Our Unique Approach—Targeted analysis of cancer-Related Genes
Foundation Medicine provides analysis of tumors to help better identify cancer subtypes – and help oncologists develop personalized treatment strategies for cancer patients.
Molecular testing by Foundation Medicine provides precise genomic information about your cancer in a way never before available.
Advanced molecular testing method
Foundation Medicine uses a sophisticated laboratory method called massively parallel sequencing to perform molecular analysis on tumor biopsy samples.
All of the most relevant cancer-related genes are examined within 2-3 weeks and with great precision. Our test is optimized to identify the somatic alterations in your cancer tissue.
Any type of cancer, all cancer-related genomic defects
Foundation Medicine’s diagnostic test is unlike other available tests. It looks for all of the alterations present in any type of solid tumor, using a very small amount of biopsy tissue, to perform extensive analysis of relevant cancer-related genes.
Many available molecular tests are designed for testing only certain types of cancer. They detect only a few specific alterations that occur at high frequency in those tumor types.
Our test gives your doctor the opportunity to find many more relevant genomic alterations in your cancer than is provided by other available methods.
Comprehensive analysis and results
Your results are presented to your oncologist along with interpretive information drawn from a knowledge base of publicly available scientific and medical literature, clinical trials, and genomic research. This helps your oncologist make individualized treatment recommendations specific to you and optimize your overall cancer treatment plan.
Commercial Availability
Foundation Medicine’s comprehensive cancer genomics test will be launched nationally mid-2012.

