OncoExTra® test
Don't miss half the genomic story. Personalize your advanced cancer care with ultra-comprehensive genomic profiling.
The full genomic story requires more than DNA alone
Interrogating both DNA and RNA in a single test, the OncoExTra test provides ultra-comprehensive genomic profiling that thoroughly detects clinically actionable mutations and fusions across each patient’s whole-exome (DNA) and whole-transcriptome* (RNA).1
Uncover more variants. Find more useful targets.
- Ultra-comprehensive genomic profiling across nearly 20k genes in both tumor DNA + RNA, ensuring all possible genes are evaluated for genomic alterations upfront1
- Broad and deep sequencing coverage accurately detects mutations, rare fusions, and transcript variants1
- Patient-matched tumor-normal sequencing provides gold standard TMB calculation2 and allows for differentiation between germline and somatic variants
- Optional immunohistochemical (IHC) panels and single stains provide an added level of detail†
The OncoExTra test may be right for
your patient whose cancer is:
of patients who receive
the
OncoExTra® test
have $0 in
out-of-
pocket costs3
of patients have a
financial responsibility
of <$1003
The OncoExTra report:
putting a spotlight on what matters most
The easy-to-interpret report highlights the most actionable insights first for timely, shared decision-making:
- Mutations and fusions associated with FDA-approved therapies deliver a comprehensive genomic picture‡
- Immuno-oncology signatures (TMB/MSI) support personalized therapy selection
- Clinical trial options to help inform next steps
Fax your order
* Whole-transcriptome with select variants reported in New York State
† IHC testing not currently available in New York State
‡The OncoExTra test was developed, and the performance characteristics validated by Genomic Health, Inc., a wholly-owned subsidiary of Exact Sciences Corporation following College of American Pathologists (CAP) and Clinical Laboratory Improvement Amendments (CLIA) regulations. The OncoExTra test is performed at the Genomic Health Phoenix clinical laboratory. Exact Sciences clinical laboratories are accredited by CAP, certified under CLIA regulations, and qualified to perform high-complexity clinical laboratory testing. This test has not been cleared or approved by the US Food and Drug Administration.
MSI, microsatellite instability; TMB, tumor mutational burden
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References