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Deep reinforcement learning for personalized treatment recommendation
Author(s) -
Liu Mingyang,
Shen Xiaotong,
Pan Wei
Publication year - 2022
Publication title -
statistics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.996
H-Index - 183
eISSN - 1097-0258
pISSN - 0277-6715
DOI - 10.1002/sim.9491
Subject(s) - reinforcement learning , computer science , machine learning , personalized medicine , artificial intelligence , ranking (information retrieval) , precision medicine , recommender system , markov decision process , supervised learning , learning to rank , process (computing) , markov process , artificial neural network , bioinformatics , medicine , mathematics , statistics , pathology , biology , operating system
In precision medicine, the ultimate goal is to recommend the most effective treatment to an individual patient based on patient‐specific molecular and clinical profiles, possibly high‐dimensional. To advance cancer treatment, large‐scale screenings of cancer cell lines against chemical compounds have been performed to help better understand the relationship between genomic features and drug response; existing machine learning approaches use exclusively supervised learning, including penalized regression and recommender systems. However, it would be more efficient to apply reinforcement learning to sequentially learn as data accrue, including selecting the most promising therapy for a patient given individual molecular and clinical features and then collecting and learning from the corresponding data. In this article, we propose a novel personalized ranking system called Proximal Policy Optimization Ranking (PPORank), which ranks the drugs based on their predicted effects per cell line (or patient) in the framework of deep reinforcement learning (DRL). Modeled as a Markov decision process, the proposed method learns to recommend the most suitable drugs sequentially and continuously over time. As a proof‐of‐concept, we conduct experiments on two large‐scale cancer cell line data sets in addition to simulated data. The results demonstrate that the proposed DRL‐based PPORank outperforms the state‐of‐the‐art competitors based on supervised learning. Taken together, we conclude that novel methods in the framework of DRL have great potential for precision medicine and should be further studied.

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