Clinical features associated with COVID-19 outcome in multiple myeloma: first results from the International Myeloma Society data set.
Journal
Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509
Informations de publication
Date de publication:
24 12 2020
24 12 2020
Historique:
received:
21
07
2020
accepted:
17
09
2020
entrez:
28
12
2020
pubmed:
29
12
2020
medline:
6
1
2021
Statut:
ppublish
Résumé
The primary cause of morbidity and mortality in patients with multiple myeloma (MM) is an infection. Therefore, there is great concern about susceptibility to the outcome of COVID-19-infected patients with MM. This retrospective study describes the baseline characteristics and outcome data of COVID-19 infection in 650 patients with plasma cell disorders, collected by the International Myeloma Society to understand the initial challenges faced by myeloma patients during the COVID-19 pandemic. Analyses were performed for hospitalized MM patients. Among hospitalized patients, the median age was 69 years, and nearly all patients (96%) had MM. Approximately 36% were recently diagnosed (2019-2020), and 54% of patients were receiving first-line therapy. Thirty-three percent of patients have died, with significant geographic variability, ranging from 27% to 57% of hospitalized patients. Univariate analysis identified age, International Staging System stage 3 (ISS3), high-risk disease, renal disease, suboptimal myeloma control (active or progressive disease), and 1 or more comorbidities as risk factors for higher rates of death. Neither history of transplant, including within a year of COVID-19 diagnosis, nor other anti-MM treatments were associated with outcomes. Multivariate analysis found that only age, high-risk MM, renal disease, and suboptimal MM control remained independent predictors of adverse outcome with COVID-19 infection. The management of MM in the era of COVID-19 requires careful consideration of patient- and disease-related factors to decrease the risk of acquiring COVID-19 infection, while not compromising disease control through appropriate MM treatment. This study provides initial data to develop recommendations for the management of MM patients with COVID-19 infection.
Identifiants
pubmed: 33367546
pii: S0006-4971(20)83904-4
doi: 10.1182/blood.2020008150
pmc: PMC7759145
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3033-3040Subventions
Organisme : NCI NIH HHS
ID : P01 CA155258
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA100707
Pays : United States
Références
Leukemia. 2020 Aug;34(8):2173-2183
pubmed: 32546725
Transplant Proc. 2020 Sep;52(7):2178-2185
pubmed: 32217016
Lancet. 2020 Jun 20;395(10241):1919-1926
pubmed: 32473682
Lancet Glob Health. 2020 Aug;8(8):e1003-e1017
pubmed: 32553130
Haematologica. 2015 Jan;100(1):107-13
pubmed: 25344526
Blood. 2019 Feb 14;133(7):621
pubmed: 30587526
Nat Rev Clin Oncol. 2012 Feb 21;9(3):135-43
pubmed: 22349016
Science. 2020 Jul 10;369(6500):208-211
pubmed: 32404476
Blood Cancer J. 2020 Oct 19;10(10):103
pubmed: 33077708
Nat Med. 2020 Aug;26(8):1218-1223
pubmed: 32581323
Leukemia. 2020 Aug;34(8):2000-2011
pubmed: 32444866
Br J Haematol. 2007 Sep;138(5):563-79
pubmed: 17686051
Lancet. 2020 Jun 20;395(10241):1907-1918
pubmed: 32473681
JAMA Oncol. 2020 Sep 1;6(9):1471-1472
pubmed: 32614417
Haematologica. 2020 Jun 05;105(9):e480-483
pubmed: 33054068
J Hematol Oncol. 2020 Jul 14;13(1):94
pubmed: 32664919
Lancet Oncol. 2020 Jul;21(7):893-903
pubmed: 32479790
JAMA. 2020 May 12;323(18):1775-1776
pubmed: 32203977
Nat Microbiol. 2020 Apr;5(4):536-544
pubmed: 32123347
Cancer J. 2019 Jan/Feb;25(1):45-53
pubmed: 30694859
Nat Rev Immunol. 2020 Jul;20(7):448
pubmed: 32533107