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dc.contributor.authorGleeson, M
dc.contributor.authorCounsell, N
dc.contributor.authorCunningham, D
dc.contributor.authorChadwick, N
dc.contributor.authorLawrie, A
dc.contributor.authorHawkes, EA
dc.contributor.authorMcMillan, A
dc.contributor.authorArdeshna, KM
dc.contributor.authorJack, A
dc.contributor.authorSmith, P
dc.contributor.authorMouncey, P
dc.contributor.authorPocock, C
dc.contributor.authorRadford, JA
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.accessioned2017-07-26T14:33:55Z
dc.date.issued2017-10
dc.identifier.citationAnnals of oncology : official journal of the European Society for Medical Oncology, 2017, 28 (10), pp. 2511 - 2516
dc.identifier.issn0923-7534
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/745
dc.identifier.eissn1569-8041
dc.identifier.doi10.1093/annonc/mdx353
dc.description.abstractBackground 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.Patients and methods 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.Results 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.Conclusion 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.Clinicaltrials.gov ISCRTN number 16017947 (R-CHOP14v21); EudraCT number 2004-002197-34.
dc.formatPrint
dc.format.extent2511 - 2516
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.subjectHumans
dc.subjectCentral Nervous System Neoplasms
dc.subjectNeoplasm Recurrence, Local
dc.subjectCyclophosphamide
dc.subjectVincristine
dc.subjectDoxorubicin
dc.subjectPrednisone
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectDrug Administration Schedule
dc.subjectProspective Studies
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectLymphoma, Large B-Cell, Diffuse
dc.subjectAntibodies, Monoclonal, Murine-Derived
dc.subjectRituximab
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.
dc.typeJournal Article
dcterms.dateAccepted2017-07-16
rioxxterms.funderThe Institute of Cancer Research
rioxxterms.identifier.projectUnspecified
rioxxterms.versionofrecord10.1093/annonc/mdx353
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2017-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfAnnals of oncology : official journal of the European Society for Medical Oncology
pubs.issue10
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine (RMH Smith Cunningham)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine (RMH Smith Cunningham)/Medicine (RMH Smith Cunningham) (hon.)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine (RMH Smith Cunningham)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine (RMH Smith Cunningham)/Medicine (RMH Smith Cunningham) (hon.)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume28
pubs.embargo.termsNo embargo
icr.researchteamMedicine (RMH Smith Cunningham)en_US
dc.contributor.icrauthorCunningham, Daviden
dc.contributor.icrauthorMarsden,en


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