Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24459
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dc.contributor.authorStraus, David-
dc.contributor.authorCollins, Graham-
dc.contributor.authorWalewski, Jan-
dc.contributor.authorZinzani, Pier Luigi-
dc.contributor.authorGrigg, Andrew P-
dc.contributor.authorSureda, Anna-
dc.contributor.authorIlles, Arpad-
dc.contributor.authorKim, Tae Min-
dc.contributor.authorAlekseev, Sergey-
dc.contributor.authorSpecht, Lena-
dc.contributor.authorBuccheri, Valeria-
dc.contributor.authorYounes, Anas-
dc.contributor.authorConnors, Joseph-
dc.contributor.authorForero-Torres, Andres-
dc.contributor.authorFenton, Keenan-
dc.contributor.authorGautam, Ashish-
dc.contributor.authorPurevjal, Indra-
dc.contributor.authorLiu, Rachael-
dc.contributor.authorGallamini, Andrea-
dc.date2020-08-25-
dc.date.accessioned2020-09-28T20:40:03Z-
dc.date.available2020-09-28T20:40:03Z-
dc.date.issued2020-12-25-
dc.identifier.citationLeukemia & Lymphoma 2020; 61(12): 2931-2938en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/24459-
dc.description.abstractWe investigate the impact of granulocyte-colony stimulating factor (G-CSF) primary prophylaxis (G-PP, N = 83) versus no G-PP (N = 579) on safety and efficacy of brentuximab vedotin plus doxorubicin, vinblastine, and dacarbazine (A + AVD) in the ECHELON-1 study of previously untreated stage III/IV classical Hodgkin lymphoma. G-PP was associated with lower incidence of ≥ grade 3 neutropenia (29% versus 70%) and febrile neutropenia (11% versus 21%). Fewer dose delays (35% versus 49%), reductions (20% versus 26%), and hospitalizations (29% versus 38%) were observed. Seven neutropenia-associated deaths occurred in the A + AVD arm; none received G-PP. A + AVD with G-PP was associated with decreased risk of a modified progression-free survival event by 26% compared with A + AVD alone (95% CI: 0.40-1.37). G-PP reduced the rate and severity of adverse events, including febrile neutropenia, reduced treatment delays, dose reductions, and discontinuations, and may thus improve efficacy outcomes. These data support G-PP for all patients treated with A + AVD.en
dc.language.isoeng-
dc.subjectHodgkin lymphomaen
dc.subjectbrentuximab vedotinen
dc.subjectfrontline therapyen
dc.subjectgrowth factoren
dc.subjectprimary prophylaxisen
dc.titlePrimary prophylaxis with G-CSF may improve outcomes in patients with newly diagnosed stage III/IV Hodgkin lymphoma treated with brentuximab vedotin plus chemotherapy.en
dc.typeJournal Articleen
dc.identifier.journaltitleLeukemia & Lymphomaen
dc.identifier.affiliationMemorial Sloan Kettering Cancer Center, New York City, NY, USAen
dc.identifier.affiliationClinical Haematologyen
dc.identifier.affiliationOxford Cancer and Hematology Center, Churchill Hospital, Oxford, UKen
dc.identifier.affiliationBC Cancer Centre for Lymphoid Cancer, Vancouver, Canadaen
dc.identifier.affiliationMaria Sklodowska-Curie Memorial Institute and Oncology Center, Warsaw, Polanden
dc.identifier.affiliationInstitute of Hematology Seragnoli, University of Bologna, Bologna, Italyen
dc.identifier.affiliationInstitut Català d'Oncologia-Hospitalet, Hospital Quirón Dexeus, Barcelona, Spainen
dc.identifier.affiliationUniversity of Debrecen, Faculty of Medicine, Debrecen, Hungaryen
dc.identifier.affiliationSeoul National University Hospital, Seoul, Republic of Koreaen
dc.identifier.affiliationPetrov Research Institute of Oncology, St. Petersburg, Russiaen
dc.identifier.affiliationDepartment of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmarken
dc.identifier.affiliationHematology Service, Hospital das Clinicas HCFMUSP, Faculty of Medicine, University of São Paulo, São Paulo, Brazilen
dc.identifier.affiliationMemorial Sloan Kettering Cancer Center, New York City, NY, USAen
dc.identifier.affiliationSeattle Genetics, Bothell, WA, USAen
dc.identifier.affiliationMillennium Pharmaceuticals, Cambridge, MA, USAen
dc.identifier.affiliationResearch and Clinical Innovation, Antoine-Lacassagne Cancer Center, Nice, Franceen
dc.identifier.doi10.1080/10428194.2020.1791846en
dc.type.contentTexten
dc.identifier.orcid0000-0001-6033-4510en
dc.identifier.pubmedid32842815-
local.name.researcherGrigg, Andrew P
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptClinical Haematology-
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