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dc.contributor.authorCrabb, SJ
dc.contributor.authorMartin, K
dc.contributor.authorAbab, J
dc.contributor.authorRatcliffe, I
dc.contributor.authorThornton, R
dc.contributor.authorLineton, B
dc.contributor.authorEllis, M
dc.contributor.authorMoody, R
dc.contributor.authorStanton, L
dc.contributor.authorGalanopoulou, A
dc.contributor.authorMaishman, T
dc.contributor.authorGeldart, T
dc.contributor.authorBayne, M
dc.contributor.authorDavies, J
dc.contributor.authorLamb, C
dc.contributor.authorPopat, S
dc.contributor.authorJoffe, JK
dc.contributor.authorNutting, C
dc.contributor.authorChester, J
dc.contributor.authorHartley, A
dc.contributor.authorThomas, G
dc.contributor.authorOttensmeier, C
dc.contributor.authorHuddart, R
dc.contributor.authorKing, E
dc.date.accessioned2017-11-22T10:27:39Z
dc.date.issued2017-12-01
dc.identifier.citationEuropean journal of cancer (Oxford, England : 1990), 2017, 87 pp. 75 - 83
dc.identifier.issn0959-8049
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/918
dc.identifier.eissn1879-0852
dc.identifier.doi10.1016/j.ejca.2017.09.033
dc.description.abstractBACKGROUND: Cisplatin is one of the most ototoxic chemotherapy drugs, resulting in a permanent and irreversible hearing loss in up to 50% of patients. Cisplatin and gentamicin are thought to damage hearing through a common mechanism, involving reactive oxygen species in the inner ear. Aspirin has been shown to minimise gentamicin-induced ototoxicity. We, therefore, tested the hypothesis that aspirin could also reduce ototoxicity from cisplatin-based chemotherapy. METHODS: A total of 94 patients receiving cisplatin-based chemotherapy for multiple cancer types were recruited into a phase II, double-blind, placebo-controlled trial and randomised in a ratio of 1:1 to receive aspirin 975 mg tid and omeprazole 20 mg od, or matched placebos from the day before, to 2 days after, their cisplatin dose(s), for each treatment cycle. Patients underwent pure tone audiometry before and at 7 and 90 days after their final cisplatin dose. The primary end-point was combined hearing loss (cHL), the summed hearing loss at 6 kHz and 8 kHz, in both ears. RESULTS: Although aspirin was well tolerated, it did not protect hearing in patients receiving cisplatin (p-value = 0.233, 20% one-sided level of significance). In the aspirin arm, patients demonstrated mean cHL of 49 dB (standard deviation [SD] 61.41) following cisplatin compared with placebo patients who demonstrated mean cHL of 36 dB (SD 50.85). Women had greater average hearing loss than men, and patients treated for head and neck malignancy experienced the greatest cHL. CONCLUSIONS: Aspirin did not protect from cisplatin-related ototoxicity. Cisplatin and gentamicin may therefore have distinct ototoxic mechanisms, or cisplatin-induced ototoxicity may be refractory to the aspirin regimen used here.
dc.formatPrint-Electronic
dc.format.extent75 - 83
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectHearing Loss
dc.subjectCisplatin
dc.subjectAspirin
dc.subjectAntineoplastic Agents
dc.subjectProtective Agents
dc.subjectAudiometry, Pure-Tone
dc.subjectTreatment Outcome
dc.subjectDrug Administration Schedule
dc.subjectDouble-Blind Method
dc.subjectHearing
dc.subjectCytoprotection
dc.subjectTime Factors
dc.subjectAdult
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.subjectUnited Kingdom
dc.titleCOAST (Cisplatin ototoxicity attenuated by aspirin trial): A phase II double-blind, randomised controlled trial to establish if aspirin reduces cisplatin induced hearing-loss.
dc.typeJournal Article
dcterms.dateAccepted2017-09-25
rioxxterms.versionofrecord10.1016/j.ejca.2017.09.033
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.licenseref.startdate2017-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean journal of cancer (Oxford, England : 1990)
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
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/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume87
pubs.embargo.termsNo embargo
icr.researchteamThoracic Oncology
icr.researchteamClinical Academic Radiotherapy (Huddart)
dc.contributor.icrauthorHuddart, Robert


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