Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23481
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dc.contributor.authorRobinson, Danielle H-
dc.contributor.authorHughes, Charlotte F M-
dc.contributor.authorGrigg, Andrew P-
dc.date2020-05-30-
dc.date.accessioned2020-06-10T00:47:13Z-
dc.date.available2020-06-10T00:47:13Z-
dc.date.issued2020-10-
dc.identifier.citationLeukemia & lymphoma 2020; 61(10): 2448-2452-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23481-
dc.description.abstractCyclosporin is an immunosuppressive agent in allogeneic hematopoietic stem cell transplantation and its metabolism is strongly affected by concomitant drugs, including posaconazole which is now extensively used as anti-fungal prophylaxis post-allograft. We undertook a retrospective audit of 29 patients undergoing their first allograft who were receiving posaconazole at the time of transition from intravenous to oral cyclosporin. This group had a median initial oral cyclosporin dose of 2.58 mg/kg bd (range 1.75-3.95) and high incidence of cyclosporin-related toxicity was noted, requiring significant dose reductions such that by day 60 the media dose was 1.60 mg/kg bd (range 0.86-3.33). We subsequently amended our dosing protocol and analyzed a further 20 patients specifying an initial oral cyclosporin dose of 2.25 mg/kg bd and found this had little impact on toxicity or requirement for dose reductions. Starting doses of no greater than 2 mg/kg bd appear optimal to prevent toxicity in allograft recipients receiving concomitant posaconazole.-
dc.language.isoeng-
dc.subjectTransplantation-
dc.subjectcyclosporin-
dc.subjectdrug toxicity-
dc.subjectposaconazole-
dc.titleOptimal oral cyclosporin dosing with concomitant posaconazole post allogeneic stem cell transplantation.-
dc.typeJournal Article-
dc.identifier.journaltitleLeukemia & lymphoma-
dc.identifier.affiliationDepartment of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1080/10428194.2020.1768381-
dc.identifier.orcid0000-0001-9809-6757en
dc.identifier.orcid0000-0003-0384-704Xen
dc.identifier.pubmedid32476517-
dc.type.austinJournal Article-
local.name.researcherGrigg, Andrew P
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptClinical Haematology-
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