Yuxuan Wang,Corinne E Joshu,Samuel D Curtis,Christopher Douville,Vernon A Burk,Meng Ru,Maria Popoli,Janine Ptak,Lisa Dobbyn,Natalie Silliman,Josef Coresh,Eric Boerwinkle,Anna Prizment,Chetan Bettegowda,Kenneth W Kinzler,Nickolas Papadopoulos,Elizabeth A Platz,Bert Vogelstein
{"title":"Detection of cancers three years prior to diagnosis using plasma cell-free DNA.","authors":"Yuxuan Wang,Corinne E Joshu,Samuel D Curtis,Christopher Douville,Vernon A Burk,Meng Ru,Maria Popoli,Janine Ptak,Lisa Dobbyn,Natalie Silliman,Josef Coresh,Eric Boerwinkle,Anna Prizment,Chetan Bettegowda,Kenneth W Kinzler,Nickolas Papadopoulos,Elizabeth A Platz,Bert Vogelstein","doi":"10.1158/2159-8290.cd-25-0375","DOIUrl":null,"url":null,"abstract":"To explore how early can cancers be detected prior to clinical signs or symptoms, we assessed prospectively collected serial plasma samples from the Atherosclerosis Risk in Communities (ARIC) study, including 26 participants diagnosed with cancer and 26 matched controls. At the index time point, eight of these 52 participants scored positively with a multicancer early detection (MCED) test. All eight participants were diagnosed with cancer within 4 months after blood collection. In six of these 8 participants, we were able to assess an earlier plasma sample collected 3.1 to 3.5 years prior to clinical diagnosis. In four of these six participants, the same mutations detected by the MCED test could be identified, but at 8.6 to 79-fold lower mutant allele fractions. These results demonstrate that it is possible to detect circulating tumor DNA more than three years prior to clinical diagnosis, and provide benchmark sensitivities required for this purpose.","PeriodicalId":9430,"journal":{"name":"Cancer discovery","volume":"3 1","pages":""},"PeriodicalIF":29.7000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer discovery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1158/2159-8290.cd-25-0375","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
To explore how early can cancers be detected prior to clinical signs or symptoms, we assessed prospectively collected serial plasma samples from the Atherosclerosis Risk in Communities (ARIC) study, including 26 participants diagnosed with cancer and 26 matched controls. At the index time point, eight of these 52 participants scored positively with a multicancer early detection (MCED) test. All eight participants were diagnosed with cancer within 4 months after blood collection. In six of these 8 participants, we were able to assess an earlier plasma sample collected 3.1 to 3.5 years prior to clinical diagnosis. In four of these six participants, the same mutations detected by the MCED test could be identified, but at 8.6 to 79-fold lower mutant allele fractions. These results demonstrate that it is possible to detect circulating tumor DNA more than three years prior to clinical diagnosis, and provide benchmark sensitivities required for this purpose.
期刊介绍:
Cancer Discovery publishes high-impact, peer-reviewed articles detailing significant advances in both research and clinical trials. Serving as a premier cancer information resource, the journal also features Review Articles, Perspectives, Commentaries, News stories, and Research Watch summaries to keep readers abreast of the latest findings in the field. Covering a wide range of topics, from laboratory research to clinical trials and epidemiologic studies, Cancer Discovery spans the entire spectrum of cancer research and medicine.