Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18363
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGleeson, Mary-
dc.contributor.authorPeckitt, Clare-
dc.contributor.authorCunningham, David-
dc.contributor.authorGibb, Adam-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorBack, Morgan-
dc.contributor.authorYasar, Binnaz-
dc.contributor.authorFoley, Kate-
dc.contributor.authorLee, Rebecca-
dc.contributor.authorDash, Joanna-
dc.contributor.authorJohnson, Hannah-
dc.contributor.authorO'Hara, Catherine-
dc.contributor.authorWotherspoon, Andrew-
dc.contributor.authorAttygalle, Ayoma-
dc.contributor.authorMenasce, Lia-
dc.contributor.authorShenjere, Patrick-
dc.contributor.authorPotter, Mike-
dc.contributor.authorEthell, Mark E-
dc.contributor.authorDearden, Claire-
dc.contributor.authorRadford, John-
dc.contributor.authorChau, Ian-
dc.contributor.authorLinton, Kim-
dc.date2017-11-09-
dc.date.accessioned2018-08-30T05:58:02Z-
dc.date.available2018-08-30T05:58:02Z-
dc.date.issued2018-07-
dc.identifier.citationLeukemia & lymphoma 2018; 59(7): 1586-1595-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18363-
dc.description.abstractWe evaluated the outcomes for patients with peripheral T-cell lymphoma (PTCL) undergoing front-line chemotherapy at our institutions between 2002 and 2012. One hundred and fifty-six patients were eligible, comprising PTCL not otherwise specified (NOS) (n = 50, 32.0%), angioimmunoblastic T-cell lymphoma (AITL) (n = 44, 28.2%), anaplastic large-cell lymphoma (ALCL) ALK negative (n = 23, 14.7%), ALCL ALK positive (n = 16, 10.3%), and other (n = 23, 14.7%). Most patients received CHOP (66.0%) and 13.0% received an autologous hematopoietic progenitor cell transplant (HPCT). With a median follow-up of 63.4 months, 5-year overall survival (OS) and progression-free survival (PFS) was 38.8% and 19.8% respectively. Independent risk factors for inferior OS were age >60 years, International Prognostic Index (IPI) ≥ 2 and lack of complete response to induction. When responding patients were compared by receipt of an autologous HPCT versus not, HPCT was associated with improved PFS (p = .001) and OS (p = .046) and remained significant for PFS in multivariate analysis suggesting a possible therapeutic benefit.-
dc.language.isoeng-
dc.subjectPeripheral T-cell lymphoma-
dc.subjectchemotherapy-
dc.subjecthematopoietic progenitor cell transplant-
dc.titleOutcomes following front-line chemotherapy in peripheral T-cell lymphoma: 10-year experience at The Royal Marsden and The Christie Hospital.-
dc.typeJournal Article-
dc.identifier.journaltitleLeukemia & lymphoma-
dc.identifier.affiliationThe Royal Marsden Hospital, London and Surrey , UKen
dc.identifier.affiliationDepartment of Oncology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationEastern Health, Melbourne, Australiaen
dc.identifier.affiliationThe University of Manchester and The Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UKen
dc.identifier.doi10.1080/10428194.2017.1393671-
dc.identifier.pubmedid29119842-
dc.type.austinJournal Article-
local.name.researcherHawkes, Eliza A
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

20
checked on Dec 22, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.