Cancer is a disease of the genome. Genomic testing provides valuable insights that determine if patients can benefit from targeted treatment based on the genomic makeup of their tumors.
In a broad sense, there are two types of genomic tests for cancer:
Singleplex tests examine one potential genomic alteration at a time.
Multiplex tests utilize a single process to simultaneously examine numerous potential genomic alterations, thereby providing a larger genomic profile of the cancer in one test.
Multiplex tests can be clinically valuable as they allow clinicians to obtain comprehensive information on a large number of genes from the scarce sample of tumor tissue. In recent years, multiplex genomic testing has become increasingly popular in cancer treatment as it provides the most comprehensive understanding the unique genomic alterations of each individual tumor. By knowing the underlying genomics of each cancer patient, doctors can quickly move patients to the right therapies, identify new molecular targets worthy of novel drugs, and test novel drugs in the right study subjects.
In order to identify and enroll the patients most appropriate for our investigational therapies, we are working with clinical, laboratory and molecular pathology partners who integrate multiplex genomic testing into their routine clinical practice. We are also partnering with leading diagnostic companies to develop and commercialize companion diagnostic tests for our programs. Through a collaboration with Illumina, Inc. we are developing a next-generation sequencing (NGS) based companion diagnostic (CDx) for detecting NTRK gene fusions, and RET gene alterations, across tumor types. We are working with Ventana Medical Systems, Inc. to develop a pan-TRK immunohistochemistry (IHC) test to identify patients across tumor types with NTRK gene fusions.