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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26807
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dc.contributor.authorEvens, Andrew M-
dc.contributor.authorConnors, Joseph M-
dc.contributor.authorYounes, Anas-
dc.contributor.authorAnsell, Stephen M-
dc.contributor.authorKim, Won Seog-
dc.contributor.authorRadford, John-
dc.contributor.authorFeldman, Tatyana-
dc.contributor.authorTuscano, Joseph-
dc.contributor.authorSavage, Kerry J-
dc.contributor.authorOki, Yasuhiro-
dc.contributor.authorGrigg, Andrew P-
dc.contributor.authorPocock, Christopher-
dc.contributor.authorDlugosz-Danecka, Monika-
dc.contributor.authorFenton, Keenan-
dc.contributor.authorForero-Torres, Andres-
dc.contributor.authorLiu, Rachael-
dc.contributor.authorJolin, Hina-
dc.contributor.authorGautam, Ashish-
dc.contributor.authorGallamini, Andrea-
dc.date2021-
dc.date.accessioned2021-06-28T06:12:07Z-
dc.date.available2021-06-28T06:12:07Z-
dc.date.issued2022-
dc.identifier.citationHaematologica 2022; 107(5): 1086-1094en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26807-
dc.description.abstractEffective and tolerable treatments are needed for older patients with classical Hodgkin lymphoma (cHL). We report results for older patients with cHL treated in the large phase III ECHELON-1 study of frontline brentuximab vedotin plus doxorubicin, vinblastine, and dacarbazine (A+AVD) versus doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD). Modified progression-free survival (PFS) per independent review facility (IRF) for older versus younger patients (aged ≥60 versus.en
dc.language.isoeng-
dc.subjectHodgkin lymphomaen
dc.subjectcanceren
dc.titleOlder patients (aged ≥60 years) with previously untreated advanced-stage classical Hodgkin lymphoma: a detailed analysis from the phase III ECHELON-1 study.en
dc.typeJournal Articleen
dc.identifier.journaltitleHaematologicaen
dc.identifier.affiliationDivision of Blood Disorders, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ..en
dc.identifier.affiliationBC Cancer Centre for Lymphoid Cancer and Department of Medical Oncology, Vancouver..en
dc.identifier.affiliationMemorial Sloan Kettering Cancer Center, NY..en
dc.identifier.affiliationMayo Clinic, Rochester, NY..en
dc.identifier.affiliationSungkyunkwan University School of Medicine, Samsung Medical Center, Seoul..en
dc.identifier.affiliationUniversity of Manchester and the Christie NHS Foundation Trust Manchester Academic Health Science Centre, Manchester..en
dc.identifier.affiliationJohn Theurer Cancer Center, NJ..en
dc.identifier.affiliationUC Davis Cancer Center, Sacramento, CA..en
dc.identifier.affiliationBC Cancer Centre for Lymphoid Cancer and Department of Medical Oncology, Vancouver..en
dc.identifier.affiliationGenentech, South San Francisco, CA..en
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen
dc.identifier.affiliationHaematology, East Kent Hospitals, Canterbury..en
dc.identifier.affiliationMaria Sklodowska-Curie National Research Institute of Oncology, Krakow..en
dc.identifier.affiliationSeagen Inc., Bothell, WA..en
dc.identifier.affiliationMillennium Pharmaceuticals, Inc., Cambridge, MA, USA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited..en
dc.identifier.affiliationResearch and Innovation Department, A Lacassagne Cancer Centre, Nice..en
dc.identifier.doi10.3324/haematol.2021.278438en
dc.type.contentTexten
dc.identifier.pubmedid34162178-
local.name.researcherGrigg, Andrew P
item.grantfulltextopen-
item.openairetypeJournal Article-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptClinical Haematology-
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