Department of Urology, Nara Medical University, Kashihara, Nara, Japan.
Department of Urology, Nara Medical University, Kashihara, Nara, Japan.
Clin Genitourin Cancer. 2022 Apr;20(2):196.e1-196.e9. doi: 10.1016/j.clgc.2021.11.006. Epub 2021 Nov 15.
Response to pembrolizumab after first-line chemotherapy is vital to prolonged survival in advanced, unresectable, and/or metastatic urothelial carcinoma (aUC). However, there are sparse clinical data on host-tumor immune modification by first-line platinum-based chemotherapy. This study investigated the association between response to first-line gemcitabine plus cisplatin (GC) or carboplatin (GCarbo) chemotherapy and response to subsequent pembrolizumab treatment.
A multicenter-derived database registered 454 patients diagnosed with aUC between 2008 and 2020. Of these, 108 patients who received first-line GC or GCarbo followed by second-line or later pembrolizumab were eligible for investigation and were classified into 3 groups: 48 receiving full-dose GC, 21 receiving dose-reduced GC, and 39 receiving GCarbo. Overall survival (OS) was calculated using the Kaplan-Meier method and compared using the log-rank test. Possible factors associated with the response to pembrolizumab were evaluated using binary logistic regression methods.
The rate of patients undergoing surgical removal of the primary organ was higher and creatinine clearance was lower in the dose-reduced GC and GCarbo groups than in the full-dose GC groups. Pembrolizumab responders had significantly better survival benefits than nonresponders. The rate of pembrolizumab responders was much higher in first-line chemotherapy responders than in first-line chemotherapy nonresponders. In contrast to the full-dose GC and GCarbo groups, the pembrolizumab responder rate was lower, and no association was observed between response to first-line chemotherapy and response to pembrolizumab in the dose-reduced GC group.
Cisplatin and carboplatin may play an important role in the antitumor immune response, which could impact the outcome of subsequent pembrolizumab treatment. Given that the rate of response to pembrolizumab after dose-reduced GC chemotherapy was relatively low, this regimen is not recommended for cis-unfit patients with aUC. Further studies are required to understand the mechanisms responsible for the cross-reactivity of platinum and immune checkpoint inhibitors.
在晚期不可切除和/或转移性尿路上皮癌(aUC)中,一线化疗后对 pembrolizumab 的反应对延长生存至关重要。然而,关于一线铂类化疗对宿主-肿瘤免疫修饰的临床数据很少。本研究调查了一线吉西他滨加顺铂(GC)或卡铂(GCarbo)化疗后对反应与随后 pembrolizumab 治疗反应之间的关系。
一个多中心数据库登记了 2008 年至 2020 年间诊断为 aUC 的 454 例患者。其中,108 例患者接受一线 GC 或 GCarbo 化疗后接受二线或二线以上 pembrolizumab 治疗,符合调查条件,分为 3 组:48 例接受全剂量 GC,21 例接受剂量减少的 GC,39 例接受 GCarbo。使用 Kaplan-Meier 法计算总生存期(OS),并使用对数秩检验进行比较。使用二元逻辑回归方法评估与 pembrolizumab 反应相关的可能因素。
剂量减少的 GC 和 GCarbo 组中接受手术切除原发病灶的患者比例较高,且肌酐清除率较低。与非应答者相比,pembrolizumab 应答者的生存获益显著更好。一线化疗应答者的 pembrolizumab 应答率明显高于一线化疗无应答者。与全剂量 GC 和 GCarbo 组相比,剂量减少的 GC 组的 pembrolizumab 应答率较低,且与一线化疗应答与 pembrolizumab 应答之间无关联。
顺铂和卡铂可能在抗肿瘤免疫反应中发挥重要作用,从而影响后续 pembrolizumab 治疗的结果。鉴于剂量减少的 GC 化疗后 pembrolizumab 应答率相对较低,因此不建议将该方案用于 cis 不适合的 aUC 患者。需要进一步研究以了解铂类和免疫检查点抑制剂交叉反应的机制。