Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16187
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dc.contributor.authorDouglas, Genevieve-
dc.contributor.authorHarrison, Claire-
dc.contributor.authorForsyth, Cecily J-
dc.contributor.authorBennett, Michael R-
dc.contributor.authorStevenson, William-
dc.contributor.authorHounsell, John-
dc.contributor.authorRatnasingam, Sumita-
dc.contributor.authorRitchie, David-
dc.contributor.authorRoss, David M-
dc.contributor.authorGrigg, Andrew P-
dc.date2016-07-25-
dc.date.accessioned2016-09-06T01:59:52Z-
dc.date.available2016-09-06T01:59:52Z-
dc.date.issued2017-01-
dc.identifier.citationLeukemia & Lymphoma 2017; 58(1): 89-95en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16187-
dc.description.abstractHydroxyurea (Hu) is widely used as first-line cytoreductive therapy for patients with high-risk Philadelphia-negative myeloproliferative neoplasms (Ph-neg MPN), but a small proportion of patients have refractory disease or experience adverse effects. Studies have demonstrated busulfan (Bu) to be an active first-line agent, but data on its role as second-line or later therapy are minimal. To evaluate its efficacy and safety in this context, we undertook a multicenter audit of Ph-neg MPN patients who had received Bu as therapy for Hu intolerance or failure. Of 51 patients identified, 38 (75%) achieved either complete or partial hematological response following at least one Bu cycle. Bu was generally well tolerated, with only 21/135 (15%) cycles complicated by adverse effects, predominantly cytopenia; only 6% of cycles were ceased due to treatment complications. Bu is an effective and well-tolerated agent in patients with Ph-neg MPN in the setting of Hu intolerance or unresponsiveness.en_US
dc.subjectPhiladelphia-negative myeloproliferative neoplasmsen_US
dc.subjectBusulfanen_US
dc.subjectHydroxyureaen_US
dc.titleBusulfan is effective second-line therapy for older patients with Philadelphia-negative myeloproliferative neoplasms intolerant of or unresponsive to hydroxyureaen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleLeukemia & Lymphomaen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Clinical Haematology, Austin Hospital, University of Melbourne, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Haematology, Guys and St Thomas' NHS Foundation Trust, London, UKen_US
dc.identifier.affiliationWyong Hospital, Hamlyn Terrace, NSW, Australiaen_US
dc.identifier.affiliationRoyal North Shore Hospital, Sydney, NSW, Australiaen_US
dc.identifier.affiliationWarrnambool Base Hospital, Warrnambool, Victoria, Australiaen_US
dc.identifier.affiliationRoyal Melbourne Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationFlinders University, Adelaide, SA, Australiaen_US
dc.identifier.affiliationFlinders Medical Centre, Adelaide, SA, Australiaen_US
dc.identifier.affiliationSA Pathology, Adelaide, SA, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27454522en_US
dc.identifier.doi10.1080/10428194.2016.1187269en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherDouglas, Genevieve
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptClinical Haematology-
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