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dc.contributor.authorHunter, Benjamin A
dc.contributor.authorEustace, A
dc.contributor.authorIrlam, Joely J
dc.contributor.authorValentine, Helen R
dc.contributor.authorDenley, H
dc.contributor.authorOguejiofor, Kenneth K
dc.contributor.authorSwindell, Ric
dc.contributor.authorHoskin, P
dc.contributor.authorChoudhury, Ananya
dc.contributor.authorWest, Catharine M L
dc.date.accessioned2014-07-08T14:29:16Z
dc.date.available2014-07-08T14:29:16Z
dc.date.issued2014-06-17
dc.identifier.citationExpression of hypoxia-inducible factor-1α predicts benefit from hypoxia modification in invasive bladder cancer. 2014: Br J Canceren
dc.identifier.issn1532-1827
dc.identifier.pmid24937673
dc.identifier.doi10.1038/bjc.2014.315
dc.identifier.urihttp://hdl.handle.net/10541/322591
dc.description.abstractBackground:The addition of carbogen and nicotinamide (CON) to radiotherapy (RT) improves overall survival in invasive bladder cancer. We explored whether expression of the hypoxia marker hypoxia-inducible factor-1α (HIF-1α) alone or in combination with other markers predicted benefit from CON.Methods:A retrospective study was carried out using material from patients with high-grade invasive bladder carcinoma enrolled in the BCON phase III trial of RT alone or with CON (RT+CON). HIF-1α expression was studied in 137 tumours using tissue microarrays and immunohistochemistry. Data were available from other studies for carbonic anhydrase IX and glucose transporter 1 protein and gene expression and tumour necrosis.Results:Patients with high HIF-1α expression had improved 5-year local relapse-free survival with RT+CON (47%) compared with RT alone (21%; hazard ratio (HR) 0.48, 95% CI 0.26-0.8, P=0.02), no benefit was seen with low HIF-1α expression (HR 0.81, 95% CI 0.43-1.50, P=0.5). Combinations of markers including necrosis also predicted benefit but did not improve on prediction using necrosis alone.Conclusions:HIF-1α may be used to predict benefit from CON in patients with bladder cancer but does not improve on use of necrosis.British Journal of Cancer advance online publication, 17 June 2014; doi:10.1038/bjc.2014.315 www.bjcancer.com.
dc.languageENG
dc.language.isoenen
dc.rightsArchived with thanks to British journal of canceren
dc.titleExpression of hypoxia-inducible factor-1α predicts benefit from hypoxia modification in invasive bladder cancer.en
dc.typeArticleen
dc.contributor.departmentTranslational Radiobiology Group, Institute of Cancer Sciences, University of Manchester, Manchester Academic Health Centre, Christie Hospital, Wilmslow Road, Manchester M20 4BX, UK.en
dc.identifier.journalBritish Journal of Canceren
html.description.abstractBackground:The addition of carbogen and nicotinamide (CON) to radiotherapy (RT) improves overall survival in invasive bladder cancer. We explored whether expression of the hypoxia marker hypoxia-inducible factor-1α (HIF-1α) alone or in combination with other markers predicted benefit from CON.Methods:A retrospective study was carried out using material from patients with high-grade invasive bladder carcinoma enrolled in the BCON phase III trial of RT alone or with CON (RT+CON). HIF-1α expression was studied in 137 tumours using tissue microarrays and immunohistochemistry. Data were available from other studies for carbonic anhydrase IX and glucose transporter 1 protein and gene expression and tumour necrosis.Results:Patients with high HIF-1α expression had improved 5-year local relapse-free survival with RT+CON (47%) compared with RT alone (21%; hazard ratio (HR) 0.48, 95% CI 0.26-0.8, P=0.02), no benefit was seen with low HIF-1α expression (HR 0.81, 95% CI 0.43-1.50, P=0.5). Combinations of markers including necrosis also predicted benefit but did not improve on prediction using necrosis alone.Conclusions:HIF-1α may be used to predict benefit from CON in patients with bladder cancer but does not improve on use of necrosis.British Journal of Cancer advance online publication, 17 June 2014; doi:10.1038/bjc.2014.315 www.bjcancer.com.


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