Necchi Andrea, Pond Gregory R, Raggi Daniele, Giannatempo Patrizia, Vogelzang Nicholas J, Grivas Petros, Galsky Matthew D, Bellmunt Joaquim, Sonpavde Guru
Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
McMaster University, Hamilton, Ontario, Canada.
Clin Genitourin Cancer. 2017 Feb;15(1):23-30.e2. doi: 10.1016/j.clgc.2016.05.003. Epub 2016 May 27.
Although gemcitabine plus carboplatin (GCa) is the conventional first-line chemotherapy for cisplatin-ineligible metastatic urothelial carcinoma, its results are suboptimal. A meta-analysis evaluated the results of gemcitabine with either carboplatin or a taxane (GT). Literature was searched for studies including GT (paclitaxel or docetaxel) and GCa. We pooled trial level data including response-rate, progression-free survival, overall survival (OS), and Grade 3 to 4 side effects. Trial characteristics and outcomes were univariably compared between GT and GCa. Those factors, which were recorded in > 12 trials, were analyzed. Multivariable regression models were used adjusting for Eastern Cooperative Oncology Group performance status 2 and the presence of visceral metastases. Each trial was weighted by its sample size. Twenty-seven arms of trials totaling 1032 patients were selected, of which 13 contained GT (n = 484) and 14 GCa (n = 548). The percentage of patients with Eastern Cooperative Oncology Group performance status 2 was statistically significantly different between the 2 groups (median, 8.7% vs. 23.9%; P = .003). No efficacy outcome was statistically significantly different. Median OS was 13.2 months (range, 10-15.8 months) for GT and 10 months (range, 3.3-20 months) for GCa (P = .12). However, statistically significant increases in the frequency of Grade 3 to 4 anemia (P = .010) and thrombocytopenia (P = .010) for GCa, and neuropathy (P = .040) for GT were observed. No difference in OS according to treatment was found multivariably (P = .79). In this analysis, a similar response rate and survival and worse neurotoxicity were observed with GT compared with GCa, for which hematologic toxicity was more frequent. GT is an alternative to GCa for advanced cisplatin-ineligible urothelial cancer.
尽管吉西他滨联合卡铂(GCa)是无法使用顺铂的转移性尿路上皮癌的传统一线化疗方案,但其效果并不理想。一项荟萃分析评估了吉西他滨联合卡铂或紫杉烷(GT)的治疗结果。检索了包括GT(紫杉醇或多西他赛)和GCa的研究文献。我们汇总了试验水平的数据,包括缓解率、无进展生存期、总生存期(OS)以及3至4级副作用。对GT和GCa之间的试验特征和结果进行单变量比较。分析了在超过12项试验中记录的那些因素。使用多变量回归模型对东部肿瘤协作组(Eastern Cooperative Oncology Group)体能状态2和内脏转移的存在情况进行校正。每项试验按其样本量加权。共选择了27个试验组,总计1032例患者,其中13个包含GT(n = 484),14个包含GCa(n = 548)。两组患者中东部肿瘤协作组体能状态2的比例在统计学上有显著差异(中位数,8.7%对23.9%;P = 0.003)。没有疗效结果在统计学上有显著差异。GT组的中位OS为13.2个月(范围,10 - 15.8个月),GCa组为10个月(范围,3.3 - 20个月)(P = 0.12)。然而,观察到GCa组3至4级贫血(P = 0.010)和血小板减少症(P = 0.010)的发生率有统计学显著增加,GT组神经病变(P = 0.040)的发生率有统计学显著增加。多变量分析未发现治疗对OS有差异(P = 0.79)。在该分析中,与GCa相比,GT的缓解率和生存率相似,但神经毒性更差,而GCa的血液学毒性更频繁。对于无法使用顺铂的晚期尿路上皮癌,GT是GCa的替代方案。