Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12291
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMitchell, Paul L Ren
dc.contributor.authorQuinn, Michael Aen
dc.contributor.authorGrant, Peteren
dc.contributor.authorAllen, David Gen
dc.contributor.authorJobling, Thomas Wen
dc.contributor.authorWhite, Shane Cen
dc.contributor.authorZhao, Anneen
dc.contributor.authorKaranikas, Vaiosen
dc.contributor.authorVaughan, Hilary Aen
dc.contributor.authorPietersz, Geoffrey Aen
dc.contributor.authorMcKenzie, Ian F Cen
dc.contributor.authorGargosky, Sharron Een
dc.contributor.authorLoveland, Bruce Een
dc.date.accessioned2015-05-16T01:57:14Z-
dc.date.available2015-05-16T01:57:14Z-
dc.date.issued2014-06-18en
dc.identifier.citationJournal For Immunotherapy of Cancer 2014; 2: 16en
dc.identifier.govdoc24995129en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12291en
dc.description.abstractMucin 1 antigen, highly expressed by epithelial ovarian cancer (EOC), is a potential target for immunotherapy. A previous successful phase 1 trial was conducted in patients with adenocarcinoma who were injected with Cvac, autologous monocyte-derived dendritic cells (DCs) incubated with mannosylated mucin 1 protein (M-FP). The present study was a phase 2 trial of Cvac in patients with advanced EOC.Eligible patients had EOC with progressive disease, defined as an increase in CA125 of ≥ 25% in 1 month. The primary endpoint was CA125 response or stabilization. Peripheral blood mononuclear cells were collected by leukapheresis and cultured to generate DCs. The DC were incubated with M-FP, and after washing were prepared for injection into the patient intradermally every 4 weeks for 3 doses, then every 10 weeks for up to 12 months.All 28 patients recruited were evaluable for safety and 26 for efficacy. All had undergone surgery and platinum-based chemotherapy, and 57% of patients received ≥ 3 chemotherapy regimens. There were no Grade 3 or 4 toxicities considered related to Cvac. Four patients showed CA125 response or stabilization (2 patients with major responses, 1 minor response, 1 stabilization) of median duration 10.3 months (5.3-16.3 months). An additional patient had > 25% CA125 reduction (not confirmed).Cvac immunotherapy was well tolerated. Clinical activity in EOC was evident based on decline or stabilization of CA125 in some patients, supporting ongoing development of Cvac in ovarian carcinoma and planning of additional trials of patients in remission is currently underway.en
dc.language.isoenen
dc.subject.otherCA125en
dc.subject.otherImmunotherapyen
dc.subject.otherOvarian canceren
dc.titleA phase 2, single-arm study of an autologous dendritic cell treatment against mucin 1 in patients with advanced epithelial ovarian cancer.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal for immunotherapy of canceren
dc.identifier.affiliationMonash Medical Centre, Clayton Road, Clayton, VIC 3168, Australiaen
dc.identifier.affiliationMercy Hospital for Women, 163 Studley Road, Heidelberg, VIC 3084, Australiaen
dc.identifier.affiliationUniversity of Melbourne, Parkville, VIC 3052, Australiaen
dc.identifier.affiliationBurnet Institute, 85 Commercial Road, Melbourne, VIC 3004, Australiaen
dc.identifier.affiliationMonash University, Wellington Road, Clayton, VIC 3168, Australiaen
dc.identifier.affiliationPrima BioMed, Ltd., 151 Macquarie Street, Sydney, NSW 2001, Australiaen
dc.identifier.affiliationRoyal Womens Hospital, 20 Flemington Road, Parkville, VIC 3052, Australiaen
dc.identifier.affiliationUniversity of Melbourne, Parkville, VIC 3052, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationRoche Innovation Center Zurich, 8952 Schlieren, Switzerlanden
dc.identifier.affiliationDepartment of Medical Oncology, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1186/2051-1426-2-16en
dc.description.pages16en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24995129en
dc.type.austinJournal Articleen
local.name.researcherMitchell, Paul L R
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.openairetypeJournal Article-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
Appears in Collections:Journal articles
Files in This Item:
File Description SizeFormat 
24995129.pdf475.75 kBAdobe PDFThumbnail
View/Open
Show simple item record

Page view(s)

28
checked on Dec 27, 2024

Download(s)

84
checked on Dec 27, 2024

Google ScholarTM

Check


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