{"title":"Impact of Genetic Mutations on Response and Time to Progression After Radioembolization of Breast Cancer Liver Metastases.","authors":"Bajnauth Daana, Deipolyi Amy, Annie Frank, Bryce Yolanda","doi":"10.1016/j.jvir.2026.108819","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the association between genetic mutations and clinical outcomes, including response and time to progression, in patients with breast cancer liver metastasis treated with Y-90 radioembolization.</p><p><strong>Materials and methods: </strong>This is a retrospective, single-institution study. 110 female patients with breast cancer liver metastasis who underwent Y-90 radioembolization were included. Genomic profiling was conducted using MSK-IMPACT. Patient demographics and treatment response were collected from electronic medical records and Picture Archiving and Communication System (PACS). Y-90 response was categorized as complete, partial, none, or progression. Time to progression was analyzed in patients with an initial response. Median survival using Kaplan Meier estimation was correlated to genetic mutations. 17 patients died before progression was assessed, and 6 patients were not yet evaluated post-procedure.</p><p><strong>Results: </strong>Overall median survival was 32.8 months (1.3 - 173.0). Patients with the ERBB2 mutation showed the longest median survival (70.2 months [12.5 - 173.0]), while the RAD21 mutation had the shortest median survival (25.5 months [2.4 - 173.0]). KDM5C and CBFB mutations were associated with the highest response rates (100%, p=0.003 and p=0.014, respectively), while the H3C13 mutation was associated with the lowest response rate (0%, p=0.002). Median time to progression was 32.8 months (1.4 - 173.0) in patients with an initial treatment response. The H3F3B mutation was associated with the longest time to progression (105 months [50.2 - 105.0]), while the RUNX1 mutation was associated with the shortest time to progression (1.4 months [1.4 - 36.5]).</p><p><strong>Conclusion: </strong>Specific genetic mutations are associated with survival, response rate, and time to progression after Y-90 radioembolization. This study underscores the potential use of genetic profiling to individualize treatment plans.</p>","PeriodicalId":49962,"journal":{"name":"Journal of Vascular and Interventional Radiology","volume":" ","pages":"108819"},"PeriodicalIF":2.6000,"publicationDate":"2026-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Vascular and Interventional Radiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jvir.2026.108819","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To evaluate the association between genetic mutations and clinical outcomes, including response and time to progression, in patients with breast cancer liver metastasis treated with Y-90 radioembolization.
Materials and methods: This is a retrospective, single-institution study. 110 female patients with breast cancer liver metastasis who underwent Y-90 radioembolization were included. Genomic profiling was conducted using MSK-IMPACT. Patient demographics and treatment response were collected from electronic medical records and Picture Archiving and Communication System (PACS). Y-90 response was categorized as complete, partial, none, or progression. Time to progression was analyzed in patients with an initial response. Median survival using Kaplan Meier estimation was correlated to genetic mutations. 17 patients died before progression was assessed, and 6 patients were not yet evaluated post-procedure.
Results: Overall median survival was 32.8 months (1.3 - 173.0). Patients with the ERBB2 mutation showed the longest median survival (70.2 months [12.5 - 173.0]), while the RAD21 mutation had the shortest median survival (25.5 months [2.4 - 173.0]). KDM5C and CBFB mutations were associated with the highest response rates (100%, p=0.003 and p=0.014, respectively), while the H3C13 mutation was associated with the lowest response rate (0%, p=0.002). Median time to progression was 32.8 months (1.4 - 173.0) in patients with an initial treatment response. The H3F3B mutation was associated with the longest time to progression (105 months [50.2 - 105.0]), while the RUNX1 mutation was associated with the shortest time to progression (1.4 months [1.4 - 36.5]).
Conclusion: Specific genetic mutations are associated with survival, response rate, and time to progression after Y-90 radioembolization. This study underscores the potential use of genetic profiling to individualize treatment plans.
期刊介绍:
JVIR, published continuously since 1990, is an international, monthly peer-reviewed interventional radiology journal. As the official journal of the Society of Interventional Radiology, JVIR is the peer-reviewed journal of choice for interventional radiologists, radiologists, cardiologists, vascular surgeons, neurosurgeons, and other clinicians who seek current and reliable information on every aspect of vascular and interventional radiology. Each issue of JVIR covers critical and cutting-edge medical minimally invasive, clinical, basic research, radiological, pathological, and socioeconomic issues of importance to the field.