A fuzzy measurement-based assessment of breast cancer prognostic markers

被引：11

作者：

Seker, H ^{[1
]}

Odetayo, M ^{[1
]}

Petrovic, D ^{[1
]}

Naguib, RNG ^{[1
]}

Bartoli, C ^{[1
]}

Alasio, L ^{[1
]}

Lakshmi, MS ^{[1
]}

Sherbet, GV ^{[1
]}

机构：

[1] Coventry Univ, Biomed Comp Res Grp, BIOCORE, Sch Math & Informat Sci, Coventry CV1 5FB, W Midlands, England

来源：

2000 IEEE EMBS INTERNATIONAL CONFERENCE ON INFORMATION TECHNOLOGY APPLICATIONS IN BIOMEDICINE, PROCEEDINGS | 2000年

关键词：

oncology; predictive analysis; artificial intelligence; soft feature subset selection; survival analysis;

D O I：

10.1109/ITAB.2000.892381

中图分类号：

TP39 [计算机的应用];

学科分类号：

081203 ; 0835 ;

摘要：

This paper aims to assess breast cancer prognostic markers and to determine an optimum subset that can yield high prediction accuracy for an individual breast cancer patient's prognosis by means of a fuzzy measurement derived from the fuzzy k-nearest neighbour algorithm (FK-NN). The analyses are carried out for both nodal involvement and five-year survival. The data set used for the analysis of breast cancer prognosis consists of seven input markers (Histology type, Grade, DNA ploidy, S-Phase Fraction (SPF), G(0)G(1)/G(2)M Ratio, minimum and maximum Nuclear Pleomorphism Indices (NPI)) and two corresponding outputs to be predicted (negative or positive nodal status in the case of nodal involvement assessment, and whether the patient is alive or dead within 5 years of diagnosis for survival analysis). The highest predictive accuracy is 78% with the fuzzy measurement of 0.7254 for nodal involvement assessment, and 88% with the fuzzy measurement of 0.8183 for survival analysis. The best results are obtained from the subset {Histology type, Grade, DNA ploidy, SPF (%), G(0)G(1)/G(2)M Ratio} for survival prediction and the subset {Grade, SPF, minimum NPI} for nodal involvement analysis.

引用

页码：174 / 178

页数：5

共 4 条

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KELLER, JM ;

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[2]

Naguib R N, 1999, IEEE Trans Inf Technol Biomed, V3, P61, DOI 10.1109/4233.748976

[3]

SEKER H, 2000, IN PRESS INT S COMP

[4]

SEKER H, 2000, IN PRESS WORLD C MED

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