Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/41873
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dc.contributor.authorMitchell P.L.R.en
dc.contributor.authorQuinn M.A.en
dc.contributor.authorJobling T.W.en
dc.contributor.authorLoveland B.E.en
dc.contributor.authorGargosky S.E.en
dc.contributor.authorMcKenzie I.F.C.en
dc.contributor.authorPietersz G.en
dc.contributor.authorVaughan H.en
dc.contributor.authorKaranikas V.en
dc.contributor.authorZhao A.en
dc.contributor.authorWhite S.C.en
dc.contributor.authorAllen D.G.en
dc.contributor.authorGrant P.T.en
dc.date.accessioned2021-05-14T14:21:42Zen
dc.date.available2021-05-14T14:21:42Zen
dc.date.copyright2014en
dc.date.created20150423en
dc.date.issued2015-04-23en
dc.identifier.citationJournal for ImmunoTherapy of Cancer. 2 (1) (no pagination), 2014. Article Number: 16. Date of Publication: June 18, 2014.en
dc.identifier.issn2051-1426 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/41873en
dc.description.abstractBackground: Mucin 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. Method(s): 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. Result(s): 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). Conclusion(s): 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.Copyright © 2014 Mitchell et al.; licensee BioMed Central Ltd.en
dc.languageenen
dc.languageEnglishen
dc.publisherBioMed Central Ltd. (E-mail: info@biomedcentral.com)en
dc.relation.ispartofJournal for ImmunoTherapy of 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.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1186/2051-1426-2-16en
dc.publisher.placeUnited Kingdomen
dc.identifier.source603837259en
dc.identifier.institution(Mitchell, White) Medical Oncology Unit, Austin Hospital, Olivia Newton-John Cancer and Wellness Centre, 145 Studley Road, Heidelberg, VIC 3084, Australia (Quinn) Royal Womens Hospital, 20 Flemington Road, Parkville, VIC 3052, Australia (Grant, Allen) Mercy Hospital for Women, 163 Studley Road, Heidelberg, VIC 3084, Australia (Jobling) Monash Medical Centre, Clayton Road, Clayton, VIC 3168, Australia (Zhao, Karanikas, Vaughan, Pietersz, McKenzie, Loveland) Burnet Institute, 85 Commercial Road, Melbourne, VIC 3004, Australia (Jobling, Loveland) Monash University, Wellington Road, Clayton, VIC 3168, Australia (Gargosky) Prima BioMed Ltd., 151 Macquarie Street, Sydney, NSW 2001, Australia (Mitchell, Quinn, Grant, Allen, Pietersz) University of Melbourne, Parkville, VIC 3052, Australia (Karanikas) Roche Innovation Center Zurich, Schlieren 8952, Switzerlanden
dc.description.addressP.L.R. Mitchell, Medical Oncology Unit, Austin Hospital, Olivia Newton-John Cancer and Wellness Centre, 145 Studley Road, Heidelberg, VIC 3084, Australiaen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2015 Elsevier B.V., All rights reserved.en
dc.subect.keywordsCA125 Immunotherapy Ovarian canceren
dc.identifier.authoremailWhite S.C.; shane.white@nh.org.au Zhao A.; ayzhao@burnet.edu.au Vaughan H.; quinkin1@optusnet.com.au McKenzie I.F.C.; ifcmckenzie@gmail.com Jobling T.W.; tjobling@bigpond.net.au Loveland B.E.; bloveland@burnet.edu.au Gargosky S.E.; sharron.gargosky@primabiomed.com.au Mitchell P.L.R.; Paul.MITCHELL@austin.org.au Quinn M.A.; maquinn@unimelb.edu.au Grant P.T.; PGrant@mercy.com.au Allen D.G.; DAllen@mercy.com.au Pietersz G.; gpietersz@burnet.edu.au Karanikas V.; vaios.karanikas@roche.comen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptObstetrics and Gynaecology (Monash Women's)-
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