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ABSTRACT: Background
Large cell transformation (LCT) of Sezary Syndrome (SS) is a rare phenomenon. To date, there are no rigorous studies identifying risk factors for its development.Objectives
Here, we seek to characterize the clinicopathologic risk factors that predispose patients with SS to develop LCT.Methods
We retrospectively evaluated all SS patient records available in the Michigan Medicine Cancer Registry from 2010-2021. Clinical and pathologic variables were compared between groups. The Kaplan-Meier method and log-rank test were used to assess overall survival.Results
Of 28 SS patients identified, eight patients experienced LCT, and 20 did not (NLCT). Peak lactate dehydrogenase (LDH) before LCT (p = 0.0012), maximum total body surface area (TBSA) involvement
SUBMITTER: Jairath NK
PROVIDER: S-EPMC9668185 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature