Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/24459
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Straus, David | - |
dc.contributor.author | Collins, Graham | - |
dc.contributor.author | Walewski, Jan | - |
dc.contributor.author | Zinzani, Pier Luigi | - |
dc.contributor.author | Grigg, Andrew P | - |
dc.contributor.author | Sureda, Anna | - |
dc.contributor.author | Illes, Arpad | - |
dc.contributor.author | Kim, Tae Min | - |
dc.contributor.author | Alekseev, Sergey | - |
dc.contributor.author | Specht, Lena | - |
dc.contributor.author | Buccheri, Valeria | - |
dc.contributor.author | Younes, Anas | - |
dc.contributor.author | Connors, Joseph | - |
dc.contributor.author | Forero-Torres, Andres | - |
dc.contributor.author | Fenton, Keenan | - |
dc.contributor.author | Gautam, Ashish | - |
dc.contributor.author | Purevjal, Indra | - |
dc.contributor.author | Liu, Rachael | - |
dc.contributor.author | Gallamini, Andrea | - |
dc.date | 2020-08-25 | - |
dc.date.accessioned | 2020-09-28T20:40:03Z | - |
dc.date.available | 2020-09-28T20:40:03Z | - |
dc.date.issued | 2020-12-25 | - |
dc.identifier.citation | Leukemia & Lymphoma 2020; 61(12): 2931-2938 | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/24459 | - |
dc.description.abstract | We 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.iso | eng | - |
dc.subject | Hodgkin lymphoma | en |
dc.subject | brentuximab vedotin | en |
dc.subject | frontline therapy | en |
dc.subject | growth factor | en |
dc.subject | primary prophylaxis | en |
dc.title | Primary 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.type | Journal Article | en |
dc.identifier.journaltitle | Leukemia & Lymphoma | en |
dc.identifier.affiliation | Memorial Sloan Kettering Cancer Center, New York City, NY, USA | en |
dc.identifier.affiliation | Clinical Haematology | en |
dc.identifier.affiliation | Oxford Cancer and Hematology Center, Churchill Hospital, Oxford, UK | en |
dc.identifier.affiliation | BC Cancer Centre for Lymphoid Cancer, Vancouver, Canada | en |
dc.identifier.affiliation | Maria Sklodowska-Curie Memorial Institute and Oncology Center, Warsaw, Poland | en |
dc.identifier.affiliation | Institute of Hematology Seragnoli, University of Bologna, Bologna, Italy | en |
dc.identifier.affiliation | Institut Català d'Oncologia-Hospitalet, Hospital Quirón Dexeus, Barcelona, Spain | en |
dc.identifier.affiliation | University of Debrecen, Faculty of Medicine, Debrecen, Hungary | en |
dc.identifier.affiliation | Seoul National University Hospital, Seoul, Republic of Korea | en |
dc.identifier.affiliation | Petrov Research Institute of Oncology, St. Petersburg, Russia | en |
dc.identifier.affiliation | Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark | en |
dc.identifier.affiliation | Hematology Service, Hospital das Clinicas HCFMUSP, Faculty of Medicine, University of São Paulo, São Paulo, Brazil | en |
dc.identifier.affiliation | Memorial Sloan Kettering Cancer Center, New York City, NY, USA | en |
dc.identifier.affiliation | Seattle Genetics, Bothell, WA, USA | en |
dc.identifier.affiliation | Millennium Pharmaceuticals, Cambridge, MA, USA | en |
dc.identifier.affiliation | Research and Clinical Innovation, Antoine-Lacassagne Cancer Center, Nice, France | en |
dc.identifier.doi | 10.1080/10428194.2020.1791846 | en |
dc.type.content | Text | en |
dc.identifier.orcid | 0000-0001-6033-4510 | en |
dc.identifier.pubmedid | 32842815 | - |
local.name.researcher | Grigg, Andrew P | |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
crisitem.author.dept | Clinical Haematology | - |
Appears in Collections: | Journal articles |
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