Yang M H, Yen C C, Chang Y H, Hsieh R K, Liu J H, Chiou T J, Fan F S, Lin A T, Huang W J, Wang W S, Chen K K, Chen P M
Division of Medical Oncology, Department of Medicine, Taipei Veterans General Hospital, Taiwan.
Jpn J Clin Oncol. 2000 Dec;30(12):547-52. doi: 10.1093/jjco/hyd142.
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.
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 > or = 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.
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% Cl: 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.
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.
基于顺铂的化疗是晚期尿路上皮癌治疗的主要手段,但治疗前存在肾功能不全的患者通常禁忌接受铂类化疗。紫杉醇是近期试验中治疗晚期尿路上皮癌最有前景的药物之一,即使在肾功能受损的患者中也能很容易耐受。我们开展了一项研究,以评估紫杉醇作为晚期尿路上皮癌患者一线治疗的疗效和安全性。
对13例初治的晚期尿路上皮癌患者进行研究,患者中位年龄71岁,其中7例存在肾功能不全(治疗前血清肌酐≥1.5mg/dl)。所有13例患者均接受至少两个周期的紫杉醇治疗,剂量为175mg/m²,每3周静脉输注3小时。
13例患者中有4例对治疗有反应,反应率为30.8%,其中2例达到完全缓解,2例为部分缓解。13例患者的中位总生存期为9个月(95%CI:6.51 - 11.49),尽管病例数有限,但我们的研究显示,反应者与无反应者的中位总生存时间存在统计学差异倾向(13个月对7.5个月,对数秩检验p = 0.038)。肾功能不全患者与肾功能正常患者在反应率和中位总生存时间上的差异不显著。治疗相关毒性较轻,仅有2例(15.4%)患者出现3 - 4级白细胞减少。未观察到治疗相关死亡。
单药紫杉醇可作为晚期尿路上皮癌患者的一线治疗药物,尤其适用于治疗前存在肾功能不全的患者,因为其抗肿瘤活性显著且毒性耐受性良好。