These Three Products Now Represent Over Two-Thirds of Patients Treated in the First Line, According to a New Report from BioTrends Research Group
May 10, 2012 – Exton, Penn. -
BioTrends Research Group, one of the world’s leading research and advisory firms for specialized biopharmaceutical issues, has released findings from the second wave of its LaunchTrends® Yervoy and Zelboraf
report, in which 103 U.S.-based medical oncologists were surveyed about their current and expected treatment patterns in advanced melanoma. A key finding from this study is that medical oncologists have positive patient treatment experiences with these agents, so they are planning on utilizing them more often when treating advanced melanoma.
Medical oncologists were interviewed about Bristol-Myers Squibb’s Yervoy (ipilimumab) one year after launch and Genentech/Roche’s Zelboraf (vemurafenib) six months after launch. For both Yervoy and Zelboraf the vast majority of medical oncologists have adopted these brands and both brands have seen the average number of patients on therapy increase by at least one third since the last wave of research conducted six months ago. These products, which have very different mechanisms of action, are seen as significant treatment progress for advanced melanoma.
Yervoy is one of the first targeted immunotherapies in cancer and over two-thirds of medical oncologists report efficacy as a key advantage of this therapy with the survival data most often cited. However, medical oncologists report a key disadvantage of this therapy over currently available agents is the unique side-effects related to an immunotherapy; although after one year on the market they report being able to frequently manage these side-effects. Surveyed specialists also noted that the response rates for Yervoy are often unpredictable, but when it does work efficacy can be sustained.
Zelboraf is indicated for advanced melanoma that has the BRAF positive gene mutation, making it the first personalized medicine in the treatment of melanoma. The percent of patients screened for the BRAF mutation increased from the previous wave of research and now represents over two-thirds of melanoma patients. Medical oncologists report a key stated advantage of Zelboraf over currently available agents is efficacy, with an emphasis on the high response rates. A key disadvantage of this therapy is that it cannot be used in patients without the BRAF mutation (i.e. wild type patients) and it may cause cutaneous squamous cell carcinoma (cuSCC), although it usually does not spread to other parts of the body.
In terms of level of interest with late stage products in development for advanced melanoma, medical oncologists were most interested in Yervoy in combination with another agent such as Zelboraf, Merck & Co.’s Temodar or generic dacarbazine. Medical oncologists also had a high interest level in Celgene’s Abraxane combined with Genentech’s Avastin.
“Medical oncologists report that they have seen significant clinical benefits in other types of cancer when using combination therapies; they report that combination therapy can hit cancer at two different pathways which inhibits the development of resistance a major issue in the treatment of cancer,” said BioTrends Oncology Therapeutic Director Dan Winkelman.
LaunchTrends: Yervoy and Zelboraf
is a series of three post-launch syndicated reports designed to track the uptake of Yervoy and Zelboraf following their commercial availability. Wave 1 tracked the uptake of Yervoy six months post-launch and Zelboraf at launch while subsequent waves are fielded every six months to monitor the competitive dynamics of these therapies. For this report, BioTrends surveyed 103 medical oncologists and conducted qualitative interviews with a subset of 15 of the respondents in April 2012. BioTrends will continue to track the uptake of Yervoy and Zelboraf in a subsequent wave in this report series which will be fielded in October 2012.