Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18074
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dc.contributor.authorGleeson, M-
dc.contributor.authorCounsell, Nicholas-
dc.contributor.authorCunningham, D-
dc.contributor.authorChadwick, N-
dc.contributor.authorLawrie, A-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorMcMillan, A-
dc.contributor.authorArdeshna, K M-
dc.contributor.authorJack, A-
dc.contributor.authorSmith, P-
dc.contributor.authorMouncey, P-
dc.contributor.authorPocock, C-
dc.contributor.authorRadford, J A-
dc.contributor.authorDavies, J-
dc.contributor.authorTurner, D-
dc.contributor.authorKruger, A-
dc.contributor.authorJohnson, P-
dc.contributor.authorGambell, J-
dc.contributor.authorLinch, D-
dc.date.accessioned2018-07-10T06:36:54Z-
dc.date.available2018-07-10T06:36:54Z-
dc.date.issued2017-10-01-
dc.identifier.citationAnnals of Oncology: Official Journal of the European Society for Medical Oncology 2017; 28(10): 2511-2516en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18074-
dc.description.abstractCentral nervous system (CNS) relapse of diffuse large B-cell lymphoma (DLBCL) is associated with a dismal prognosis. Here, we report an analysis of CNS relapse for patients treated within the UK NCRI phase III R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone) 14 versus 21 randomised trial. The R-CHOP 14 versus 21 trial compared R-CHOP administered two- versus three weekly in previously untreated patients aged ≥18 years with bulky stage I-IV DLBCL (n = 1080). Details of CNS prophylaxis were retrospectively collected from participating sites. The incidence and risk factors for CNS relapse including application of the CNS-IPI were evaluated. 177/984 patients (18.0%) received prophylaxis (intrathecal (IT) methotrexate (MTX) n = 163, intravenous (IV) MTX n = 2, prophylaxis type unknown n = 11 and IT MTX and cytarabine n = 1). At a median follow-up of 6.5 years, 21 cases of CNS relapse (isolated n = 11, with systemic relapse n = 10) were observed, with a cumulative incidence of 1.9%. For patients selected to receive prophylaxis, the incidence was 2.8%. Relapses predominantly involved the brain parenchyma (81.0%) and isolated leptomeningeal involvement was rare (14.3%). Univariable analysis demonstrated the following risk factors for CNS relapse: performance status 2, elevated lactate dehydrogenase, IPI, >1 extranodal site of disease and presence of a 'high-risk' extranodal site. Due to the low number of events no factor remained significant in multivariate analysis. Application of the CNS-IPI revealed a high-risk group (4-6 risk factors) with a 2- and 5-year incidence of CNS relapse of 5.2% and 6.8%, respectively. Despite very limited use of IV MTX as prophylaxis, the incidence of CNS relapse following R-CHOP was very low (1.9%) confirming the reduced incidence in the rituximab era. The CNS-IPI identified patients at highest risk for CNS recurrence. ISCRTN number 16017947 (R-CHOP14v21); EudraCT number 2004-002197-34.en_US
dc.language.isoeng-
dc.subjectcentral nervous systemen_US
dc.subjectdiffuse large B-cell lymphomaen_US
dc.subjectrelapseen_US
dc.subjectrituximaben_US
dc.titleCentral nervous system relapse of diffuse large B-cell lymphoma in the rituximab era: results of the UK NCRI R-CHOP-14 versus 21 trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAnnals of Oncology: Official Journal of the European Society for Medical Oncologyen_US
dc.identifier.affiliationDepartment of Medicine, The Royal Marsden Hospital, London and Surrey, UKen_US
dc.identifier.affiliationCancer Research UK and UCL Cancer Trials Centre, UCL Cancer Institute, London, UKen_US
dc.identifier.affiliationMedical Oncologyen_US
dc.identifier.affiliationDepartment of Medical Oncology, Eastern Health, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Haematology, Nottingham City Hospital, Nottingham, UKen_US
dc.identifier.affiliationDepartment of Haematology, University College London, London, UKen_US
dc.identifier.affiliationDepartment of Haematology, Mount Vernon Cancer Centre, Northwood, UKen_US
dc.identifier.affiliationHMDS, Leeds Teaching Hospitals NHS Trust, Leeds, UKen_US
dc.identifier.affiliationDepartment of Haematology, East Kent Hospitals, Canterbury, UKen_US
dc.identifier.affiliationThe University of Manchester and The Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UKen_US
dc.identifier.affiliationDepartment of Haematology, Western General Hospital, Edinburgh, UKen_US
dc.identifier.affiliationDepartment of Haematology, Torbay Hospital, Torquay, UKen_US
dc.identifier.affiliationDepartment of Haematology, Royal Cornwall Hospital, Truro, UKen_US
dc.identifier.affiliationCancer Research UK Centre, Southampton, UKen_US
dc.identifier.affiliationClinical Haematologyen_US
dc.identifier.doi10.1093/annonc/mdx353en_US
dc.type.contentTexten_US
dc.identifier.pubmedid28961838-
dc.type.austinClinical Trial, Phase III-
dc.type.austinJournal Article-
dc.type.austinRandomized Controlled Trial-
local.name.researcherHawkes, Eliza A
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.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptInfectious Diseases-
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