Tanya Jindal, Cindy Jiang, Omar Alhalabi, Amanda Nizam, Charles Nguyen, Rafee Talukder, Dimitra Bakaloudi, Matthew Davidsohn, Dory Freeman, Michael Glover, Ali Raza Khaki, Sean Evans, Emily Lemke, Rohit Bose, Woogwang Sim, Cameron Pywell, Arnab Basu, Deepak Kilari, Pedro C Barata, Mehmet A Bilen, Yousef Zakharia, Matthew I Milowsky, Sumit A Shah, Joaquim Bellmunt, Petros Grivas, Hamid Emamekhoo, Nancy B Davis, Shilpa Gupta, Christopher Hoimes, Matthew T Campbell, Ajjai Alva, Vadim S Koshkin
{"title":"Genomic Biomarkers Associated with Enfortumab Vedotin Outcomes for Patients with Advanced Urothelial Carcinoma: Analysis of UNITE Study Data.","authors":"Tanya Jindal, Cindy Jiang, Omar Alhalabi, Amanda Nizam, Charles Nguyen, Rafee Talukder, Dimitra Bakaloudi, Matthew Davidsohn, Dory Freeman, Michael Glover, Ali Raza Khaki, Sean Evans, Emily Lemke, Rohit Bose, Woogwang Sim, Cameron Pywell, Arnab Basu, Deepak Kilari, Pedro C Barata, Mehmet A Bilen, Yousef Zakharia, Matthew I Milowsky, Sumit A Shah, Joaquim Bellmunt, Petros Grivas, Hamid Emamekhoo, Nancy B Davis, Shilpa Gupta, Christopher Hoimes, Matthew T Campbell, Ajjai Alva, Vadim S Koshkin","doi":"10.1016/j.euo.2024.12.006","DOIUrl":null,"url":null,"abstract":"<p><p>Enfortumab vedotin (EV) is used as monotherapy or combined with pembrolizumab in advanced urothelial carcinoma (aUC), but biomarker data associated with EV outcomes are limited. We identified 170 patients in the UNITE study who received EV monotherapy and had molecular biomarker data available. Outcomes for groups with and without a particular biomarker were compared using logistic regression (unadjusted) for the objective response rate (ORR), and a log-rank test and Cox proportional-hazard models (CPHMs) for progression-free survival (PFS) and overall survival (OS) from EV initiation. Molecular biomarkers were also evaluated in separate multivariable analyses using CPHMs that accounted for clinical characteristics. Median patient age was 70 yr; 78% of the cohort were male and 65% had pure UC histology. Median PFS was shorter for patients with CDKN2A alterations (4.6 vs 6 mo; p = 0.024) and for patients with CDKN2B alterations (4.4 vs 6 mo; p = 0.008). Median OS was longer for patients with high tumor mutational burden (13.6 vs 8.3 mo; p = 0.014). ORR was higher for patients with TSC1 alterations (87% vs 51%; p = 0.018). In multivariable analyses, CDKN2A and CDKN2B alterations were associated with inferior median PFS. This multi-institutional retrospective study of patients with aUC identified potential biomarkers associated with EV monotherapy outcomes that should be further investigated. PATIENT SUMMARY: We investigated genetic changes in urinary tract tumors that might be associated with response to enfortumab vedotin (EV) treatment in patients with advanced disease. Survival after EV treatment was longer for tumors with a higher number of mutations than for tumors with fewer mutations. However, mutations in two genes (CDKN2A and CDKN2B) were associated with worse outcomes after EV treatment. These findings will not affect current clinical practice, but should be investigated further in future studies.</p>","PeriodicalId":12256,"journal":{"name":"European urology oncology","volume":" ","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European urology oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.euo.2024.12.006","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Enfortumab vedotin (EV) is used as monotherapy or combined with pembrolizumab in advanced urothelial carcinoma (aUC), but biomarker data associated with EV outcomes are limited. We identified 170 patients in the UNITE study who received EV monotherapy and had molecular biomarker data available. Outcomes for groups with and without a particular biomarker were compared using logistic regression (unadjusted) for the objective response rate (ORR), and a log-rank test and Cox proportional-hazard models (CPHMs) for progression-free survival (PFS) and overall survival (OS) from EV initiation. Molecular biomarkers were also evaluated in separate multivariable analyses using CPHMs that accounted for clinical characteristics. Median patient age was 70 yr; 78% of the cohort were male and 65% had pure UC histology. Median PFS was shorter for patients with CDKN2A alterations (4.6 vs 6 mo; p = 0.024) and for patients with CDKN2B alterations (4.4 vs 6 mo; p = 0.008). Median OS was longer for patients with high tumor mutational burden (13.6 vs 8.3 mo; p = 0.014). ORR was higher for patients with TSC1 alterations (87% vs 51%; p = 0.018). In multivariable analyses, CDKN2A and CDKN2B alterations were associated with inferior median PFS. This multi-institutional retrospective study of patients with aUC identified potential biomarkers associated with EV monotherapy outcomes that should be further investigated. PATIENT SUMMARY: We investigated genetic changes in urinary tract tumors that might be associated with response to enfortumab vedotin (EV) treatment in patients with advanced disease. Survival after EV treatment was longer for tumors with a higher number of mutations than for tumors with fewer mutations. However, mutations in two genes (CDKN2A and CDKN2B) were associated with worse outcomes after EV treatment. These findings will not affect current clinical practice, but should be investigated further in future studies.
Enfortumab vedotin (EV)用于晚期尿路上皮癌(aUC)的单药治疗或与派姆单抗联合治疗,但与EV结果相关的生物标志物数据有限。我们在UNITE研究中确定了170例接受EV单药治疗并有分子生物标志物数据的患者。使用逻辑回归(未调整)的客观缓解率(ORR), log-rank检验和Cox比例风险模型(CPHMs)的无进展生存期(PFS)和总生存期(OS)对有和没有特定生物标志物组的结果进行比较。分子生物标志物也在单独的多变量分析中进行评估,使用cphm来解释临床特征。患者年龄中位数为70岁;78%为男性,65%为纯UC组织学。CDKN2A基因改变患者的中位PFS较短(4.6 vs 6个月;p = 0.024)和CDKN2B改变患者(4.4 vs 6个月;p = 0.008)。肿瘤突变负担高的患者中位生存期更长(13.6 vs 8.3个月;p = 0.014)。TSC1改变患者的ORR更高(87% vs 51%;p = 0.018)。在多变量分析中,CDKN2A和CDKN2B的改变与较低的中位PFS相关。这项针对aUC患者的多机构回顾性研究确定了与EV单药治疗结果相关的潜在生物标志物,这些生物标志物应进一步研究。患者总结:我们研究了可能与晚期疾病患者对强制维多汀(EV)治疗反应相关的尿路肿瘤基因变化。突变数量较多的肿瘤比突变较少的肿瘤在EV治疗后存活时间更长。然而,两个基因(CDKN2A和CDKN2B)的突变与EV治疗后较差的结果相关。这些发现不会影响目前的临床实践,但应在未来的研究中进一步调查。
期刊介绍:
Journal Name: European Urology Oncology
Affiliation: Official Journal of the European Association of Urology
Focus:
First official publication of the EAU fully devoted to the study of genitourinary malignancies
Aims to deliver high-quality research
Content:
Includes original articles, opinion piece editorials, and invited reviews
Covers clinical, basic, and translational research
Publication Frequency: Six times a year in electronic format