According to a recent
article in Medpage Today, an
estimated 75,000 cases of melanoma are expected to be reported in the United
States in 2012. Considering that melanoma has been tagged as the deadliest form
of cancer, it should be no surprise that there is ongoing research to find a
cure.
In 2011, a BRAF inhibitor
called vemurafenib (marketed as zelboraf), was approved by the FDA after
exhibiting significant increases in the survival rates of patients in the late
stages of melanoma. Prior to zelboraf, dacarbazine was the only treatment
available to those diagnosed with melanoma. However, the medication proved to
be effective in only 7-12 percent of all cases. In addition to increasing a
patient’s chance for survival, zelboraf has also been shown to improve a
patient’s quality of life and self-sufficiency.
Unfortunately, while the
statistics relating to zelboraf are promising, the cost for treatment is
extremely discouraging. Angie King, a PharmD student at Northeastern University
in Boston, has been conducting a budget impact study to determine if the cost
of zelboraf justifies its use in Medicaid programs.
According to King,
conventional treatment with dacarbazine would cost $31,873 per year, whereas a
year of treatment with the traditional drug plus vemurafenib could cost as much
as $314,347. That is a startling difference, but refusing to offer this new
treatment due to cost could raise major ethical questions.
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