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Although many biomarkers linked to SRL response have been identified, there is no consensus criterion on how to assign this pharmacologic treatment according to biomarker levels. Our aim is to provide better predictive tools for an accurate acromegaly patient stratification regarding the ability to respond to SRL. We took advantage of a multicenter study of 71 acromegaly patients and we used advanced mathematical modelling to predict SRL response combining molecular and clinical information. Different models of patient stratification were obtained, with a much higher accuracy when the studied cohort is fragmented according to relevant clinical characteristics. Considering all the models, a patient stratification based on the extrasellar growth of the tumor, sex, age and the expression of E-cadherin,\n                    <jats:italic>GHRL<\/jats:italic>\n                    ,\n                    <jats:italic>IN1-GHRL<\/jats:italic>\n                    ,\n                    <jats:italic>DRD2<\/jats:italic>\n                    ,\n                    <jats:italic>SSTR5<\/jats:italic>\n                    and\n                    <jats:italic>PEBP1<\/jats:italic>\n                    is proposed, with accuracies that stand between 71 to 95%. In conclusion, the use of data mining could be very useful for implementation of personalized medicine in acromegaly through an interdisciplinary work between computer science, mathematics, biology and medicine. 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