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Outcomes of COVID-19 in patients with CLL: a multicenter international experience
Author(s) -
Anthony R. Mato,
Lindsey E. Roeker,
Nicole Lamanna,
John N. Allan,
Lori A. Leslie,
John M. Pagel,
Krish Patel,
Anders Österborg,
Daniel Wojenski,
Manali Kamdar,
Scott F. Huntington,
Matthew S. Davids,
Jennifer R. Brown,
Darko Antić,
Ryan Jacobs,
Inhye E. Ahn,
Jeffrey J. Pu,
Krista M. Isaac,
Paul M. Barr,
Chaitra S. Ujjani,
Mark B. Geyer,
Ellin Berman,
Andrew D. Zelenetz,
Nikita Malakhov,
Richard R. Furman,
Michael Koropsak,
Neil A. Bailey,
Lotta Hanson,
Guilherme Fleury Perini,
Shuo Ma,
Christine E. Ryan,
Adrian Wiestner,
Craig A. Portell,
Mazyar Shadman,
Elise A. Chong,
Danielle M. Brander,
Suchitra Sundaram,
Amanda N. Seddon,
Erlene Seymour,
Meera Patel,
Nicolás MartínezCalle,
Talha Munir,
Renata Walewska,
Angus Broom,
Harriet S. Walter,
Dima ElSharkawi,
Helen Parry,
Matthew R. Wilson,
Piers Patten,
JoséÁngel HernándezRivas,
Fatima Mirás,
Noemi Fernández Escalada,
Paola Ghione,
Chadi Nabhan,
Sonia Lebowitz,
Erica B. Bhavsar,
Javier LópezJiménez,
Daniel E. Naya,
José A. GarcíaMarco,
Sigrid S. Skånland,
Raúl Córdoba,
Toby A. Eyre
Publication year - 2020
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood.2020006965
Subject(s) - medicine , case fatality rate , chronic lymphocytic leukemia , comorbidity , pediatrics , epidemiology , leukemia
Given advanced age, comorbidities, and immune dysfunction, chronic lymphocytic leukemia (CLL) patients may be at particularly high risk of infection and poor outcomes related to coronavirus disease 2019 (COVID-19). Robust analysis of outcomes for CLL patients, particularly examining effects of baseline characteristics and CLL-directed therapy, is critical to optimally manage CLL patients through this evolving pandemic. CLL patients diagnosed with symptomatic COVID-19 across 43 international centers (n = 198) were included. Hospital admission occurred in 90%. Median age at COVID-19 diagnosis was 70.5 years. Median Cumulative Illness Rating Scale score was 8 (range, 4-32). Thirty-nine percent were treatment naive ("watch and wait"), while 61% had received ≥1 CLL-directed therapy (median, 2; range, 1-8). Ninety patients (45%) were receiving active CLL therapy at COVID-19 diagnosis, most commonly Bruton tyrosine kinase inhibitors (BTKi's; n = 68/90 [76%]). At a median follow-up of 16 days, the overall case fatality rate was 33%, though 25% remain admitted. Watch-and-wait and treated cohorts had similar rates of admission (89% vs 90%), intensive care unit admission (35% vs 36%), intubation (33% vs 25%), and mortality (37% vs 32%). CLL-directed treatment with BTKi's at COVID-19 diagnosis did not impact survival (case fatality rate, 34% vs 35%), though the BTKi was held during the COVID-19 course for most patients. These data suggest that the subgroup of CLL patients admitted with COVID-19, regardless of disease phase or treatment status, are at high risk of death. Future epidemiologic studies are needed to assess severe acute respiratory syndrome coronavirus 2 infection risk, these data should be validated independently, and randomized studies of BTKi's in COVID-19 are needed to provide definitive evidence of benefit.

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