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      Sorafenib for advanced hepatocellular carcinoma (HCC): impact of rationing in the United Kingdom

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          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 >1000 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.

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          Rising incidence of hepatocellular carcinoma in the United States.

          Clinical observations have suggested that the number of cases of hepatocellular carcinoma has increased in the United States. We analyzed data from the Surveillance, Epidemiology, and End Results (SEER) data base to determine the age-adjusted incidence of hepatocellular carcinoma from 1976 to 1995, data from the U.S. vital-statistics data base to determine age-adjusted mortality rates from 1981 to 1995, and data from the Department of Veterans Affairs to determine age-adjusted rates of hospitalization for the disease from 1983 to 1997. The incidence of histologically proved hepatocellular carcinoma increased from 1.4 per 100,000 population (95 percent confidence interval, 1.3 to 1.4) for the period from 1976 to 1980 to 2.4 per 100,000 (95 percent confidence interval, 2.3 to 2.4) for the period from 1991 to 1995. Among black men, the incidence was 6.1 per 100,000 for the period from 1991 to 1995, and among white men, it was 2.8 per 100,000. There was a 41 percent increase in the mortality rate from primary liver cancer and a 46 percent increase in the proportion of hospitalizations attributable to this disease during the periods studied. The incidence increased significantly among younger persons (40 to 60 years old) during the period from 1991 to 1995 as compared with earlier periods. An increase in the number of cases of hepatocellular carcinoma has occurred in the United States over the past two decades. The age-specific incidence of this cancer has progressively shifted toward younger people.
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            Author and article information

            Journal
            Br J Cancer
            Br. J. Cancer
            British Journal of Cancer
            Nature Publishing Group
            0007-0920
            1532-1827
            20 August 2013
            23 July 2013
            : 109
            : 4
            : 888-890
            Affiliations
            [1 ]Cancer Research UK Centre, University of Liverpool , Daulby Street, Liverpool L69 3GA, UK
            [2 ]Cancer Research UK, School of Cancer Sciences, University of Birmingham , Vincent Drive, Edgbaston, Birmingham B15 2TT, UK
            [3 ]King's College Hospital and Guy's and St Thomas' NHS Foundation Trusts , London, UK
            Author notes
            [4]

            DHP and SAH contributed equally to this work

            Article
            bjc2013410
            10.1038/bjc.2013.410
            3749577
            23880824
            f4936719-f556-454e-9489-db5c942758cc
            Copyright © 2013 Cancer Research UK

            From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

            History
            : 11 April 2013
            : 10 June 2013
            : 01 July 2013
            Categories
            Clinical Study

            Oncology & Radiotherapy
            sorafenib,multikinase inhibitor,advanced hepatocellular cancer,primary care trusts,health-care rationing,supportive care

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