Show simple item record

dc.contributor.authorPalmer, DHen
dc.contributor.authorHussain, SAen
dc.contributor.authorSmith, AJen
dc.contributor.authorHargreaves, Sen
dc.contributor.authorMa, YTen
dc.contributor.authorHull, Den
dc.contributor.authorJohnson, PJen
dc.contributor.authorRoss, PJen
dc.date.accessioned2018-01-22T11:18:56Z
dc.date.available2018-01-22T11:18:56Z
dc.date.issued2013-08-20en
dc.identifier.urihttp://hdl.handle.net/10026.1/10637
dc.description.abstract

BACKGROUND: The prognosis for hepatocellular carcinoma (HCC) is dependent upon tumour stage, performance status (PS), severity of underlying liver disease, and the availability of appropriate therapies. The unavailability of sorafenib may have a significantly adverse effect on the prognosis of UK patients with advanced HCC. During the study period, access to sorafenib was at the discretion of local health funding bodies, a process that may delay or deny access to the drug and that remains in place for Wales, Scotland, and Northern Ireland. Here, we attempt to address the impact of this system on patients with advanced HCC in the United Kingdom. METHODS: This is a retrospective study performed in the two largest specialist hepatobiliary oncology units in the United Kingdom. Funding applications were made to local funding bodies for patients with advanced HCC for whom sorafenib was considered appropriate (advanced HCC not suitable for loco-regional therapies, compensated chronic liver disease, PS 0-2). RESULTS: A total of 133 applications were made, of which 57 (43%) were approved and 76 (57%) declined. Demographics and prognostic factors were balanced between the two groups. This cohort had a number of adverse prognostic features: patients were predominantly PS 1-2; the majority had multifocal disease with the largest lesion being >5 cm; and macroscopic vascular invasion, metastases, and AFP >,000 ng ml(-1), were each present in one-third of cases. The median time from application to funding decision was 17 days (range 3-260 days). For the primary 'intention-to-treat' analysis, median overall survival was 4.1 months when funding was declined, and 9.5 months when funding was approved (hazard ratio (HR) 0.48; 95% CI 0.3186-0.7267; P=0.0005). CONCLUSION: These data support the use of sorafenib for patients with advanced HCC as an effective intervention. In the United Kingdom, this applies to a relatively small group of patients, estimated to total ∼800 per year who, unfortunately, do not survive long enough to themselves lobby for the availability of this drug. These data provide a comparison of sorafenib with supportive care and demonstrate the potential detrimental impact on patient outcomes of rationing health-care resources on the basis of cost.

en
dc.format.extent888 - 890en
dc.languageengen
dc.language.isoengen
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectAntineoplastic Agentsen
dc.subjectCarcinoma, Hepatocellularen
dc.subjectCohort Studiesen
dc.subjectFemaleen
dc.subjectHealth Care Rationingen
dc.subjectHumansen
dc.subjectLiver Neoplasmsen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectNeoplasms, Multiple Primaryen
dc.subjectNiacinamideen
dc.subjectPhenylurea Compoundsen
dc.subjectRetrospective Studiesen
dc.subjectSorafeniben
dc.subjectUnited Kingdomen
dc.subjectYoung Adulten
dc.titleSorafenib for advanced hepatocellular carcinoma (HCC): impact of rationing in the United Kingdom.en
dc.typeJournal Article
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/23880824en
plymouth.issue4en
plymouth.volume109en
plymouth.publication-statusPublisheden
plymouth.journalBr J Canceren
dc.identifier.doi10.1038/bjc.2013.410en
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine/UoA01 Clinical Medicine
dc.publisher.placeEnglanden
dcterms.dateAccepted2013-07-01en
dc.identifier.eissn1532-1827en
dc.rights.embargoperiodNot knownen
rioxxterms.versionofrecord10.1038/bjc.2013.410en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2013-08-20en
rioxxterms.typeJournal Article/Reviewen


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV