Abstract

We present a novel, cost efficient two-phase design for predictive clinical gene expression studies: early marker panel determination (EMPD). In Phase-1, genome-wide microarrays are used only for a small number of individual patient samples. From this Phase-1 data a panel of marker genes is derived. In Phase-2, the expression values of these marker panel genes are measured for a large group of patients and a predictive classification model is learned from this data. Phase-2 does not require the use of expensive whole genome microarrays, thus making EMPD a cost efficient alternative for current trials. The expected performance loss of EMPD is compared to designs which use genome-wide microarrays for all patients. We also examine the trade-off between the number of patients included in Phase-1 and the number of marker genes required in Phase-2. By analysis of five published datasets we find that in Phase-1 already 16 patients per group are sufficient to determine a suitable marker panel of 10 genes, and that this early decision compromises the final performance only marginally.

Submitted: November 4, 2004 · Accepted: March 18, 2005 · Published: April 26, 2005

Recommended Citation

Jaeger, Jochen; Weichenhan, Dieter; Ivandic, Boris; and Spang, Rainer (2005) "Early Diagnostic Marker Panel Determination for Microarray Based Clinical Studies," Statistical Applications in Genetics and Molecular Biology: Vol. 4 : Iss. 1, Article 9.
DOI: 10.2202/1544-6115.1109
Available at: http://www.bepress.com/sagmb/vol4/iss1/art9