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ABSTRACT: Background
Bosutinib, a tyrosine kinase inhibitor (TKI), is effective in treating chronic myeloid leukemia (CML) patients resistant or intolerant to previous TKIs. Unlike other TKIs, bosutinib's lack of inhibition of c-KIT and PDGFR may contribute to its unique tolerability profile. Similar to dasatinib, it targets Bcr/Abl and SRC kinases, particularly Lyn, raising safety concerns. In fact, the susceptibility of Lyn -/- mice to autoimmune disorders and the deregulation of Lyn-dependent pathways in patients with lupus were previously shown.Aims
This study aimed to assess the time-adjusted rate (TAR) of inflammatory/immune-related adverse events in bosutinib-treated patients.Methods
We analyzed clinical data from 60 patients with a minimum follow-up of three months. W
SUBMITTER: Agostani E
PROVIDER: S-EPMC11799592 | biostudies-literature | 2025 Feb
REPOSITORIES: biostudies-literature