PMID- 36230609 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240417 IS - 2072-6694 (Print) IS - 2072-6694 (Electronic) IS - 2072-6694 (Linking) VI - 14 IP - 19 DP - 2022 Sep 26 TI - Cross-Domain Text Mining to Predict Adverse Events from Tyrosine Kinase Inhibitors for Chronic Myeloid Leukemia. LID - 10.3390/cancers14194686 [doi] LID - 4686 AB - Tyrosine kinase inhibitors (TKIs) are prescribed for chronic myeloid leukemia (CML) and some other cancers. The objective was to predict and rank TKI-related adverse events (AEs), including under-reported or preclinical AEs, using novel text mining. First, k-means clustering of 2575 clinical CML TKI abstracts separated TKIs by significant (p < 0.05) AE type: gastrointestinal (bosutinib); edema (imatinib); pulmonary (dasatinib); diabetes (nilotinib); cardiovascular (ponatinib). Next, we propose a novel cross-domain text mining method utilizing a knowledge graph, link prediction, and hub node network analysis to predict new relationships. Cross-domain text mining of 30+ million articles via SemNet predicted and ranked known and novel TKI AEs. Three physiology-based tiers were formed using unsupervised rank aggregation feature importance. Tier 1 ranked in the top 1%: hematology (anemia, neutropenia, thrombocytopenia, hypocellular marrow); glucose (diabetes, insulin resistance, metabolic syndrome); iron (deficiency, overload, metabolism), cardiovascular (hypertension, heart failure, vascular dilation); thyroid (hypothyroidism, hyperthyroidism, parathyroid). Tier 2 ranked in the top 5%: inflammation (chronic inflammatory disorder, autoimmune, periodontitis); kidney (glomerulonephritis, glomerulopathy, toxic nephropathy). Tier 3 ranked in the top 10%: gastrointestinal (bowel regulation, hepatitis, pancreatitis); neuromuscular (autonomia, neuropathy, muscle pain); others (secondary cancers, vitamin deficiency, edema). Results suggest proactive TKI patient AE surveillance levels: regular surveillance for tier 1, infrequent surveillance for tier 2, and symptom-based surveillance for tier 3. FAU - Mehra, Nidhi AU - Mehra N AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. FAU - Varmeziar, Armon AU - Varmeziar A AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. FAU - Chen, Xinyu AU - Chen X AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. FAU - Kronick, Olivia AU - Kronick O AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. FAU - Fisher, Rachel AU - Fisher R AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. FAU - Kota, Vamsi AU - Kota V AUID- ORCID: 0000-0002-5290-9289 AD - Division of Hematology and Oncology, Georgia Cancer Center, Augusta University, Augusta, GA 30912, USA. FAU - Mitchell, Cassie S AU - Mitchell CS AD - Laboratory for Pathology Dynamics, Department of Biomedical Engineering, Georgia Institute of Technology, Emory University School of Medicine, Atlanta, GA 30332, USA. AD - Center for Machine Learning, Georgia Institute of Technology, Atlanta, GA 30332, USA. LA - eng GR - R21 CA232249/CA/NCI NIH HHS/United States GR - R21CA232249/NH/NIH HHS/United States PT - Journal Article DEP - 20220926 PL - Switzerland TA - Cancers (Basel) JT - Cancers JID - 101526829 PMC - PMC9563938 OTO - NOTNLM OT - BCR ABL OT - adverse event OT - chronic myeloid leukemia OT - heterogeneous information network OT - machine learning OT - natural language processing OT - side effect OT - toxicity OT - tyrosine kinase inhibitor COIS- The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. EDAT- 2022/10/15 06:00 MHDA- 2022/10/15 06:01 PMCR- 2022/09/26 CRDT- 2022/10/14 01:51 PHST- 2022/07/26 00:00 [received] PHST- 2022/09/04 00:00 [revised] PHST- 2022/09/23 00:00 [accepted] PHST- 2022/10/14 01:51 [entrez] PHST- 2022/10/15 06:00 [pubmed] PHST- 2022/10/15 06:01 [medline] PHST- 2022/09/26 00:00 [pmc-release] AID - cancers14194686 [pii] AID - cancers-14-04686 [pii] AID - 10.3390/cancers14194686 [doi] PST - epublish SO - Cancers (Basel). 2022 Sep 26;14(19):4686. doi: 10.3390/cancers14194686.