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Network-based machine learning approach to predict immunotherapy response in cancer patients

DC Field Value Language
dc.contributor.authorKong, JungHo-
dc.contributor.authorHa, Doyeon-
dc.contributor.authorLee, Juhun-
dc.contributor.authorKim, Inhae-
dc.contributor.authorPark, Minhyuk-
dc.contributor.authorIm, Sin-Hyeog-
dc.contributor.authorShin, Kunyoo-
dc.contributor.authorKim, Sanguk-
dc.date.accessioned2022-10-11T00:25:55Z-
dc.date.available2022-10-11T00:25:55Z-
dc.date.created2022-09-27-
dc.date.created2022-09-27-
dc.date.issued2022-06-
dc.identifier.citationNature Communications, Vol.13, p. 3703-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://hdl.handle.net/10371/185644-
dc.description.abstractImmune checkpoint inhibitors (ICIs) have substantially improved the survival of cancer patients over the past several years. However, only a minority of patients respond to ICI treatment (similar to 30% in solid tumors), and current ICI-response-associated biomarkers often fail to predict the ICI treatment response. Here, we present a machine learning (ML) framework that leverages network-based analyses to identify ICI treatment biomarkers (NetBio) that can make robust predictions. We curate more than 700 ICI-treated patient samples with clinical outcomes and transcriptomic data, and observe that NetBio-based predictions accurately predict ICI treatment responses in three different cancer types-melanoma, gastric cancer, and bladder cancer. Moreover, the NetBio-based prediction is superior to predictions based on other conventional ICI treatment biomarkers, such as ICI targets or tumor microenvironment-associated markers. This work presents a network-based method to effectively select immunotherapy-response-associated biomarkers that can make robust ML-based predictions for precision oncology.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleNetwork-based machine learning approach to predict immunotherapy response in cancer patients-
dc.typeArticle-
dc.identifier.doi10.1038/s41467-022-31535-6-
dc.citation.journaltitleNature Communications-
dc.identifier.wosid000820251300008-
dc.identifier.scopusid2-s2.0-85133007975-
dc.citation.startpage3703-
dc.citation.volume13-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorShin, Kunyoo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusTUMOR-
dc.subject.keywordPlusBLOCKADE-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusNIVOLUMAB-
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