3.8 Article

Conformal predictors in early diagnostics of ovarian and breast cancers

Journal

PROGRESS IN ARTIFICIAL INTELLIGENCE
Volume 1, Issue 3, Pages 245-257

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s13748-012-0021-y

Keywords

Proteomics; Mass spectrometry; Artificial intelligence; Prediction with confidence; Early diagnosis; Conformal predictors; Ovarian cancer; Breast cancer; Biological markers

Funding

  1. MRC
  2. Medical Research Council
  3. Cancer Research UK
  4. Department of Health
  5. UCLH
  6. Eve Appeal
  7. Bart's
  8. EraSysBio+ grant funds from the European Union
  9. BBSRC
  10. BMBF Living with uninvited guests: comparing plant and animal responses to endocytic invasions
  11. MRC Grant [G0802594, G0301107]
  12. EU FP7 grant O-PTM-Biomarkers (2008-2011)
  13. Grant 'Development of new Venn prediction methods for osteoporosis risk assessment' from the Cyprus Research Promotion Foundation
  14. BBSRC [BB/I004548/1] Funding Source: UKRI
  15. MRC [G0301107, G0801228, G0802594, G9901012, G0401619] Funding Source: UKRI

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The work describes an application of a recently developed machine-learning technique called Mondrian predictors to risk assessment of ovarian and breast cancers. The analysis is based on mass spectrometry profiling of human serum samples that were collected in the United Kingdom Collaborative Trial of Ovarian Cancer Screening. The work describes the technique and presents the results of classification (diagnosis) and the corresponding measures of confidence of the diagnostics. The main advantage of this approach is a proven validity of prediction. The work also describes an approach to improve early diagnosis of ovarian and breast cancers since the data in the United Kingdom Collaborative Trial of Ovarian Cancer Screening were collected over a period of 7 years and do allow to make observations of changes in human serum over that period of time. Significance of improvement is confirmed statistically (for up to 11 months for ovarian cancer and 9 months for breast cancer). In addition, the methodology allowed us to pinpoint the same mass spectrometry peaks as previously detected as carrying statistically significant information for discrimination between healthy and diseased patients. The results are discussed.

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