Ondřej Fiala, Sebastiano Buti, Kazutoshi Fujita, Alfonso Gómez de Liaño, Wataru Fukuokaya, Takahiro Kimura, Takafumi Yanagisawa, Patrizia Giannatempo, Martin Angel, Alessia Mennitto, Javier Molina-Cerrillo, Maria T Bourlon, Andrey Soares, Hideki Takeshita, Fabio Calabrò, Cinzia Ortega, Jakub Kucharz, Michele Milella, Emmanuel Seront, Se Hoon Park, Deniz Tural, Giovanni Benedetti, Yüksel Ürün, Nicola Battelli, Bohuslav Melichar, Alexandr Poprach, Tomas Buchler, Jindřich Kopecký, Vincenza Conteduca, Fernando Sabino Marques Monteiro, Francesco Massari, Shilpa Gupta, Matteo Santoni
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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<sup>EV</sup> 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.</p>","PeriodicalId":10267,"journal":{"name":"Clinical & Experimental Metastasis","volume":"42 2","pages":"18"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11842414/pdf/","citationCount":"0","resultStr":"{\"title\":\"Concomitant medications in patients with metastatic urothelial carcinoma receiving enfortumab vedotin: real-world data from the ARON-2<sup>EV</sup> study.\",\"authors\":\"Ondřej Fiala, Sebastiano Buti, Kazutoshi Fujita, Alfonso Gómez de Liaño, Wataru Fukuokaya, Takahiro Kimura, Takafumi Yanagisawa, Patrizia Giannatempo, Martin Angel, Alessia Mennitto, Javier Molina-Cerrillo, Maria T Bourlon, Andrey Soares, Hideki Takeshita, Fabio Calabrò, Cinzia Ortega, Jakub Kucharz, Michele Milella, Emmanuel Seront, Se Hoon Park, Deniz Tural, Giovanni Benedetti, Yüksel Ürün, Nicola Battelli, Bohuslav Melichar, Alexandr Poprach, Tomas Buchler, Jindřich Kopecký, Vincenza Conteduca, Fernando Sabino Marques Monteiro, Francesco Massari, Shilpa Gupta, Matteo Santoni\",\"doi\":\"10.1007/s10585-025-10335-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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<sup>EV</sup> 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). 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引用次数: 0
摘要
转移性尿路上皮癌(mUC)的患者通常是老年人,并且经常有其他合并症,需要使用联合药物。在我们的研究中,我们评估了同时使用抗生素(ATBs)、质子泵抑制剂(PPIs)、皮质类固醇、他汀类药物、二甲双胍和胰岛素与患者预后的关系,并验证了同时使用药物评分在接受强制维多汀(EV)单药治疗的mUC患者中的预后作用。纳入ARON-2EV回顾性研究的436例患者的数据根据基线时使用的伴随药物进行分析。最后,根据ATBs、皮质类固醇和PPIs的伴随用药评分将患者分为3个危险组。统计分析采用Fisher精确检验、Kaplan-Meier法、log-rank检验和单因素/多因素Cox比例风险回归模型。与非ATB使用者相比,ATB使用者的生存结果较差(OS: 7.3个月,95%CI 5.0 - 12.3 vs 13.7个月,95%CI 12.2 - 47.3, p = 0.001;PFS: 5.1个月95%CI 3.3 - 17.7 vs 8.3个月,95%CI 7.1 - 47.3, p = 0.001),皮质类固醇使用者与非使用者(OS: 8.4个月,95%CI 6.6 - 10.0 vs 14.2个月,95%CI 12.7 - 47.3, p = 0.001)
Concomitant medications in patients with metastatic urothelial carcinoma receiving enfortumab vedotin: real-world data from the ARON-2EV study.
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-2EV 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.
期刊介绍:
The Journal''s scope encompasses all aspects of metastasis research, whether laboratory-based, experimental or clinical and therapeutic. It covers such areas as molecular biology, pharmacology, tumor biology, and clinical cancer treatment (with all its subdivisions of surgery, chemotherapy and radio-therapy as well as pathology and epidemiology) insofar as these disciplines are concerned with the Journal''s core subject of metastasis formation, prevention and treatment.