硼替佐米
多发性骨髓瘤
地塞米松
药品
价值(数学)
集合(抽象数据类型)
医学
计算机科学
计算生物学
生物信息学
肿瘤科
药理学
机器学习
内科学
生物
程序设计语言
作者
Ashmita Bose,Peter Dittrich,Jerzy Górecki
标识
DOI:10.3389/fchem.2022.901918
摘要
It can be expected that medical treatments in the future will be individually tailored for each patient. Here we present a step towards personally addressed drug therapy. We consider multiple myeloma treatment with drugs: bortezomib and dexamethasone. It has been observed that these drugs are effective for some patients and do not help others. We describe a network of chemical oscillators that can help to differentiate between non-responsive and responsive patients. In our numerical simulations, we consider a network of 3 interacting oscillators described with the Oregonator model. The input information is the gene expression value for one of 15 genes measured for patients with multiple myeloma. The single-gene networks optimized on a training set containing outcomes of 239 therapies, 169 using bortezomib and 70 using dexamethasone, show up to 71% accuracy in differentiating between non-responsive and responsive patients. If the results of single-gene networks are combined into the concilium with the majority voting strategy, then the accuracy of predicting the patient’s response to the therapy increases to ∼ 85%.
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