Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27295
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dc.contributor.authorSiu, Ho Wai Derrick-
dc.contributor.authorTebbutt, Niall C-
dc.contributor.authorChantrill, Lorraine-
dc.contributor.authorKarapetis, Chris-
dc.contributor.authorSteer, Christopher-
dc.contributor.authorWilson, Kate-
dc.contributor.authorEspinoza, David-
dc.contributor.authorBailey, Lisa-
dc.contributor.authorYip, Sonia-
dc.contributor.authorCuff, Jeff-
dc.contributor.authorPavlakis, Nick-
dc.contributor.authorThavaneswaran, Subotheni-
dc.contributor.authorBriscoe, Karen-
dc.contributor.authorSrivastav, Ratnesh-
dc.contributor.authorShannon, Jennifer-
dc.contributor.authorSegelov, Eva-
dc.contributor.authorTie, Jeannie-
dc.contributor.authorCaird, Susan-
dc.contributor.authorFrancesconi, Alessandra-
dc.contributor.authorPrice, Timothy-
dc.contributor.authorWuttke, Melanie-
dc.contributor.authorLadwa, Rahul-
dc.contributor.authorSjoquist, Katrin-
dc.contributor.authorBurge, Matthew-
dc.date2021-08-18-
dc.date.accessioned2021-08-23T05:59:00Z-
dc.date.available2021-08-23T05:59:00Z-
dc.date.issued2021-08-18-
dc.identifier.citationBMC Cancer 2021; 21(1): 932en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27295-
dc.description.abstractDoublet chemotherapy in combination with a biologic agent has been a standard of care in patients with metastatic colorectal cancer for over a decade. The evidence for a "lighter" treatment approach is limited to mono-chemotherapy plus bevacizumab in the RAS unselected population. Anti-EGFR antibodies have activity as monotherapy or in combination with chemotherapy in RAS wildtype metastatic colorectal cancer; however their role in first-line treatment in combination with 5-fluorouracil monotherapy or when given alone has not been well studied. MONARCC aims to investigate this approach in an elderly population. MONARCC is a prospective, open-label, multicentre, non-comparative randomised phase II trial. Eligible patients aged ≥70 with unresectable metastatic, untreated, RAS/BRAF wildtype metastatic colorectal cancer will be randomised 1:1 to receive panitumumab alone or panitumumab plus infusional 5-fluorouracil. RAS and BRAF analyses will be performed in local laboratories. Comprehensive Health Assessment and Limited Health Assessments will be performed at baseline and at 16 weeks, respectively, to assess frailty. The Patient Symptom Questionnaire and Overall Treatment Utility are to be undertaken at different timepoints to assess the impact of treatment-related toxicities and quality of life. Treatment will be delivered every 2 weeks until disease progression, unacceptable toxicity (as determined by treating clinician or patient), delay of treatment of more than 6 weeks, or withdrawal of consent. The primary end point is 6-month progression-free survival in both arms. Secondary end points include overall survival, time to treatment failure, objective tumour response rate as defined by RECIST v1.1 and safety (adverse events). Tertiary and correlative endpoints include the feasibility and utility of a comprehensive geriatric assessment, quality of life and biological substudies. MONARCC investigates the activity and tolerability of first-line panitumumab-based treatments with a view to expand on current treatment options while maximising progression-free and overall survival and quality of life in molecularly selected elderly patients with metastatic colorectal cancer. Australia New Zealand Clinical Trials Registry: ACTRN12618000233224 , prospectively registered 14 February 2018.en
dc.language.isoeng-
dc.subjectBRAFen
dc.subjectCetuximaben
dc.subjectClinical trialen
dc.subjectElderlyen
dc.subjectMetastatic colorectal canceren
dc.subjectOlder adultsen
dc.subjectPanitumumaben
dc.subjectRASen
dc.titleMONARCC: a randomised phase II study of panitumumab monotherapy and panitumumab plus 5-fluorouracil as first-line therapy for RAS and BRAF wildtype metastatic colorectal cancer: a study by the Australasian Gastrointestinal Trials Group (AGITG).en
dc.typeJournal Articleen
dc.identifier.journaltitleBMC Canceren
dc.identifier.affiliationThe Prince Charles Hospital, Brisbane, Australiaen
dc.identifier.affiliationRoyal Hobart Hospital, Hobart, Australiaen
dc.identifier.affiliationPrincess Alexandra Hospital, Brisbane, Australiaen
dc.identifier.affiliationRoyal Brisbane and Women's Hospital, Brisbane, Australiaen
dc.identifier.affiliationNHMRC Clinical Trials Centre, University of Sydney, Sydney, Australiaen
dc.identifier.affiliation, Camperdown, Australiaen
dc.identifier.affiliationAustin Healthen
dc.identifier.affiliationShoalhaven Cancer Care Centre, Nowra, Australiaen
dc.identifier.affiliationFlinders Medical Centre, Adelaide, Australiaen
dc.identifier.affiliationBorder Medical Oncology Research Unit, Albury-Wodonga, Australiaen
dc.identifier.affiliationAustralasian Gastrointestinal Group (AGITG), Sydney, Australiaen
dc.identifier.affiliationNorthern Cancer Institute, Sydney, Australiaen
dc.identifier.affiliationSt Vincent's Public Hospital, Sydney, Australiaen
dc.identifier.affiliationCoffs Harbour Health Campus, Coffs Harbour, Australiaen
dc.identifier.affiliationThe Tweed Hospital, Tweed Heads, Australiaen
dc.identifier.affiliationNepean Hospital, Sydney, Australiaen
dc.identifier.affiliationMonash Medical Centre, Melbourne, Australiaen
dc.identifier.affiliationSunshine Hospital, Melbourne, Australiaen
dc.identifier.affiliationGold Coast University Hospital, Gold Coast, Australiaen
dc.identifier.affiliationSunshine Coast University Hospital, Sunshine Coast, Australiaen
dc.identifier.affiliationThe Queen Elizabeth Hospital, Adelaide, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen
dc.identifier.doi10.1186/s12885-021-08644-4en
dc.type.contentTexten
dc.identifier.orcid0000-0002-2219-2459en
dc.identifier.pubmedid34407800-
local.name.researcherTebbutt, Niall C
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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