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https://ahro.austin.org.au/austinjspui/handle/1/18074
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DC Field | Value | Language |
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dc.contributor.author | Gleeson, M | - |
dc.contributor.author | Counsell, Nicholas | - |
dc.contributor.author | Cunningham, D | - |
dc.contributor.author | Chadwick, N | - |
dc.contributor.author | Lawrie, A | - |
dc.contributor.author | Hawkes, Eliza A | - |
dc.contributor.author | McMillan, A | - |
dc.contributor.author | Ardeshna, K M | - |
dc.contributor.author | Jack, A | - |
dc.contributor.author | Smith, P | - |
dc.contributor.author | Mouncey, P | - |
dc.contributor.author | Pocock, C | - |
dc.contributor.author | Radford, J A | - |
dc.contributor.author | Davies, J | - |
dc.contributor.author | Turner, D | - |
dc.contributor.author | Kruger, A | - |
dc.contributor.author | Johnson, P | - |
dc.contributor.author | Gambell, J | - |
dc.contributor.author | Linch, D | - |
dc.date.accessioned | 2018-07-10T06:36:54Z | - |
dc.date.available | 2018-07-10T06:36:54Z | - |
dc.date.issued | 2017-10-01 | - |
dc.identifier.citation | Annals of Oncology: Official Journal of the European Society for Medical Oncology 2017; 28(10): 2511-2516 | en_US |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/18074 | - |
dc.description.abstract | Central 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.iso | eng | - |
dc.subject | central nervous system | en_US |
dc.subject | diffuse large B-cell lymphoma | en_US |
dc.subject | relapse | en_US |
dc.subject | rituximab | en_US |
dc.title | Central 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.type | Journal Article | en_US |
dc.identifier.journaltitle | Annals of Oncology: Official Journal of the European Society for Medical Oncology | en_US |
dc.identifier.affiliation | Department of Medicine, The Royal Marsden Hospital, London and Surrey, UK | en_US |
dc.identifier.affiliation | Cancer Research UK and UCL Cancer Trials Centre, UCL Cancer Institute, London, UK | en_US |
dc.identifier.affiliation | Medical Oncology | en_US |
dc.identifier.affiliation | Department of Medical Oncology, Eastern Health, Melbourne, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Nottingham City Hospital, Nottingham, UK | en_US |
dc.identifier.affiliation | Department of Haematology, University College London, London, UK | en_US |
dc.identifier.affiliation | Department of Haematology, Mount Vernon Cancer Centre, Northwood, UK | en_US |
dc.identifier.affiliation | HMDS, Leeds Teaching Hospitals NHS Trust, Leeds, UK | en_US |
dc.identifier.affiliation | Department of Haematology, East Kent Hospitals, Canterbury, UK | en_US |
dc.identifier.affiliation | The University of Manchester and The Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK | en_US |
dc.identifier.affiliation | Department of Haematology, Western General Hospital, Edinburgh, UK | en_US |
dc.identifier.affiliation | Department of Haematology, Torbay Hospital, Torquay, UK | en_US |
dc.identifier.affiliation | Department of Haematology, Royal Cornwall Hospital, Truro, UK | en_US |
dc.identifier.affiliation | Cancer Research UK Centre, Southampton, UK | en_US |
dc.identifier.affiliation | Clinical Haematology | en_US |
dc.identifier.doi | 10.1093/annonc/mdx353 | en_US |
dc.type.content | Text | en_US |
dc.identifier.pubmedid | 28961838 | - |
dc.type.austin | Clinical Trial, Phase III | - |
dc.type.austin | Journal Article | - |
dc.type.austin | Randomized Controlled Trial | - |
local.name.researcher | Hawkes, Eliza A | |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Clinical Haematology | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Infectious Diseases | - |
Appears in Collections: | Journal articles |
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