A method for correlating the clinical outcome of a patient suffering from or at risk of developing gynecologic cancer with the presence or non-presence of a defect in expression of at least one gene selected from the group comprising ALCAM, Osteopontin, Her-2/neu, EGFR, uPA/PAI-1 and/or ESRI, said method comprising the steps of:
- a) obtaining a (fixed) biological sample from said patient;
- b) determining the expression level of at least one of the said marker genes in said patient according to any of the above methods;
- and
- c) correlating the pattern of expression level(s) determined in (b) with said patient's data, said data being selected from the group consisting of etiopathology data, clinical symptoms, anamnesis data and/or data concerning the therapeutic regimen.