国国立癌症研究所通用毒性标准[第2.0版])包括贫血(18%)、血小板减少(23%)和中性粒细胞减少(52%),报道有发热性中性粒细胞减少7例(11%)。非血液学毒性罕见。研究期间发生1例毒性死亡。
吉西他滨和卡铂联合方案作为晚期尿路上皮癌未选择患者的一线治疗似乎具有相当的活性,且毒性可控,值得在此背景下进一步评估。