Limits of Predictive Models Using Microarray Data for Breast Cancer Clinical Treatment Outcome

التفاصيل البيبلوغرافية
العنوان: Limits of Predictive Models Using Microarray Data for Breast Cancer Clinical Treatment Outcome
المؤلفون: Maria Grazia Daidone, Lara Lusa, Loris De Cecco, James F. Reid, Danila Coradini, Silvia Veneroni, Manuela Gariboldi, Marco A. Pierotti
المصدر: JNCI: Journal of the National Cancer Institute. 97:927-930
بيانات النشر: Oxford University Press (OUP), 2005.
سنة النشر: 2005
مصطلحات موضوعية: Adult, Genetic Markers, Oncology, Cancer Research, medicine.medical_specialty, Breast Neoplasms, Biology, Logistic regression, Bioinformatics, Breast cancer, Predictive Value of Tests, Internal medicine, Biomarkers, Tumor, Odds Ratio, medicine, Humans, Aged, Oligonucleotide Array Sequence Analysis, Homeodomain Proteins, Models, Statistical, Receptors, Interleukin-17, Reverse Transcriptase Polymerase Chain Reaction, Microarray analysis techniques, Gene Expression Profiling, Reproducibility of Results, Receptors, Interleukin, Odds ratio, Middle Aged, medicine.disease, Confidence interval, Logistic Models, Treatment Outcome, ROC Curve, Sample size determination, Area Under Curve, Predictive value of tests, Mann–Whitney U test, Female
الوصف: Data from microarray studies have been used to develop predictive models for treatment outcome in breast cancer, such as a recently proposed predictive model for antiestrogen response after tamoxifen treatment that was based on the expression ratio of two genes. We attempted to validate this model on an independent cohort of 58 patients with resectable estrogen receptor-positive breast cancer. We measured expression of the genes HOXB13 and IL17BR with real time-quantitative polymerase chain reaction and assessed the association between their expression and outcome by use of univariate logistic regression, area under the receiver-operating-characteristic curve (AUC), a two-sample t test, and a Mann-Whitney test. We also applied standard supervised methods to the original microarray dataset and to another independent dataset from similar patients to estimate the classification accuracy obtainable by using more than two genes in a microarray-based predictive model. We could not validate the performance of the two-gene predictor on our cohort of samples (relation between outcome and the following genes estimated by logistic regression: for HOXB13, odds ratio [OR] = 1.04, 95% confidence interval [CI] = 0.92 to 1.16, P = .54; for IL17BR, OR = 0.69, 95% CI = 0.40 to 1.20, P = .18; and for HOXB13/IL17BR, OR = 1.30, 95% CI = 0.88 to 1.93, P = .18). Similar results were obtained with the AUC, a two-sample two-sided t test, and a Mann-Whitney test. In addition, estimates of classification accuracies applied to two independent microarray datasets highlighted the poor performance of treatment-response predictive models that can be achieved with the sample sizes of patients and informative genes to date.
تدمد: 1460-2105
0027-8874
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f8643e6e91b41f079dff604b0719da0Test
https://doi.org/10.1093/jnci/dji153Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....3f8643e6e91b41f079dff604b0719da0
قاعدة البيانات: OpenAIRE