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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. | Austin Authors: | Straus, David;Collins, Graham;Walewski, Jan;Zinzani, Pier Luigi;Grigg, Andrew P ;Sureda, Anna;Illes, Arpad;Kim, Tae Min;Alekseev, Sergey;Specht, Lena;Buccheri, Valeria;Younes, Anas;Connors, Joseph;Forero-Torres, Andres;Fenton, Keenan;Gautam, Ashish;Purevjal, Indra;Liu, Rachael;Gallamini, Andrea | Affiliation: | Memorial Sloan Kettering Cancer Center, New York City, NY, USA Clinical Haematology Oxford Cancer and Hematology Center, Churchill Hospital, Oxford, UK BC Cancer Centre for Lymphoid Cancer, Vancouver, Canada Maria Sklodowska-Curie Memorial Institute and Oncology Center, Warsaw, Poland Institute of Hematology Seragnoli, University of Bologna, Bologna, Italy Institut Català d'Oncologia-Hospitalet, Hospital Quirón Dexeus, Barcelona, Spain University of Debrecen, Faculty of Medicine, Debrecen, Hungary Seoul National University Hospital, Seoul, Republic of Korea Petrov Research Institute of Oncology, St. Petersburg, Russia Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Hematology Service, Hospital das Clinicas HCFMUSP, Faculty of Medicine, University of São Paulo, São Paulo, Brazil Memorial Sloan Kettering Cancer Center, New York City, NY, USA Seattle Genetics, Bothell, WA, USA Millennium Pharmaceuticals, Cambridge, MA, USA Research and Clinical Innovation, Antoine-Lacassagne Cancer Center, Nice, France |
Issue Date: | 25-Dec-2020 | Date: | 2020-08-25 | Publication information: | Leukemia & Lymphoma 2020; 61(12): 2931-2938 | 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. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/24459 | DOI: | 10.1080/10428194.2020.1791846 | ORCID: | 0000-0001-6033-4510 | Journal: | Leukemia & Lymphoma | PubMed URL: | 32842815 | Type: | Journal Article | Subjects: | Hodgkin lymphoma brentuximab vedotin frontline therapy growth factor primary prophylaxis |
Appears in Collections: | Journal articles |
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