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A metabolite-based liquid biopsy for detection of ovarian cancer.
Fahrmann, Johannes F; Ghasemi, Seyyed Mahmood; Han, Chae Y; Wu, Ranran; Dennison, Jennifer B; Vykoukal, Jody; Celestino, Joseph; Lu, Karen; Lu, Zhen; Drescher, Charles; Do, Kim-Anh; Hanash, Samir; Bast, Robert C; Irajizad, Ehsan.
Affiliation
  • Fahrmann JF; Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Ghasemi SM; Department of Biostatistics, The University of Texas M.D. Anderson Cancer Center, 6767 Bertner Street, Houston, TX, 77030, USA.
  • Han CY; Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
  • Wu R; Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Dennison JB; Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Vykoukal J; Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Celestino J; Department of Gynecological Oncology and Reproductive Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
  • Lu K; Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
  • Lu Z; Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
  • Drescher C; Translational Research Program, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Do KA; Division of Gynecologic Oncology, Swedish Cancer Institute, Seattle, WA, USA.
  • Hanash S; Department of Biostatistics, The University of Texas M.D. Anderson Cancer Center, 6767 Bertner Street, Houston, TX, 77030, USA.
  • Bast RC; Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
  • Irajizad E; Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
Biomark Res ; 12(1): 91, 2024 Aug 28.
Article in En | MEDLINE | ID: mdl-39192316
ABSTRACT
Serial CA125 and second line transvaginal ultrasound (TVS) screening in the UKCTOCS indicated a shift towards detection of earlier stage ovarian cancer (OvCa), but did not yield a significant mortality reduction. There remains a need to establish additional biomarkers that can complement CA125 for even earlier and at a larger proportion of new cases. Using a cohort of plasma samples from 219 OvCa cases (59 stage I/II and 160 stage III/IV) and 409 female controls and a novel Sensitivity Maximization At A Given Specificity (SMAGS) method, we developed a blood-based metabolite-based test consisting of 7 metabolites together with CA125 for detection of OvCa. At a 98.5% specificity cutpoint, the metabolite test achieved sensitivity of 86.2% for detection of early-stage OvCa and was able to capture 64% of the cases with low CA125 levels (< 35 units/mL). In an independent test consisting of 65 early-stage OvCa cases and 141 female controls, the metabolite panel achieved sensitivity of 73.8% at a 91.4% specificity and captured 13 (44.8%) out of 29 early-stage cases with CA125 levels < 35 units/mL. The metabolite test has utility for ovarian cancer screening, capable of improving upon CA125 for detection of early-stage disease.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biomark Res Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biomark Res Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom