DID YOU KNOW?
- If melanoma is detected early, it can usually be successfully treated1
- One in 55 people will be diagnosed with melanoma during their lifetime1
- More than 68,000 new cases of melanoma were diagnosed in 2010 – nearly 8,700 resulted in death2
- 5-10% of melanoma is inherited3,4
- MELARIS® is a test for hereditary melanoma
Hereditary melanoma is a condition that causes an increased risk for melanoma, and in some families, an increased risk for pancreatic cancer. The most common known cause of hereditary melanoma is a mutation in the p16 gene.
RED FLAGS: IDENTIFYING THOSE WHO MAY BE AT RISK
Please use the following questions to help identify those who may be at risk for hereditary melanoma*:
- Have you or a family member had two or more melanomas at any age?
- Have you or anyone in your family been diagnosed with melanoma and pancreatic cancer at any age?
- Has anyone in your family ever tested positive for a known p16 germline mutation?
If you would like more information on hereditary melanoma, click here.
If you would like to order patient materials, click here.
THE ABCDEs OF MELANOMA
Potential signs of melanoma – look for moles with one or more of the following characteristics:
*Assessment criteria based on scientific literature and expert opinion. For a list of references go to www.myriadpro.com/references.
3. Hayward NK, Oncogene. 2003;22(20):3053-62.
4. Hansen CB, et al. Lancet Oncol. 2004;5(5):314-9.