{"title":"Limited survival benefit in patients diagnosed with glioblastoma post-2016: a SEER population based registry analysis.","authors":"Shaurya Dhingra, Matthew Koshy, Mark Korpics","doi":"10.1007/s00432-025-06171-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The EF14 clinical trial reported an improvement in median overall survival (OS) from 16.0 months to 20.9 months in patients with glioblastoma (GBM) who received treatment with tumor treating fields (TTFs). This study evaluates overall survival in a large population-based cohort of patients with GBM before and after FDA approval of TTFs in 2015.</p><p><strong>Methods: </strong>A total of 27,534 patients from the Surveillance, Epidemiology and End Results (SEER) database with GBM who underwent surgery and post-operative radiotherapy were grouped into three diagnosis periods: those diagnosed pre-temozolomide (2000-2004), those diagnosed post-temozolomide (2005-2015), and those diagnosed post-TTFs (2016-2020). Overall survival (OS) was calculated using the Kaplan-Meier method, and multivariate Cox regression models were employed to estimate hazard ratios (HR).</p><p><strong>Results: </strong>GBM diagnosis in the post-TTFs period was associated with a median OS of 15 months (95% CI 14-15 months) compared to a median OS of 14 months (95% CI 14-14 months, p < 0.001) for GBM diagnosis in the post-temozolomide/pre-TTFs period. 24-months OS was 25.6% (95% CI 24.5-26.8%) in the post-TTFs period and 24.7% (95% CI 24.0-25.4%) in the post-temozolomide/pre-TTFs period. In a multivariate model accounting for clinical characteristics, diagnosis in the post-TTFs period as compared to the post-temozolomide/pre-TTFs period was significantly associated with OS (HR: 0.941, 95% CI 0.912-0.972, p < 0.001).</p><p><strong>Conclusion: </strong>This population-based cohort demonstrated minimal change in survival for patients diagnosed with GBM before and after FDA approval of TTFs in 2015.</p>","PeriodicalId":15118,"journal":{"name":"Journal of Cancer Research and Clinical Oncology","volume":"151 6","pages":"179"},"PeriodicalIF":2.7000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130152/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cancer Research and Clinical Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00432-025-06171-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: The EF14 clinical trial reported an improvement in median overall survival (OS) from 16.0 months to 20.9 months in patients with glioblastoma (GBM) who received treatment with tumor treating fields (TTFs). This study evaluates overall survival in a large population-based cohort of patients with GBM before and after FDA approval of TTFs in 2015.
Methods: A total of 27,534 patients from the Surveillance, Epidemiology and End Results (SEER) database with GBM who underwent surgery and post-operative radiotherapy were grouped into three diagnosis periods: those diagnosed pre-temozolomide (2000-2004), those diagnosed post-temozolomide (2005-2015), and those diagnosed post-TTFs (2016-2020). Overall survival (OS) was calculated using the Kaplan-Meier method, and multivariate Cox regression models were employed to estimate hazard ratios (HR).
Results: GBM diagnosis in the post-TTFs period was associated with a median OS of 15 months (95% CI 14-15 months) compared to a median OS of 14 months (95% CI 14-14 months, p < 0.001) for GBM diagnosis in the post-temozolomide/pre-TTFs period. 24-months OS was 25.6% (95% CI 24.5-26.8%) in the post-TTFs period and 24.7% (95% CI 24.0-25.4%) in the post-temozolomide/pre-TTFs period. In a multivariate model accounting for clinical characteristics, diagnosis in the post-TTFs period as compared to the post-temozolomide/pre-TTFs period was significantly associated with OS (HR: 0.941, 95% CI 0.912-0.972, p < 0.001).
Conclusion: This population-based cohort demonstrated minimal change in survival for patients diagnosed with GBM before and after FDA approval of TTFs in 2015.
背景:EF14临床试验报告,接受肿瘤治疗野(ttf)治疗的胶质母细胞瘤(GBM)患者的中位总生存期(OS)从16.0个月提高到20.9个月。该研究评估了2015年FDA批准ttf前后的大型人群GBM患者的总生存率。方法:从监测、流行病学和最终结果(SEER)数据库中,共有27,534例接受手术和术后放疗的GBM患者被分为三个诊断期:替莫唑胺前诊断期(2000-2004年)、替莫唑胺后诊断期(2005-2015年)和ttf后诊断期(2016-2020年)。采用Kaplan-Meier法计算总生存期(OS),采用多变量Cox回归模型估计风险比(HR)。结果:与中位生存期14个月(95% CI 14-14个月)相比,TTFs后GBM诊断与中位生存期15个月(95% CI 14-14个月)相关。结论:该基于人群的队列显示,2015年FDA批准TTFs前后诊断为GBM的患者的生存变化最小。
期刊介绍:
The "Journal of Cancer Research and Clinical Oncology" publishes significant and up-to-date articles within the fields of experimental and clinical oncology. The journal, which is chiefly devoted to Original papers, also includes Reviews as well as Editorials and Guest editorials on current, controversial topics. The section Letters to the editors provides a forum for a rapid exchange of comments and information concerning previously published papers and topics of current interest. Meeting reports provide current information on the latest results presented at important congresses.
The following fields are covered: carcinogenesis - etiology, mechanisms; molecular biology; recent developments in tumor therapy; general diagnosis; laboratory diagnosis; diagnostic and experimental pathology; oncologic surgery; and epidemiology.