| Literature DB >> 33283555 |
Eric J Chow1,2,3, David R Doody1, Jennifer J Wilkes2, Laura K Becker4, Shasank Chennupati1, Pamela E Morin4, Lena E Winestone5, Henry J Henk3, Gary H Lyman1,6.
Abstract
With tyrosine kinase inhibitor (TKI) therapy, chronic myelogenous leukemia (CML) is now a chronic disease. CML patients treated with TKIs (n = 1200) were identified from the OptumLabs® Data Warehouse (de-identified claims and electronic health records) between 2000 and 2016 and compared with a non-cancer cohort (n = 7635). The 5-year cumulative incidence of all organ system outcomes was significantly greater for the TKI versus non-cancer group. In the first year, compared with imatinib, later generation TKIs were associated with primary infections (hazard ratios [HR] 1.43, 95% CI 1.02-2.00), circulatory events (HR 1.15, 95% CI 1.01-1.31), and skin issues (HR 1.43, 95% CI 1.13-1.80); musculoskeletal and nervous system/sensory issues were less common (HRs 0.83-0.84, p < 0.05). Increased risk of infections, cardiopulmonary and skin issues associated with later generation TKIs persisted in subsequent years. In this real-world population, TKI therapy was associated with a high burden of adverse events. Later generation TKIs may have greater toxicity than imatinib.Entities:
Keywords: Chronic myelogenous leukemia; complications; epidemiology; insurance; tyrosine kinase inhibitor
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Year: 2020 PMID: 33283555 PMCID: PMC8106632 DOI: 10.1080/10428194.2020.1855340
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022