Today, Bristol-Myers Squibb is pleased to welcome the decision by The National Institute for Health and Clinical Excellence (NICE) to recommend Yervoy (ipilimumab) for the treatment of previously-treated advanced (unresectable or metastatic) melanoma within the Final Appraisal Determination (FAD). This landmark announcement will enable patients in England and Wales suffering from this terminal illness to routinely access treatment with ipilimumab - the first treatment to demonstrate improved survival for patients with advanced melanoma and the first medicine to be licensed in the UK for the treatment of this disease since dacarbazine in the 1970s.2 Bristol-Myers Squibb have collaborated closely with NICE over the past year and the Company is pleased to have met all the clinical and economic requirements needed to reach today's positive recommendation.
"Today's decision is very welcome news and marks a major milestone in the treatment of advanced melanoma," said Dr. Paul Lorigan, Senior Lecturer in Medical Oncology, the Christie NHS Foundation Trust. "Ipilimumab's potential to provide a long-term survival benefit in some patients makes it an important treatment option and represents a genuine step change in the management of this disease."
Within its appraisal NICE acknowledged that ipilimumab represented a step-change in the treatment of advanced melanoma, a generally fatal disease with a median overall survival of just 6 to 9 months.3 In ipilimumab's pivotal Phase III clinical trial, published in The New England Journal of Medicine, 46% (63 people out of 137) of patients were still alive at one year in the ipilimumab arm and 25% (34 people out of 136) in the comparator arm, a vaccine called gp100. The median overall survival was 10.1 months among patients receiving ipilimumab alone, compared to 6.4 months among patients receiving gp100 alone.4 In some patients treated with ipilimumab long-term survival has been observed, with over 4.5 years of follow-up.5 The safety profile of ipilimumab is considered to be related to its mechanism of action as an immunotherapy. Immune-related adverse reactions, which can be severe or life threatening, may involve the gastrointestinal, liver, skin, nervous, endocrine, or other organ systems. Early diagnosis and appropriate management of adverse events using established product-specific guidelines are essential to minimise complications.
Commenting on NICE's decision, Gill Nuttall, Factor 50, said "Today's decision by NICE is very welcome news for patients with advanced melanoma, who have waited such a long time for any new treatment options that have the potential to extend life. The important thing now will be for positive guidance to be implemented as soon as possible so that suitable patients can be given a chance to benefit from this treatment."