Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17423
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dc.contributor.authorKühnl, A-
dc.contributor.authorCunningham, D-
dc.contributor.authorCounsell, Nicholas-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorQian, W-
dc.contributor.authorSmith, P-
dc.contributor.authorChadwick, N-
dc.contributor.authorLawrie, A-
dc.contributor.authorMouncey, P-
dc.contributor.authorJack, A-
dc.contributor.authorPocock, C-
dc.contributor.authorArdeshna, Kirit M-
dc.contributor.authorRadford, J-
dc.contributor.authorMcMillan, A-
dc.contributor.authorDavies, J-
dc.contributor.authorTurner, D-
dc.contributor.authorKruger, A-
dc.contributor.authorJohnson, P W-
dc.contributor.authorGambell, J-
dc.contributor.authorRosenwald, A-
dc.contributor.authorOtt, G-
dc.contributor.authorHorn, H-
dc.contributor.authorZiepert, M-
dc.contributor.authorPfreundschuh, M-
dc.contributor.authorLinch, D-
dc.date.accessioned2018-04-12T01:50:38Z-
dc.date.available2018-04-12T01:50:38Z-
dc.date.issued2017-07-01-
dc.identifier.citationAnnals of oncology 2017; 28(7): 1540-1546-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17423-
dc.description.abstractThere is an on-going debate whether 2- or 3-weekly administration of R-CHOP is the preferred first-line treatment for elderly patients with diffuse large B-cell lymphoma (DLBCL). The UK NCRI R-CHOP14v21 randomized phase 3 trial did not demonstrate a difference in outcomes between R-CHOP-14 and R-CHOP-21 in newly diagnosed DLBCL patients aged 19-88 years, but data on elderly patients have not been reported in detail so far. Here, we provide a subgroup analysis of patients ≥60 years treated on the R-CHOP14v21 trial with extended follow-up. Six hundred and four R-CHOP14v21 patients ≥60 years were included in this subgroup analysis, with a median follow-up of 77.7 months. To assess the impact of MYC rearrangements (MYC-R) and double-hit-lymphoma (DHL) on outcome in elderly patients, we performed a joint analysis of cases with available molecular data from the R-CHOP14v21 (N = 217) and RICOVER-60 (N = 204) trials. Elderly DLBCL patients received high dose intensities with median total doses of ≥98% for all agents. Toxicities were similar in both arms with the exception of more grade ≥3 neutropenia (P < 0.0001) and fewer grade ≥3 thrombocytopenia (P = 0.05) in R-CHOP-21 versus R-CHOP-14. The elderly patient population had a favorable 5-year overall survival (OS) of 69% (95% CI: 65-73). We did not identify any subgroup of patients that showed differential response to either regimen. In multivariable analysis including individual factors of the IPI, gender, bulk, B2M and albumin levels, only age and B2M were of independent prognostic significance for OS. Molecular analyses demonstrated a significant impact of MYC-R (HR = 1.96; 95% CI: 1.22-3.16; P = 0.01) and DHL (HR = 2.21; 95% CI: 1.18-4.11; P = 0.01) on OS in the combined trial cohorts, independent of other prognostic factors. Our data support equivalence of both R-CHOP application forms in elderly DLBCL patients. Elderly MYC-R and DHL patients have inferior prognosis and should be considered for alternative treatment approaches. ISCRTN 16017947 (R-CHOP14v21); NCT00052936 (RICOVER-60).-
dc.language.isoeng-
dc.subjectMYC-
dc.subjectR-CHOP-
dc.subjectdiffuse large B-cell lymphoma-
dc.subjectdouble-hit lymphoma-
dc.subjectelderly-
dc.titleOutcome of elderly patients with diffuse large B-cell lymphoma treated with R-CHOP: results from the UK NCRI R-CHOP14v21 trial with combined analysis of molecular characteristics with the DSHNHL RICOVER-60 trial.-
dc.typeJournal Article-
dc.identifier.journaltitleAnnals of oncology : official journal of the European Society for Medical Oncology-
dc.identifier.affiliationDepartment of Medicine, The Royal Marsden NHS Foundation Trust, London and Surrey-
dc.identifier.affiliationCancer Research UK and UCL Cancer Trials Centre, UCL Cancer Institute, London, UK-
dc.identifier.affiliationOlivia-Newton John Cancer Research & Wellness Centre, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge-
dc.identifier.affiliationHMDS, St James's Institute of Oncology, Leeds-
dc.identifier.affiliationEast Kent Hospitals, Canterbury-
dc.identifier.affiliationDepartment of Hematology, University College London, London-
dc.identifier.affiliationMount Vernon Cancer Centre, Northwood-
dc.identifier.affiliationDepartment of Medical Oncology, University of Manchester and the Christie NHS Foundation Trust, Manchester-
dc.identifier.affiliationDepartment of Hematology, Nottingham City Hospital, Nottingham-
dc.identifier.affiliationWestern General Hospital, Edinburgh-
dc.identifier.affiliationDepartment of Hematology, Torbay Hospital, Torquay-
dc.identifier.affiliationRoyal Cornwall Hospital, Truro-
dc.identifier.affiliationCancer Research UK Center, University of Southampton, Southampton, UK-
dc.identifier.affiliationInstitute of Pathology, Würzburg University, Würzburg-
dc.identifier.affiliationDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart-
dc.identifier.affiliationDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart and University of Tübingen, Stuttgart-
dc.identifier.affiliationInstitute for Medical Informatics, Statistics, and Epidemiology, University of Leipzig, Leipzig-
dc.identifier.affiliationDepartment of Medicine, Saarland University Medical School, Homburg/Saar, Germany-
dc.identifier.doi10.1093/annonc/mdx128-
dc.identifier.pubmedid28398499-
dc.type.austinClinical Trial, Phase III-
dc.type.austinComparative Study-
dc.type.austinJournal Article-
dc.type.austinRandomized Controlled Trial-
local.name.researcherHawkes, Eliza A
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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