Towards realizing the vision of precision medicine: AI based prediction of clinical drug response

Author:

de Jong Johann1ORCID,Cutcutache Ioana2,Page Matthew2,Elmoufti Sami3,Dilley Cynthia4,Fröhlich Holger156,Armstrong Martin7

Affiliation:

1. Data and Translational Sciences, UCB Biosciences GmbH, 40789 Monheim am Rhein, Germany

2. Data and Translational Sciences, UCB Pharma, Slough SL1 3WE, UK

3. Late Development Statistics, UCB Biosciences Inc., Raleigh, NC 27617, USA

4. Head of Asset Strategy, UCB Inc., Smyrna, GA 30080, USA

5. Fraunhofer Institute for Scientific Computing and Algorithms (SCAI), Business Area Bioinformatics, 53757 Sankt Augustin, Germany

6. Bonn-Aachen International Center for IT, University of Bonn, 53115 Bonn, Germany

7. Data and Translational Sciences, UCB Pharma, 1420 Braine l’Alleud, Belgium

Abstract

Abstract Accurate and individualized prediction of response to therapies is central to precision medicine. However, because of the generally complex and multifaceted nature of clinical drug response, realizing this vision is highly challenging, requiring integrating different data types from the same individual into one prediction model. We used the anti-epileptic drug brivaracetam as a case study and combine a hybrid data/knowledge-driven feature extraction with machine learning to systematically integrate clinical and genetic data from a clinical discovery dataset (n = 235 patients). We constructed a model that successfully predicts clinical drug response [area under the curve (AUC) = 0.76] and show that even with limited sample size, integrating high-dimensional genetics data with clinical data can inform drug response prediction. After further validation on data collected from an independently conducted clinical study (AUC = 0.75), we extensively explore our model to gain insights into the determinants of drug response, and identify various clinical and genetic characteristics predisposing to poor response. Finally, we assess the potential impact of our model on clinical trial design and demonstrate that, by enriching for probable responders, significant reductions in clinical study sizes may be achieved. To our knowledge, our model represents the first retrospectively validated machine learning model linking drug mechanism of action and the genetic, clinical and demographic background in epilepsy patients to clinical drug response. Hence, it provides a blueprint for how machine learning-based multimodal data integration can act as a driver in achieving the goals of precision medicine in fields such as neurology.

Funder

UCB Pharma

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Reference90 articles.

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