Outcomes of COVID-19 in patients with CLL: a multicenter international experience. Academic Article uri icon

Overview

abstract

  • 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.

authors

  • Mato, Anthony R
  • Roeker, Lindsey E
  • Lamanna, Nicole
  • Allan, John
  • Leslie, Lori
  • Pagel, John M
  • Patel, Krish
  • Osterborg, Anders
  • Wojenski, Daniel
  • Kamdar, Manali
  • Huntington, Scott F
  • Davids, Matthew S
  • Brown, Jennifer R
  • Antic, Darko
  • Jacobs, Ryan
  • Ahn, Inhye E
  • Pu, Jeffrey
  • Isaac, Krista M
  • Barr, Paul M
  • Ujjani, Chaitra S
  • Geyer, Mark B
  • Berman, Ellin
  • Zelenetz, Andrew D
  • Malakhov, Nikita
  • Furman, Richard R
  • Koropsak, Michael
  • Bailey, Neil
  • Hanson, Lotta
  • Perini, Guilherme F
  • Ma, Shuo
  • Ryan, Christine E
  • Wiestner, Adrian
  • Portell, Craig A
  • Shadman, Mazyar
  • Chong, Elise A
  • Brander, Danielle M
  • Sundaram, Suchitra
  • Seddon, Amanda N
  • Seymour, Erlene
  • Patel, Meera
  • Martinez-Calle, Nicolas
  • Munir, Talha
  • Walewska, Renata
  • Broom, Angus
  • Walter, Harriet
  • El-Sharkawi, Dima
  • Parry, Helen
  • Wilson, Matthew R
  • Patten, Piers E M
  • Hernández-Rivas, José-Ángel
  • Miras, Fatima
  • Fernández Escalada, Noemi
  • Ghione, Paola
  • Nabhan, Chadi
  • Lebowitz, Sonia
  • Bhavsar, Erica
  • López-Jiménez, Javier
  • Naya, Daniel
  • Garcia-Marco, Jose Antonio
  • Skånland, Sigrid S
  • Cordoba, Raul
  • Eyre, Toby A

publication date

  • September 3, 2020

Research

keywords

  • Coronavirus Infections
  • Leukemia, Lymphocytic, Chronic, B-Cell
  • Pneumonia, Viral

Identity

PubMed Central ID

  • PMC7472711

Scopus Document Identifier

  • 85089864394

Digital Object Identifier (DOI)

  • 10.1182/blood.2020006965

PubMed ID

  • 32688395

Additional Document Info

volume

  • 136

issue

  • 10