Efficacy and safety of isavuconazole compared with voriconazole as primary antifungal prophylaxis in allogeneic hematopoietic cell transplant recipients.
Isavuconazole
allogeneic hematopoietic cell transplant
invasive fungal infections
prophylaxis
voriconazole
Journal
Medical mycology
ISSN: 1460-2709
Titre abrégé: Med Mycol
Pays: England
ID NLM: 9815835
Informations de publication
Date de publication:
04 Oct 2021
04 Oct 2021
Historique:
received:
10
12
2020
accepted:
15
05
2021
revised:
10
02
2021
pubmed:
27
5
2021
medline:
18
1
2022
entrez:
26
5
2021
Statut:
ppublish
Résumé
Voriconazole is frequently discontinued prematurely as primary antifungal prophylaxis (AFP) in allogeneic hematopoietic cell transplant (HCT) recipients due to adverse events. Limited data exists for isavuconazole as AFP. We analyzed adult HCT recipients who received voriconazole or isavuconazole AFP to estimate rate of premature AFP discontinuation, identify risk factors for premature AFP discontinuation, and compare incidence of invasive fungal infection (IFI) and survival at day + 180 post-HCT between patients who received voriconazole/isavuconazole-AFP. This was a propensity score matched cohort analysis of 210 HCT-recipients who received voriconazole-AFP (9/1/2014-12/31/2016; voriconazole-cohort), and 95 HCT-recipients who received isavuconazole-AFP (5/1/2017-10/31/2018; isavuconazole-cohort). AFP discontinuation for any reason prior to completion was defined as "premature". Median (interquartile range, IQR) duration of AFP was longer in the isavuconazole-cohort (94 days, 87-100) vs. the voriconazole-cohort (76 days, 23-94; P-value < 0.0001). Premature AFP discontinuation was more frequent in the voriconazole-cohort (92/210, 43.8%) vs. the isavuconazole-cohort (14/95, 14.7%; P-value < 0.0001). The most common reason for premature discontinuation was biochemical hepatotoxicity (voriconazole-cohort: 48/210, 22.8% vs. isavuconazole-cohort: 5/95, 5.26%; P-value = 0.0002). Transaminase values between baseline and end-of-treatment (EOT) and up to 14 days post-EOT significantly increased in the voriconazole-cohort, but remained unchanged in the isavuconazole-cohort. The incidence of IFI at day + 180 was 2.9% (6/210) and 3.2% (3/95) in the voriconazole-cohort and isavuconazole-cohort, respectively (P-value = 0.881). All-cause mortality at day + 180 was 2.4% (5/210) and 6.3% (6/95) in the voriconazole-cohort and isavuconazole-cohort, respectively (P-value = 0.089). When compared to voriconazole, isavuconazole was a safer and as effective primary AFP during the first 3 months after HCT. When compared to voriconazole, isavuconazole is a safer and as effective primary antifungal prophylaxis during the first 3 months after allogeneic hematopoietic cell transplant, with lower rates of hepatotoxicity, and similar rates of fungal infections and all-cause mortality.
Identifiants
pubmed: 34036319
pii: 6283791
doi: 10.1093/mmy/myab025
pmc: PMC8487767
doi:
Substances chimiques
Antifungal Agents
0
Nitriles
0
Pyridines
0
Triazoles
0
isavuconazole
60UTO373KE
Voriconazole
JFU09I87TR
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
970-979Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
Pays : United States
Organisme : NIH HHS
ID : P30 CA008748
Pays : United States
Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology.
Références
Clin Infect Dis. 2018 Oct 30;67(10):1610-1613
pubmed: 29771293
Mycoses. 2019 Aug;62(8):665-672
pubmed: 31050373
N Engl J Med. 2007 Jan 25;356(4):348-59
pubmed: 17251531
Clin Infect Dis. 2020 Feb 14;70(5):723-730
pubmed: 30958538
Bone Marrow Transplant. 1995 Jun;15(6):825-8
pubmed: 7581076
N Engl J Med. 2007 Jan 25;356(4):335-47
pubmed: 17251530
Mycoses. 2019 Jun;62(6):534-541
pubmed: 30851214
Biol Blood Marrow Transplant. 2010 Jan;16(1):46-52
pubmed: 20053331
Clin Infect Dis. 2021 May 18;72(10):1755-1763
pubmed: 32236406
Clin Infect Dis. 2019 May 30;68(12):1981-1989
pubmed: 30289478
Biol Blood Marrow Transplant. 2008 Jun;14(6):641-50
pubmed: 18489989
Med Mycol. 2020 Nov 10;58(8):1029-1036
pubmed: 32171012
J Infect. 2014 Oct;69(4):341-351
pubmed: 24931578
Lancet. 2016 Feb 20;387(10020):760-9
pubmed: 26684607
Med Mycol. 2020 Jun 1;58(4):417-424
pubmed: 31613363
Blood. 2010 Dec 9;116(24):5111-8
pubmed: 20826719
Bone Marrow Transplant. 2016 Jul;51(7):1010-2
pubmed: 26974271
Biol Blood Marrow Transplant. 2009 Oct;15(10):1143-238
pubmed: 19747629
Biol Blood Marrow Transplant. 2020 Jun;26(6):1195-1202
pubmed: 32088367
J Natl Compr Canc Netw. 2016 Jul;14(7):882-913
pubmed: 27407129
Mycoses. 2019 Jan;62(1):81-86
pubmed: 30230043
Biol Blood Marrow Transplant. 2011 Oct;17(10):1460-71
pubmed: 21310254
J Antimicrob Chemother. 2018 Mar 1;73(3):757-763
pubmed: 29194488
Leuk Lymphoma. 2015 Mar;56(3):663-70
pubmed: 24913499
Clin Infect Dis. 2008 Jun 15;46(12):1813-21
pubmed: 18462102
Clin Infect Dis. 2018 Oct 30;67(10):1621-1630
pubmed: 29860307
Mycoses. 2018 Nov;61(11):868-876
pubmed: 30035825