| Literature DB >> 32590103 |
Shengda Luo1, Jiahui Xu2, Zebo Jiang2, Lei Liu1, Qibiao Wu3, Elaine Lai-Han Leung4, Alex Po Leung5.
Abstract
In personalized medicine, many factors influence the choice of compounds. Hence, the selection of suitable medicine for patients with non-small-cell lung cancer (NSCLC) is expensive. To shorten the decision-making process for compounds, we propose a computationally efficient and cost-effective collaborative filtering method with ensemble learning. The ensemble learning is used to handle small-sample sizes in drug response datasets as the typical number of patients in a cancer dataset is very small. Moreover, the proposed method can be used to identify the most suitable compounds for patients without genetic data. To the best of our knowledge, this is the first method to provide effective recommendations without genetic data. We also constructed a reliable dataset that includes eight NSCLC cell lines and ten compounds that have been approved by the Food and Drug Administration. With the new dataset, the experimental results demonstrated that the dataset shift phenomenon that commonly occurs in practical biomedical data does not occur in this problem. The experimental results demonstrated that our proposed method can outperform two state-of-the-art recommender system techniques on both the NCI60 dataset and our new dataset. Our model can be applied to the prediction of drug sensitivity with less labor-intensive experiments in the future.Entities:
Keywords: Ensemble learning; Non-small-cell lung cancer; Personalized medicine; Recommender system
Year: 2020 PMID: 32590103 DOI: 10.1016/j.phrs.2020.105037
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658