The FDA just approved two more melanoma therapeutics.
They state:
The U.S. Food and Drug Administration today approved two new drugs,
Tafinlar (dabrafenib) and Mekinist (trametinib), for patients with
advanced (metastatic) or unresectable (cannot be removed by surgery)
melanoma, the most dangerous type of skin cancer.
Tafinlar, a BRAF inhibitor, is approved to treat patients with
melanoma whose tumors express the BRAF V600E gene mutation. Mekinist, a
MEK inhibitor, is approved to treat patients whose tumors express the
BRAF V600E or V600K gene mutations. Approximately half of melanomas
arising in the skin have a BRAF gene mutation. Tafinlar and Mekinist are
being approved as single agents, not as a combination treatment.
The
FDA approved Tafinlar and Mekinist with a genetic test called the THxID
BRAF test, a companion diagnostic that will help determine if a
patient’s melanoma cells have the V600E or V600K mutation in the BRAF
gene.
The FDA is rapidly issuing approvals on many of these therapeutics.
Cost and long term efficacy are still issues.