Incidence of breakthrough fungal infections on isavuconazole prophylaxis compared to posaconazole and voriconazole

被引:11
|
作者
Scott, Sara A. [1 ,3 ]
Perry, Cory [1 ]
Mahmoudjafari, Zahra [1 ]
Martin, Grace A. [1 ]
Boyd, Samuel [2 ]
Thompson, Jeffrey [2 ]
Thomas, Beth [1 ]
机构
[1] Univ Kansas Hlth Syst, Dept Pharm, Kansas City, KS USA
[2] Univ Kansas, Dept Biostat & Data Sci, Med Ctr, Kansas City, KS USA
[3] Univ Kansas Hlth Syst, Dept Pharm, 4000 Cambridge St, Kansas City, KS 66160 USA
关键词
acute myeloid leukemia; alloHSCT; AML; fungal prophylaxis; isavuconazole; posaconazole; stem cell transplant; voriconazole; PRIMARY ANTIFUNGAL PROPHYLAXIS; FLUCONAZOLE; TRIAL;
D O I
10.1111/tid.14045
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Invasive fungal infections (IFIs) are a common infectious complication during the treatment of acute myeloid leukemia (AML), high-risk myelodysplastic syndrome (MDS) or post hematopoietic cell transplantation (HCT). For these patients, the National Comprehensive Cancer Network recommends posaconazole or voriconazole for IFI prophylaxis. In clinical practice, however, there has been increased use of isavuconazole due to favorable pharmacokinetic and pharmacodynamic parameters despite limited data for this indication. The comparative prophylactic efficacy of antifungals in this patient population has not been reported, and an analysis is warranted.Methods: This retrospective, matched cohort, single-center study, included AML, MDS, or HCT patients who began treatment or underwent transplant between January 1, 2015 and July 31, 2021. Isavuconazole patients were matched 1:2 with patients receiving posaconazole or voriconazole prophylaxis.Results: A total of 126 patients were included, 42 received isavuconazole, 81 received posaconazole, and three received voriconazole. The majority of patients were male receiving secondary IFI prophylaxis while receiving steroids for treatment of GVHD. The incidence of possible, probable or proven IFI was 16.7% in the isavuconazole group compared to 10.7% in the posaconazole and voriconazole group (OR 1.28, 95% CI -0.9-1.4; p = .67). Hepatotoxicity occurred in 16 total patients, 14 receiving posaconazole and two receiving isavuconazole.Conclusion: Patients who received isavuconazole prophylaxis during AML induction therapy or post-HCT experienced a similar incidence of breakthrough fungal infections compared to those who received posaconazole or voriconazole. These results suggest no difference in antifungal prophylactic efficacy; however larger prospective comparative studies are needed.
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