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dc.contributor.authorCorrie, PG
dc.contributor.authorMarshall, A
dc.contributor.authorNathan, PD
dc.contributor.authorLorigan, P
dc.contributor.authorGore, M
dc.contributor.authorTahir, S
dc.contributor.authorFaust, G
dc.contributor.authorKelly, CG
dc.contributor.authorMarples, M
dc.contributor.authorDanson, SJ
dc.contributor.authorMarshall, E
dc.contributor.authorHouston, SJ
dc.contributor.authorBoard, RE
dc.contributor.authorWaterston, AM
dc.contributor.authorNobes, JP
dc.contributor.authorHarries, M
dc.contributor.authorKumar, S
dc.contributor.authorGoodman, A
dc.contributor.authorDalgleish, A
dc.contributor.authorMartin-Clavijo, A
dc.contributor.authorWestwell, S
dc.contributor.authorCasasola, R
dc.contributor.authorChao, D
dc.contributor.authorMaraveyas, A
dc.contributor.authorPatel, PM
dc.contributor.authorOttensmeier, CH
dc.contributor.authorFarrugia, D
dc.contributor.authorHumphreys, A
dc.contributor.authorEccles, B
dc.contributor.authorYoung, G
dc.contributor.authorBarker, EO
dc.contributor.authorHarman, C
dc.contributor.authorWeiss, M
dc.contributor.authorMyers, KA
dc.contributor.authorChhabra, A
dc.contributor.authorRodwell, SH
dc.contributor.authorDunn, JA
dc.contributor.authorMiddleton, MR
dc.contributor.authorAVAST-M Investigators
dc.contributor.authorNathan, P
dc.contributor.authorLorigan, P
dc.contributor.authorDziewulski, P
dc.contributor.authorHolikova, S
dc.contributor.authorPanwar, U
dc.contributor.authorTahir, S
dc.contributor.authorFaust, G
dc.contributor.authorThomas, A
dc.contributor.authorCorrie, P
dc.contributor.authorSirohi, B
dc.contributor.authorKelly, C
dc.contributor.authorMiddleton, M
dc.contributor.authorMarples, M
dc.contributor.authorDanson, S
dc.contributor.authorLester, J
dc.contributor.authorMarshall, E
dc.contributor.authorAjaz, M
dc.contributor.authorHouston, S
dc.contributor.authorBoard, R
dc.contributor.authorEaton, D
dc.contributor.authorWaterston, A
dc.contributor.authorNobes, J
dc.contributor.authorLoo, S
dc.contributor.authorGray, G
dc.contributor.authorStubbings, H
dc.contributor.authorGore, M
dc.contributor.authorHarries, M
dc.contributor.authorKumar, S
dc.contributor.authorGoodman, A
dc.contributor.authorDalgleish, A
dc.contributor.authorMartin-Clavijo, A
dc.contributor.authorMarsden, J
dc.contributor.authorWestwell, S
dc.contributor.authorCasasola, R
dc.contributor.authorChao, D
dc.contributor.authorMaraveyas, A
dc.contributor.authorMarshall, E
dc.contributor.authorPatel, P
dc.contributor.authorOttensmeier, C
dc.contributor.authorFarrugia, D
dc.contributor.authorHumphreys, A
dc.contributor.authorEccles, B
dc.contributor.authorDega, R
dc.contributor.authorHerbert, C
dc.contributor.authorPrice, C
dc.contributor.authorBrunt, M
dc.contributor.authorScott-Brown, M
dc.contributor.authorHamilton, J
dc.contributor.authorHayward, RL
dc.contributor.authorSmyth, J
dc.contributor.authorWoodings, P
dc.contributor.authorNayak, N
dc.contributor.authorBurrows, L
dc.contributor.authorWolstenholme, V
dc.contributor.authorWagstaff, J
dc.contributor.authorNicolson, M
dc.contributor.authorWilson, A
dc.contributor.authorBarlow, C
dc.contributor.authorScrase, C
dc.contributor.authorPodd, T
dc.contributor.authorGonzalez, M
dc.contributor.authorStewart, J
dc.contributor.authorHighley, M
dc.contributor.authorWolstenholme, V
dc.contributor.authorGrumett, S
dc.contributor.authorGoodman, A
dc.contributor.authorTalbot, T
dc.contributor.authorNathan, K
dc.contributor.authorColtart, R
dc.contributor.authorGee, B
dc.contributor.authorGore, M
dc.contributor.authorFarrugia, D
dc.contributor.authorMartin-Clavijo, A
dc.contributor.authorMarsden, J
dc.contributor.authorPrice, C
dc.contributor.authorFarrugia, D
dc.contributor.authorNathan, K
dc.contributor.authorColtart, R
dc.contributor.authorNathan, K
dc.contributor.authorColtart, R
dc.date.accessioned2018-11-14T09:38:49Z
dc.date.issued2018-08
dc.identifier.citationAnnals of oncology : official journal of the European Society for Medical Oncology, 2018, 29 (8), pp. 1843 - 1852
dc.identifier.issn0923-7534
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2929
dc.identifier.eissn1569-8041
dc.identifier.doi10.1093/annonc/mdy229
dc.description.abstractBackground Bevacizumab is a recombinant humanised monoclonal antibody to vascular endothelial growth factor shown to improve survival in advanced solid cancers. We evaluated the role of adjuvant bevacizumab in melanoma patients at high risk of recurrence.Patients and methods Patients with resected AJCC stage IIB, IIC and III cutaneous melanoma were randomised to receive either adjuvant bevacizumab (7.5 mg/kg i.v. 3 weekly for 1 year) or standard observation. The primary end point was detection of an 8% difference in 5-year overall survival (OS) rate; secondary end points included disease-free interval (DFI) and distant metastasis-free interval (DMFI). Tumour and blood were analysed for prognostic and predictive markers.Results Patients (n=1343) recruited between 2007 and 2012 were predominantly stage III (73%), with median age 56 years (range 18-88 years). With 6.4-year median follow-up, 515 (38%) patients had died [254 (38%) bevacizumab; 261 (39%) observation]; 707 (53%) patients had disease recurrence [336 (50%) bevacizumab, 371 (55%) observation]. OS at 5 years was 64% for both groups [hazard ratio (HR) 0.98; 95% confidence interval (CI) 0.82-1.16, P = 0.78). At 5 years, 51% were disease free on bevacizumab versus 45% on observation (HR 0.85; 95% CI 0.74-0.99, P = 0.03), 58% were distant metastasis free on bevacizumab versus 54% on observation (HR 0.91; 95% CI 0.78-1.07, P = 0.25). Forty four percent of 682 melanomas assessed had a BRAFV600 mutation. In the observation arm, BRAF mutant patients had a trend towards poorer OS compared with BRAF wild-type patients (P = 0.06). BRAF mutation positivity trended towards better OS with bevacizumab (P = 0.21).Conclusions Adjuvant bevacizumab after resection of high-risk melanoma improves DFI, but not OS. BRAF mutation status may predict for poorer OS untreated and potential benefit from bevacizumab.Clinical trial information ISRCTN 81261306; EudraCT Number: 2006-005505-64.
dc.formatPrint
dc.format.extent1843 - 1852
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectAVAST-M Investigators
dc.subjectHumans
dc.subjectMelanoma
dc.subjectSkin Neoplasms
dc.subjectNeoplasm Recurrence, Local
dc.subjectProto-Oncogene Proteins B-raf
dc.subjectNeoplasm Staging
dc.subjectDisease-Free Survival
dc.subjectChemotherapy, Adjuvant
dc.subjectDrug Administration Schedule
dc.subjectSurvival Analysis
dc.subjectFollow-Up Studies
dc.subjectMutation
dc.subjectTime Factors
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.subjectWatchful Waiting
dc.subjectDermatologic Surgical Procedures
dc.subjectBevacizumab
dc.titleAdjuvant bevacizumab for melanoma patients at high risk of recurrence: survival analysis of the AVAST-M trial.
dc.typeJournal Article
rioxxterms.versionofrecord10.1093/annonc/mdy229
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfAnnals of oncology : official journal of the European Society for Medical Oncology
pubs.issue8
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume29
pubs.embargo.termsNot known
dc.contributor.icrauthorGore, Martinen


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