Department of Oncology, Assaf Harofeh Medical Center, Zerifin 70300, Israel.
Int Braz J Urol. 2012 Jan-Feb;38(1):49-56. doi: 10.1590/s1677-55382012000100007.
Combination of gemcitabine and carboplatin is the accepted treatment for metastatic urothelial cancer patients unfit for cisplatin-based chemotherapy.
Gemcitabine 1000 mg/m² (days 1, 8) and carboplatin AUC- 4.5 (day 1) were given every 21 days to 23 patients with creatinine clearance < 60 mL/min, cardiac ejection fraction < 45% or active ischemia. Patient characteristics included: median age 73 (56-86) years; primary site: bladder 17 (73%), upper tract 6 (27 %) patients; Bajorin 's prognostic groups: good 6 (26%), intermediate 11 (48%) and poor 6 (26%) patients. Data was retrospectively documented. Patients were followed until they expired.
We obtained objective responses in 8 (34.7%) patients, (95% CI, 16.3-57.2%), including one patient with complete response. The median progressionfree survival was 4 (0.2-16.5+) months and the overall survival 8.6 (0.2-45.3+) months. At time of analysis, 4 patients (17%) remained disease free; 3 of them underwent resection of residual disease. Toxicity included: infection in 9 (39%) patients; among them, one died from pneumonia; bleeding ≥ grade 2 in 3 (13%) patients and fatigue grade 3 in 2 (9%) patients. Hematologic toxicity included grade 4 thrombocytopenia in 2 (9%) patients and grade 4 neutropenia in 3 (13%) patients. Five (22%) patients discontinued therapy due to toxicity.
Combination of gemcitabine and carboplatin demonstrated clinical activity in patients with advanced urothelial cancer unfit for cisplatin. It was associated with considerable toxicity. Resection of residual disease is feasible in this population.
对于不适合顺铂化疗的转移性尿路上皮癌患者,吉西他滨联合卡铂是公认的治疗方法。
肌酐清除率<60mL/min、射血分数<45%或有活动性缺血的 23 名患者,每 21 天给予吉西他滨 1000mg/m²(第 1、8 天)和卡铂 AUC-4.5(第 1 天)。患者特征包括:中位年龄 73 岁(56-86 岁);原发部位:膀胱 17 例(73%),上尿路 6 例(27%);Bajorin 预后分组:良好 6 例(26%),中等 11 例(48%),差 6 例(26%)。数据进行了回顾性记录。患者随访至死亡。
我们在 8 名(34.7%)患者中获得了客观缓解,(95%CI,16.3-57.2%),包括 1 名完全缓解患者。中位无进展生存期为 4 个月(0.2-16.5+),总生存期为 8.6 个月(0.2-45.3+)。在分析时,4 名患者(17%)仍无疾病;其中 3 名患者行残余疾病切除术。毒性包括:9 例(39%)患者感染;其中 1 例死于肺炎;3 例(13%)患者出现≥2 级出血,2 例(9%)患者出现 3 级疲劳。血液学毒性包括 2 例(9%)患者出现 4 级血小板减少症和 3 例(13%)患者出现 4 级中性粒细胞减少症。由于毒性,有 5 名患者(22%)停止了治疗。
吉西他滨联合卡铂在不适合顺铂化疗的晚期尿路上皮癌患者中显示出临床疗效。它与相当大的毒性有关。在这一人群中,行残余疾病切除术是可行的。