Department of Urology, Graduate School of Medicine, Osaka City University, 1-4-3 Asahimachi, Abeno, Osaka, 545-8585, Japan.
Int J Clin Oncol. 2018 Oct;23(5):944-950. doi: 10.1007/s10147-018-1288-1. Epub 2018 May 21.
The aim of this study was to evaluate the efficacy and toxicities of second-line chemotherapy regimens with docetaxel and gemcitabine (GD), or paclitaxel and gemcitabine (GP) for advanced or metastatic urothelial carcinoma (UC) that did not respond to first-line platinum-based chemotherapy.
From 2002 to 2017, 78 patients with metastatic UCs that progressed after platinum-based chemotherapy were treated with either GD (n = 41) or GP (n = 37). We compared these two different regimens by analyzing their efficacy and toxicities in a retrospective manner.
Of the 78 patients enrolled in this study, it was possible to determine treatment efficacy in 70; the proportion of patients with objective response and disease control were 8.6 (9/70) and 54.3% (38/70), respectively. The median progression-free survival and overall survival in the total population (GP and GD) were 3.5 (95% CI 0.6-53.3) and 9.6 months (95% CI 1.2-53.3), respectively. There was no significant difference between the two regimens (GD or GP) regarding survival outcomes. Treatment-related adverse events were mostly manageable, but one patient died as a result of febrile neutropenia. The presence of liver metastasis and anemia (Hb < 10.0 g/dl) was prognostic factors for worse survival.
Combination chemotherapy with either GP or GD was a favorable and well-tolerated second-line treatment regimen for patients with advanced or metastatic UC following the failure of a platinum-based regimen. Further study using a large prospective cohort is needed to identify patients who will benefit from second-line combination therapy.
本研究旨在评估多西他赛联合吉西他滨(GD)或紫杉醇联合吉西他滨(GP)二线化疗方案治疗铂类化疗失败的晚期或转移性尿路上皮癌(UC)的疗效和毒性。
2002 年至 2017 年,78 例铂类化疗后进展的转移性 UC 患者接受 GD(n=41)或 GP(n=37)治疗。我们通过回顾性分析比较了这两种不同方案的疗效和毒性。
本研究共纳入 78 例患者,70 例可评估疗效;客观缓解率和疾病控制率分别为 8.6%(9/70)和 54.3%(38/70)。全人群(GP 和 GD)的中位无进展生存期和总生存期分别为 3.5 个月(95%CI 0.6-53.3)和 9.6 个月(95%CI 1.2-53.3)。两种方案(GD 或 GP)的生存结局无显著差异。治疗相关不良事件大多可管理,但有 1 例患者因发热性中性粒细胞减少而死亡。肝转移和贫血(Hb<10.0 g/dl)是影响生存的预后因素。
GP 或 GD 联合化疗是铂类化疗失败的晚期或转移性 UC 患者的一种有利且耐受良好的二线治疗方案。需要进一步使用大型前瞻性队列研究来确定哪些患者将从二线联合治疗中获益。