Please use this identifier to cite or link to this item: https://hdl.handle.net/1/223
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dc.contributor.authorMollee, P.en
dc.contributor.authorTiley, Campbellen
dc.contributor.authorCunningham, I.en
dc.contributor.authorMoore, J.en
dc.contributor.authorPrince, M.en
dc.contributor.authorCannell, P.en
dc.contributor.authorGibbons, S.en
dc.contributor.authorTate, J.en
dc.contributor.authorPaul, S.en
dc.contributor.authorMar Fan, H.en
dc.contributor.authorGill, Devinder Sen
dc.date.accessioned2015-04-15T01:03:17Zen
dc.date.available2015-04-15T01:03:17Zen
dc.date.issued2012-06en
dc.identifier.citationVolume 157, Issue 6, pp. 766-769en
dc.identifier.issn1365-2141en
dc.identifier.urihttps://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/223en
dc.description.abstractFirst Paragraph: Melphalan is a cornerstone of treatment for AL amyloidosis. Intravenous (IV) melphalan is used for patients suitable for autologous stem cell transplantation (ASCT), while oral mel- phalan and dexamethasone is standard treatment for patients unsuited for intensive therapy. IV melphalan, however, may have some advantages in non-ASCT eligible patients with AL amyloidosis, based on unpredictable oral absorption (Bo- sanquet & Gilby, 1984) and theoretical concern that gastroin- testinal involvement may further impair absorption (Sattianayagam et al, 2009).en
dc.subjectCanceren
dc.subjectDrug Therapyen
dc.titleA Phase II Study of Risk-Adapted Intravenous Melphalan in patients with AL Amyloidosisen
dc.typeJournal Articleen
dc.identifier.doi10.1111/j.1365-2141.2012.09080.xen
dc.description.pubmedurihttp://www.ncbi.nlm.nih.gov/pubmed/22390735en
dc.identifier.journaltitleBritish Journal of Haematologyen
dc.type.studyortrialClinical Trialen
dc.originaltypeTexten
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptHaematology-
Appears in Collections:Oncology / Cancer
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