Fiala Ondřej, Buti Sebastiano, Fujita Kazutoshi, de Liaño Alfonso Gómez, Fukuokaya Wataru, Kimura Takahiro, Yanagisawa Takafumi, Giannatempo Patrizia, Angel Martin, Mennitto Alessia, Molina-Cerrillo Javier, Bourlon Maria T, Soares Andrey, Takeshita Hideki, Calabrò Fabio, Ortega Cinzia, Kucharz Jakub, Milella Michele, Seront Emmanuel, Park Se Hoon, Tural Deniz, Benedetti Giovanni, Ürün Yüksel, Battelli Nicola, Melichar Bohuslav, Poprach Alexandr, Buchler Tomas, Kopecký Jindřich, Conteduca Vincenza, Monteiro Fernando Sabino Marques, Massari Francesco, Gupta Shilpa, Santoni Matteo
Department of Oncology and Radiotherapeutics, Faculty of Medicine and University Hospital in Pilsen, Charles University Prague, Alej Svobody 80, 304 60, Pilsen, Czech Republic.
Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Clin Exp Metastasis. 2025 Feb 20;42(2):18. doi: 10.1007/s10585-025-10335-4.
Patients with metastatic urothelial carcinoma (mUC) are typically elderly and often have other comorbidities that require the use of concomitant medications. In our study we evaluated the association of concomitant use of antibiotics (ATBs), proton pump inhibitors (PPIs), corticosteroids, statins, metformin and insulin with patient outcomes and we validated the prognostic role of a concomitant drug score in mUC patients treated with enfortumab vedotin (EV) monotherapy. Data from 436 patients enrolled in the ARON-2 retrospective study were analyzed according to the concomitant medications used at baseline. Finally, the patients were stratified into three risk groups according to the concomitant drug score based on ATBs, corticosteroids and PPIs. Statistical analysis involved Fisher exact test, Kaplan-Meier method, log-rank test, and univariate/multivariate Cox proportional hazard regression models. Inferior survival outcomes were observed in ATB users compared to non-users (OS: 7.3 months, 95%CI 5.0 - 12.3 vs 13.7 months, 95%CI 12.2 - 47.3, p = 0.001; PFS: 5.1 months 95%CI 3.3 - 17.7 vs 8.3 months, 95%CI 7.1 - 47.3, p = 0.001) and also in corticosteroid users compared to non-users (OS: 8.4 months, 95%CI 6.6 - 10.0 vs 14.2 months, 95%CI 12.7 - 47.3, p < 0.001; PFS: 6.0 months 95%CI 4.6 - 7.9 vs 8.9 months, 95%CI 7.2 - 47.3, p = 0.004). In the Cox multivariate analysis, the concomitant drug score was a significant factor predicting both OS (HR = 1.32 [95% CI 1.03 - 1.68], p = 0.026) and PFS (HR = 1.23 [95% CI 1.01 - 1.51], p = 0.044). Our findings suggest detrimental impact of concomitant use of ATBs and corticosteroids on survival outcomes and the prognostic utility of the concomitant drug score in previously treated mUC patients receiving EV.
转移性尿路上皮癌(mUC)患者通常为老年人,且常伴有其他需要使用伴随药物的合并症。在我们的研究中,我们评估了抗生素(ATB)、质子泵抑制剂(PPI)、皮质类固醇、他汀类药物、二甲双胍和胰岛素的联合使用与患者预后的关联,并验证了联合用药评分在接受恩杂鲁胺(EV)单药治疗的mUC患者中的预后作用。根据基线时使用的伴随药物,对ARON - 2回顾性研究中纳入的436例患者的数据进行了分析。最后,根据基于ATB、皮质类固醇和PPI的联合用药评分,将患者分为三个风险组。统计分析包括Fisher精确检验、Kaplan - Meier法、对数秩检验以及单变量/多变量Cox比例风险回归模型。与未使用者相比,ATB使用者的生存结果较差(总生存期:7.3个月,95%置信区间5.0 - 12.3 vs 13.7个月,95%置信区间12.2 - 47.3,p = 0.001;无进展生存期:5.1个月,95%置信区间3.3 - 17.7 vs 8.3个月,95%置信区间7.1 - 47.3,p = 0.001),皮质类固醇使用者与未使用者相比也是如此(总生存期:8.4个月,95%置信区间6.6 - 10.0 vs 14.2个月,95%置信区间12.7 - 47.3,p < 0.001;无进展生存期:6.0个月,95%置信区间4.6 - 7.9 vs 8.9个月,95%置信区间7.2 - 47.3,p = 0.004)。在Cox多变量分析中,联合用药评分是预测总生存期(风险比 = 1.32 [95%置信区间1.03 - 1.68],p = 0.026)和无进展生存期(风险比 = 1.23 [95%置信区间1.01 - 1.51],p = 0.044)的重要因素。我们的研究结果表明,ATB和皮质类固醇的联合使用对生存结果有不利影响,且联合用药评分在接受EV治疗的既往mUC患者中具有预后价值。