Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33954
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dc.contributor.authorLewis, Katharine L-
dc.contributor.authorJakobsen, Lasse H-
dc.contributor.authorVilla, Diego-
dc.contributor.authorSmedby, Karin E-
dc.contributor.authorSavage, Kerry J-
dc.contributor.authorEyre, Toby A-
dc.contributor.authorCwynarski, Kate-
dc.contributor.authorBishton, Mark J-
dc.contributor.authorFox, Christopher P-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorMaurer, Matthew J-
dc.contributor.authorEl-Galaly, Tarec C-
dc.contributor.authorCheah, Chan Y-
dc.date2023-
dc.date.accessioned2023-10-11T06:21:17Z-
dc.date.available2023-10-11T06:21:17Z-
dc.date.issued2023-12-10-
dc.identifier.citationJournal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology 2023-12-10; 41(35)en_US
dc.identifier.issn1527-7755-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33954-
dc.description.abstractCNS progression or relapse is an uncommon but devastating complication of aggressive B-cell lymphoma. There is no consensus regarding the optimal approach to CNS prophylaxis. This study was designed to determine whether high-dose methotrexate (HD-MTX) is effective at preventing CNS progression in patients at high risk of this complication. Patients age 18-80 years with aggressive B-cell lymphoma and high risk of CNS progression, treated with curative-intent anti-CD20-based chemoimmunotherapy, were included in this international, retrospective, observational study. Cause-specific hazard ratios (HRs) and cumulative risks of CNS progression were calculated according to use of HD-MTX, with time to CNS progression calculated from diagnosis for all patients (all-pts) and from completion of frontline systemic lymphoma induction therapy, for patients in complete response at completion of chemoimmunotherapy (CR-pts). Two thousand four hundred eighteen all-pts (HD-MTX; n = 425) and 1,616 CR-pts (HD-MTX; n = 356) were included. CNS International Prognostic Index was 4-6 in 83.4% all-pts. Patients treated with HD-MTX had a lower risk of CNS progression (adjusted HR, 0.59 [95% CI, 0.38 to 0.90]; P = .014), but significance was not retained when confined to CR-pts (adjusted HR, 0.74 [95% CI, 0.42 to 1.30]; P = .29), with 5-year adjusted risk difference of 1.6% (95% CI, -1.5 to 4.4; all-pts) and 1.4% (95% CI, -1.5 to 4.1; CR-pts). Subgroups were underpowered to draw definitive conclusions regarding the efficacy of HD-MTX in individual high-risk clinical scenarios; however, there was no clear reduction in CNS progression risk with HD-MTX in any high-risk subgroup. In this large study, high-risk patients receiving HD-MTX had a 7.2% 2-year risk of CNS progression, consistent with the progression risk in previously reported high-risk cohorts. Use of HD-MTX was not associated with a clinically meaningful reduction in risk of CNS progression.en_US
dc.language.isoeng-
dc.titleHigh-Dose Methotrexate as CNS Prophylaxis in High-Risk Aggressive B-Cell Lymphoma.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Clinical Oncology : Official Journal of the American Society of Clinical Oncologyen_US
dc.identifier.affiliationLinear Clinical Research, Nedlands, WA, Australia.;Division of Haematology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia.;Division of Internal Medicine, Medical School, University of Western Australia, Perth, WA, Australia.en_US
dc.identifier.affiliationDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.en_US
dc.identifier.affiliationBC Cancer Centre for Lymphoid Cancer, The University of British Columbia, Vancouver, BC, Canada.en_US
dc.identifier.affiliationDepartment of Medicine Solna, Division of Clinical Epidemiology, Karolinska Institutet, Stockholm, Sweden.en_US
dc.identifier.affiliationBC Cancer Centre for Lymphoid Cancer, The University of British Columbia, Vancouver, BC, Canada.en_US
dc.identifier.affiliationOxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.en_US
dc.identifier.affiliationUniversity College London Hospital NHS Foundation Trust, London, United Kingdom.en_US
dc.identifier.affiliationUniversity of Nottingham, Nottingham, United Kingdom.en_US
dc.identifier.affiliationNottingham University Hospitals NHS Trust, Nottingham, United Kingdom.;University of Nottingham, Nottingham, United Kingdom.en_US
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen_US
dc.identifier.affiliationDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN.en_US
dc.identifier.affiliationDepartment of Haematology, Aalborg University Hospital, Aalborg, Denmark.en_US
dc.identifier.affiliationLinear Clinical Research, Nedlands, WA, Australia.;Division of Haematology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia.;Division of Internal Medicine, Medical School, University of Western Australia, Perth, WA, Australia.;Department of Haematology, PathWest, Nedlands, WA, Australia.en_US
dc.identifier.affiliationMonash University School of Public Health and Preventive Medicine, Melbourne, VIC, Australia.en_US
dc.identifier.doi10.1200/JCO.23.00365en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-0549-5877en_US
dc.identifier.orcid0000-0001-6575-7686en_US
dc.identifier.orcid0000-0002-4625-3009en_US
dc.identifier.orcid0000-0002-2104-3320en_US
dc.identifier.orcid0000-0002-5835-9863en_US
dc.identifier.orcid0000-0002-6631-9749en_US
dc.identifier.orcid0000-0001-6058-1036en_US
dc.identifier.orcid0000-0002-6322-9254en_US
dc.identifier.orcid0000-0002-0376-2559en_US
dc.identifier.orcid0000-0002-1867-0526en_US
dc.identifier.orcid0000-0001-7988-1565en_US
dc.identifier.pubmedid37797284-
dc.description.startpageJCO2300365-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
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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