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Towards realizing the vision of precision medicine: AI based prediction of clinical drug response.
de Jong, Johann; Cutcutache, Ioana; Page, Matthew; Elmoufti, Sami; Dilley, Cynthia; Fröhlich, Holger; Armstrong, Martin.
Afiliação
  • de Jong J; Data and Translational Sciences, UCB Biosciences GmbH, 40789 Monheim am Rhein, Germany.
  • Cutcutache I; Data and Translational Sciences, UCB Pharma, Slough SL1 3WE, UK.
  • Page M; Data and Translational Sciences, UCB Pharma, Slough SL1 3WE, UK.
  • Elmoufti S; Late Development Statistics, UCB Biosciences Inc., Raleigh, NC 27617, USA.
  • Dilley C; Head of Asset Strategy, UCB Inc., Smyrna, GA 30080, USA.
  • Fröhlich H; Data and Translational Sciences, UCB Biosciences GmbH, 40789 Monheim am Rhein, Germany.
  • Armstrong M; Fraunhofer Institute for Scientific Computing and Algorithms (SCAI), Business Area Bioinformatics, 53757 Sankt Augustin, Germany.
Brain ; 144(6): 1738-1750, 2021 07 28.
Article em En | MEDLINE | ID: mdl-33734308
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirrolidinonas / Simulação por Computador / Medicina de Precisão / Aprendizado de Máquina / Anticonvulsivantes Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirrolidinonas / Simulação por Computador / Medicina de Precisão / Aprendizado de Máquina / Anticonvulsivantes Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2021 Tipo de documento: Article