Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33808
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dc.contributor.authorReynolds, Gemma-
dc.contributor.authorUrbancic, Karen F-
dc.contributor.authorFong, Chun Y-
dc.contributor.authorTrubiano, Jason-
dc.date2023-
dc.date.accessioned2023-09-27T05:36:40Z-
dc.date.available2023-09-27T05:36:40Z-
dc.date.issued2023-11-
dc.identifier.citationBritish Journal of Haematology 2023-11; 203(4)en_US
dc.identifier.issn1365-2141-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33808-
dc.description.abstractThe co-administration of venetoclax, a BCL-2 inhibitor, with a mould-active azole, such a posaconazole, has potential to both prevent invasive fungal infection (IFI) and reduce the required treatment dose, and cost, of venetoclax. Posaconazole drug-level monitoring is critical to ensuring adequate mould prophylaxis. A retrospective audit of 99 patients at a tertiary cancer centre, with myeloid malignancies co-prescribed venetoclax and posaconazole between January 2018 and April 2022, was undertaken to evaluate the adequacy of posaconazole prescribing and the rate of breakthrough IFI. Seventy-six patients (77%) had at least one posaconazole level measured in the study period, with 37% requiring a dose adjustment based on steady-state trough levels. Breakthrough IFI occurred in 4% of patients, typically within 1 month of commencing anti-mould prophylaxis. Close monitoring of posaconazole levels in venetoclax-treated patients, particularly in the early, outpatient setting, is critical.en_US
dc.language.isoeng-
dc.subjectBCL-2en_US
dc.subjectMDSen_US
dc.subjectantifungalen_US
dc.subjectfungal infectionen_US
dc.subjectinfectionen_US
dc.titleInvasive fungal infection following venetoclax and posaconazole co-administration.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBritish Journal of Haematologyen_US
dc.identifier.affiliationInfectious Diseasesen_US
dc.identifier.affiliationPharmacyen_US
dc.identifier.affiliationClinical Haematologyen_US
dc.identifier.affiliationNational Centre for Infections in Cancer, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.;Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.1111/bjh.19116en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-9561-3592en_US
dc.identifier.orcid0000-0002-9275-578Xen_US
dc.identifier.orcid0000-0001-5773-103Xen_US
dc.identifier.orcid0000-0002-5111-6367en_US
dc.identifier.pubmedid37731068-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptPharmacy-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCentre for Antibiotic Allergy and Research-
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