Abstract
Sézary syndrome (SS) is an aggressive cutaneous T-cell lymphoma with poor survival. We performed a retrospective review of SS patients at Emory University from 1990 to 2020. We collected data on race, clinical characteristics, therapy, and social determinants of health. Clinical endpoints were overall survival (OS) and time to next treatment (TTNT). Univariate association and multivariable analyses were assessed by Cox proportional hazards models. Among 62 patients, 45.2% were AA. The median OS and TTNT were 3.1 years and 6.3 months, respectively, with no difference by race. AA patients had a higher median baseline LDH (360 vs. 232, p = 0.002) and a longer delay in initiation of systemic therapy compared to CC patients (3.17 vs. 2.14 months, p = 0.039), but a shorter commute (<10 miles) and no difference in insurance coverage (p = 0.260). AA patients at an academic center had unique clinical features and treatment patterns, but similar survival to CC SS patients.
Ethical approval
This study was reviewed and approved by IRB; approval # 0001489.
Presentations
Data presented in this manuscript were published as an abstract at the 2020 American Society of Hematology Annual Meeting.
Disclosure statement
DJM, SG, and JS report no conflicts, MJL reports advisory board and honorarium from Kyowa Kirin, and PBA reports advisory board and research funding from Kyowa Kirin.
Data availability statement
Data were available within the article or its supplementary materials.