Department of Urology, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku, Sagamihara 252-0374, Japan.
Int J Mol Sci. 2022 Oct 11;23(20):12119. doi: 10.3390/ijms232012119.
An investigation of alternatives to immune checkpoint inhibitors for advanced urothelial cancer (aUC), with biologic information, is urgently needed. Clinical data for 53 patients who received gemcitabine-paclitaxel therapy (GP) as 2nd-line chemotherapy for aUC refractory to platinum-based chemotherapy were retrospectively reviewed. The efficacy and tolerability of GP were evaluated, and the predictive value of phosphoglycerate kinase 1 (PGK1) immunostained in surgical specimens was investigated for treatment outcomes in 1st- and 2nd-line chemotherapy. GP was associated with an objective response rate of 35.8% and a median overall survival duration of 12.3 months. Multivariate analysis showed that PS2 and 1st- and 2nd-line non-response are independent predictors of worse progression-free survival and that PS2 and 1st-line non-response are independent predictors of worse overall survival. Adverse events were manageable, and no therapy-related deaths occurred. Non-response rates to 1st-line chemotherapy were significantly higher in patients with a high expression of PGK1 in the nucleus than in those with low expression ( = 0.006). Our study demonstrates the efficacy and tolerability of 2nd-line GP for patients with aUC who are refractory to platinum-based chemotherapy. Moreover, PGK1 in the nucleus was predictive values for resistance to platinum-based chemotherapy in aUC.
迫切需要对免疫检查点抑制剂治疗晚期尿路上皮癌(aUC)的替代方案进行研究,同时需要提供生物学信息。回顾性分析了 53 例接受吉西他滨-紫杉醇(GP)治疗的患者的临床资料,这些患者对铂类化疗耐药的 aUC 患者接受二线化疗。评估了 GP 的疗效和耐受性,并研究了磷酸甘油酸激酶 1(PGK1)在手术标本中的免疫染色对一线和二线化疗治疗结果的预测价值。GP 的客观缓解率为 35.8%,中位总生存期为 12.3 个月。多变量分析显示 PS2 和一线及二线无反应是无进展生存期更差的独立预测因子,PS2 和一线无反应是总生存期更差的独立预测因子。不良反应可管理,无治疗相关死亡。核内高表达 PGK1 的患者对一线化疗的无反应率明显高于低表达的患者(=0.006)。本研究表明,对于铂类化疗耐药的 aUC 患者,二线 GP 治疗具有疗效和耐受性。此外,核内 PGK1 对 aUC 对铂类化疗的耐药性具有预测价值。