Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32259
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dc.contributor.authorArulogun, Suzanne O-
dc.contributor.authorBrian, Duncan-
dc.contributor.authorGoradia, Harshita-
dc.contributor.authorCooney, Aaron-
dc.contributor.authorMenne, Tobias-
dc.contributor.authorKoo, RayMun-
dc.contributor.authorO'Neill, Aideen T-
dc.contributor.authorVos, Josephine M I-
dc.contributor.authorPratt, Guy-
dc.contributor.authorTurner, Deborah-
dc.contributor.authorMarshall, Kirsty-
dc.contributor.authorManos, Kate-
dc.contributor.authorAnderson, Claire-
dc.contributor.authorGavriatopoulou, Maria-
dc.contributor.authorKyriakou, Charalampia-
dc.contributor.authorKersten, Marie J-
dc.contributor.authorMinnema, Monique C-
dc.contributor.authorKoutoumanou, Eirini-
dc.contributor.authorEl-Sharkawi, Dima-
dc.contributor.authorLinton, Kim-
dc.contributor.authorTalaulikar, Dipti-
dc.contributor.authorMcCarthy, Helen-
dc.contributor.authorBishton, Mark-
dc.contributor.authorFollows, George-
dc.contributor.authorWechalekar, Ashutosh-
dc.contributor.authorD'Sa, Shirley P-
dc.date2023-
dc.date.accessioned2023-03-08T01:06:36Z-
dc.date.available2023-03-08T01:06:36Z-
dc.date.issued2023-03-03-
dc.identifier.citationAmerican Journal of Hematology 2023; 98(5)en_US
dc.identifier.issn1096-8652-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32259-
dc.description.abstractBendamustine and rituximab (BR) therapy is commonly used in the treatment of Waldenström Macroglobulinaemia (WM). The impact dose of Bendamustine dose on response and survival outcomes is not well established, and the impact of its use in different treatment settings is not clear. We aimed to report response rates and survival outcomes following BR, and clarify the impact of depth of response and bendamustine dose on survival. A total of 250 WM patients treated with BR in the frontline or relapsed settings were included in this multicentre, retrospective cohort analysis. Rates of partial response (PR) or better differed significantly between the frontline and relapsed cohorts (91.4% vs 73.9%, respectively; p<0.001). Depth of response impacted survival outcomes: two-year predicted PFS rates after achieving CR/VGPR vs PR were 96% vs 82%, respectively (p=0.002). Total bendamustine dose was predictive of PFS: in the frontline setting, PFS was superior in the group receiving ≥1000mg/m2 compared with those receiving 800-999mg/m2 (p=0.04). In the relapsed cohort, those who received doses of <600mg/m2 had poorer PFS outcomes compared with those who received ≥600mg/m2 (p=0.02). Attaining CR/VGPR following BR results in superior survival, and total bendamustine dose significantly impacts response and survival outcomes, in both frontline and relapsed settings. This article is protected by copyright. All rights reserved.en_US
dc.language.isoeng-
dc.titleBendamustine plus rituximab for the treatment of Waldenström Macroglobulinaemia: patient outcomes and impact of bendamustine dosing.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAmerican Journal of Hematologyen_US
dc.identifier.affiliationUniversity Colleg, London Hospitals NHS Foundation Trust, London, United Kingdom.en_US
dc.identifier.affiliationAddenbrooke's Hospital, Cambridge, United Kingdom.en_US
dc.identifier.affiliationNottingham University Hospitals, Nottingham, United Kingdom.en_US
dc.identifier.affiliationUniversity Hospitals Dorset NHS Foundation Trust, Bournemouth, United Kingdom.en_US
dc.identifier.affiliationFreeman Hospital, Newcastle Hospitals NHS Foundation Trust, United Kingdom.en_US
dc.identifier.affiliationDepartment of Haematology, ACT Pathology, Canberra Health Services, Canberra, Australia.en_US
dc.identifier.affiliationAmsterdam UMC location University of Amsterdam, Department of Hematology & LYMMCARE, Amsterdam, the Netherlands.en_US
dc.identifier.affiliationQueen Elizabeth Hospital, Birmingham, United Kingdom.en_US
dc.identifier.affiliationTorbay and South Devon NHS Foundation Trust, Torbay, United Kingdom.en_US
dc.identifier.affiliationThe Royal Marsden NHS Foundation Trust, London, United Kingdom.en_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationBarnet and Chase Farm NHS Hospitals Trust, London, United Kingdom.en_US
dc.identifier.affiliationAlexandra Hospital, Athens, Greece.en_US
dc.identifier.affiliationUniversity Medical Center Utrecht, Utrecht, Netherlands.en_US
dc.identifier.affiliationGreat Ormond Street Institute of Child Health, University College London, United Kingdom.en_US
dc.identifier.affiliationThe Christie NHS Foundation Trust, Manchester, United Kingdom.en_US
dc.identifier.affiliationUniversity Hospitals Dorset NHS Foundation Trust, Bournemouth, United Kingdom.en_US
dc.identifier.affiliationTranslational Medical Sciences, University of Nottingham, Nottingham, United Kingdom.en_US
dc.identifier.affiliationAddenbrooke's Hospital, Cambridge, United Kingdom.en_US
dc.identifier.doi10.1002/ajh.26895en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-5151-4990en_US
dc.identifier.orcid0000-0002-3139-8379en_US
dc.identifier.orcid0000-0001-6058-1036en_US
dc.identifier.pubmedid36866925-
local.name.researcherManos, Kate
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptClinical Haematology-
Appears in Collections:Journal articles
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