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A personalized probabilistic approach to ovarian cancer diagnostics.
Ban, Dongjo; Housley, Stephen N; Matyunina, Lilya V; McDonald, L DeEtte; Bae-Jump, Victoria L; Benigno, Benedict B; Skolnick, Jeffrey; McDonald, John F.
Afiliación
  • Ban D; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA.
  • Housley SN; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA.
  • Matyunina LV; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA.
  • McDonald LD; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA.
  • Bae-Jump VL; Department of Obstetrics and Gynecology, University of North Carolina, 3009 Old Clinic Building, Chapel Hill, NC 27599, USA.
  • Benigno BB; Ovarian Cancer Institute, 1266 W. Paces Ferry Rd NW #339, Atlanta, GA 30327, USA.
  • Skolnick J; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA; Ovarian Cancer Institute, 1266 W. Paces Ferry Rd NW #339, Atlanta, GA 30327, USA; Center for the Study of Systems Biology, School of Biological Sciences, Georgi
  • McDonald JF; Integrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332, USA. Electronic address: john.mcdonald@biology.gatech.edu.
Gynecol Oncol ; 182: 168-175, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38266403
ABSTRACT

OBJECTIVE:

The identification/development of a machine learning-based classifier that utilizes metabolic profiles of serum samples to accurately identify individuals with ovarian cancer.

METHODS:

Serum samples collected from 431 ovarian cancer patients and 133 normal women at four geographic locations were analyzed by mass spectrometry. Reliable metabolites were identified using recursive feature elimination coupled with repeated cross-validation and used to develop a consensus classifier able to distinguish cancer from non-cancer. The probabilities assigned to individuals by the model were used to create a clinical tool that assigns a likelihood that an individual patient sample is cancer or normal.

RESULTS:

Our consensus classification model is able to distinguish cancer from control samples with 93% accuracy. The frequency distribution of individual patient scores was used to develop a clinical tool that assigns a likelihood that an individual patient does or does not have cancer.

CONCLUSIONS:

An integrative approach using metabolomic profiles and machine learning-based classifiers has been employed to develop a clinical tool that assigns a probability that an individual patient does or does not have ovarian cancer. This personalized/probabilistic approach to cancer diagnostics is more clinically informative and accurate than traditional binary (yes/no) tests and represents a promising new direction in the early detection of ovarian cancer.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans Idioma: En Revista: Gynecol Oncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans Idioma: En Revista: Gynecol Oncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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