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NICE recommends eribulin for patients with locally advanced or metastatic breast cancer

3 Nov 2016
NICE recommends eribulin for patients with locally advanced or metastatic breast cancer

The National Institute of Health and Care Excellence (NICE) has recommended eribulin (marketed as Halaven) for the treatment of locally advanced or metastatic breast cancer in a Final Appraisal Determination.

Eribulin is the first breast cancer treatment to be recommended by NICE in nearly a decade.

Eribulin is indicated in the European Union for the treatment of adults with locally advanced or metastatic breast cancer who have progressed after at least one chemotherapeutic regimen for advanced disease.

Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting, unless patients were not suitable for these treatments.

NICE has now recommended eribulin for the treatment of adults with locally advanced or metastatic breast cancer who have progressed after at least two chemotherapeutic regimen for advanced disease. Prior therapy may have included an anthracycline or a taxane, and capecitabine.

Approximately 44,500 women are diagnosed with breast cancer in England each year, of whom one third subsequently develop metastatic disease.

Only 15% of women with metastatic breast cancer will survive beyond five years.

Eribulin is one of the most prescribed treatments within the CDF and to date approximately 4,000 patients have been able to access eribulin in the UK since 2011 .

“I am delighted that women in England with locally advanced or metastatic breast cancer will continue to be able to access eribulin, and that the future of this treatment within the NHS is secure. Eribulin significantly improves overall survival in women with this disease and it is therefore an important option against breast cancer,” comments Dr Mark Harries, Consultant Medical Oncologist.

Eribulin was first approved and launched in the UK in 2011 and marketing authorisation was extended for earlier use in advanced breast cancer from the European Commission on 3 July 2014.

Eribulin is currently approved in more than 60 countries around the world including all of the European Union, Canada, United States, Russia, Switzerland, South Korea, Japan and Singapore.

Source: Eisai