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 Field | Value | Language |
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dc.contributor.author | Lewis, Katharine L | - |
dc.contributor.author | Jakobsen, Lasse H | - |
dc.contributor.author | Villa, Diego | - |
dc.contributor.author | Smedby, Karin E | - |
dc.contributor.author | Savage, Kerry J | - |
dc.contributor.author | Eyre, Toby A | - |
dc.contributor.author | Cwynarski, Kate | - |
dc.contributor.author | Bishton, Mark J | - |
dc.contributor.author | Fox, Christopher P | - |
dc.contributor.author | Hawkes, Eliza A | - |
dc.contributor.author | Maurer, Matthew J | - |
dc.contributor.author | El-Galaly, Tarec C | - |
dc.contributor.author | Cheah, Chan Y | - |
dc.date | 2023 | - |
dc.date.accessioned | 2023-10-11T06:21:17Z | - |
dc.date.available | 2023-10-11T06:21:17Z | - |
dc.date.issued | 2023-12-10 | - |
dc.identifier.citation | Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology 2023-12-10; 41(35) | en_US |
dc.identifier.issn | 1527-7755 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/33954 | - |
dc.description.abstract | CNS 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.iso | eng | - |
dc.title | High-Dose Methotrexate as CNS Prophylaxis in High-Risk Aggressive B-Cell Lymphoma. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology | en_US |
dc.identifier.affiliation | Linear 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.affiliation | Department of Haematology, Aalborg University Hospital, Aalborg, Denmark. | en_US |
dc.identifier.affiliation | BC Cancer Centre for Lymphoid Cancer, The University of British Columbia, Vancouver, BC, Canada. | en_US |
dc.identifier.affiliation | Department of Medicine Solna, Division of Clinical Epidemiology, Karolinska Institutet, Stockholm, Sweden. | en_US |
dc.identifier.affiliation | BC Cancer Centre for Lymphoid Cancer, The University of British Columbia, Vancouver, BC, Canada. | en_US |
dc.identifier.affiliation | Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom. | en_US |
dc.identifier.affiliation | University College London Hospital NHS Foundation Trust, London, United Kingdom. | en_US |
dc.identifier.affiliation | University of Nottingham, Nottingham, United Kingdom. | en_US |
dc.identifier.affiliation | Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.;University of Nottingham, Nottingham, United Kingdom. | en_US |
dc.identifier.affiliation | Olivia Newton-John Cancer Wellness and Research Centre | en_US |
dc.identifier.affiliation | Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN. | en_US |
dc.identifier.affiliation | Department of Haematology, Aalborg University Hospital, Aalborg, Denmark. | en_US |
dc.identifier.affiliation | Linear 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.affiliation | Monash University School of Public Health and Preventive Medicine, Melbourne, VIC, Australia. | en_US |
dc.identifier.doi | 10.1200/JCO.23.00365 | en_US |
dc.type.content | Text | en_US |
dc.identifier.orcid | 0000-0003-0549-5877 | en_US |
dc.identifier.orcid | 0000-0001-6575-7686 | en_US |
dc.identifier.orcid | 0000-0002-4625-3009 | en_US |
dc.identifier.orcid | 0000-0002-2104-3320 | en_US |
dc.identifier.orcid | 0000-0002-5835-9863 | en_US |
dc.identifier.orcid | 0000-0002-6631-9749 | en_US |
dc.identifier.orcid | 0000-0001-6058-1036 | en_US |
dc.identifier.orcid | 0000-0002-6322-9254 | en_US |
dc.identifier.orcid | 0000-0002-0376-2559 | en_US |
dc.identifier.orcid | 0000-0002-1867-0526 | en_US |
dc.identifier.orcid | 0000-0001-7988-1565 | en_US |
dc.identifier.pubmedid | 37797284 | - |
dc.description.startpage | JCO2300365 | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
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 | - |
Appears in Collections: | Journal articles |
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