Ann Oncol. 2011 Feb;22(2):288-94. doi: 10.1093/annonc/mdq398. Epub 2010 Aug 2.
The second-line chemotherapeutic treatment for metastatic urothelial cancer (UC) after failure of cisplatin-based first-line therapy needs to be improved. Based on encouraging phase II data of gemcitabine and paclitaxel (Taxol) (GP), this trial was designed to compare a short-term (arm A) versus a prolonged (arm B) second-line combination chemotherapy of GP.
Of 102 randomized patients, 96 were eligible for analysis. Primary end point was overall survival (OS). Secondary end points were progression-free survival (PFS), objective response rates (ORR) and toxicity.
Neither OS [arm A: 7.8 (95% CI: 4.2-11.4), arm B: 8.0 (95% CI: 4.9-11.1) months] and PFS [arm A: 4.0 (95% CI: 0-8.0), arm B: 3.1 (95% CI: 1.9-4.2) months] nor ORR (arm A: 37.5%, arm B: 41.5%) were significantly different. On prolonged treatment, more patients experienced severe anemia (arm A: 6.7% versus arm B: 26.7% grade III/IV anemia; P = 0.011). In six patients, treatment was stopped during the first cycle due to disease progression or toxicity. Two patients died due to treatment-related toxic effects.
Due to rapid tumor progression and toxicity at this dosage and schedule in a multicenter setting, it was not feasible to deliver a prolonged regimen. However, a high response rate of ∼40% makes GP a promising second-line treatment option for patients with metastatic UC.
顺铂为基础的一线治疗失败后,转移性尿路上皮癌(UC)的二线化疗治疗需要改进。基于吉西他滨联合紫杉醇(Taxol)(GP)的Ⅱ期临床试验结果令人鼓舞,本试验旨在比较 GP 短期(A 组)与长期(B 组)二线联合化疗。
102 例随机患者中,96 例符合分析条件。主要终点为总生存期(OS)。次要终点为无进展生存期(PFS)、客观缓解率(ORR)和毒性。
OS[A 组:7.8(95%CI:4.2-11.4),B 组:8.0(95%CI:4.9-11.1)个月]、PFS[A 组:4.0(95%CI:0-8.0),B 组:3.1(95%CI:1.9-4.2)个月]和 ORR(A 组:37.5%,B 组:41.5%)均无显著差异。在长期治疗中,更多患者发生严重贫血(A 组:6.7%,B 组:26.7%级/IV 贫血;P=0.011)。在 6 例患者中,由于疾病进展或毒性,在第一个周期中停止治疗。两名患者因治疗相关毒性反应死亡。
由于在多中心环境中该剂量和方案下肿瘤进展迅速且毒性较大,无法进行长期治疗。然而,约 40%的高缓解率使 GP 成为转移性 UC 患者有前途的二线治疗选择。