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For Patients
Prepare for visits with your doctor or a genetic counselor by learning about testing.
Integrated Oncology Highlights
Every patient comes from a different background with a unique personal and family history. Patients with a family history that is specific to one cancer type may receive more benefit from a focused hereditary panel test. Integrated Oncology offers several cancer panel options for a more targeted approach to testing. Click here to view the press release.
Integrated Oncology now offers the FDA-approved cobas EGFR mutation test V2 in both FFPE tissue and plasma samples
This test was recently FDA-approved as a complementary diagnostic assay that may help identify patients with locally advanced or metastatic urothelial carcinoma more likely to respond to treatment with TecentriqTM(atezolizumab).
This test was recently FDA approved as a companion diagnostic assay to aid in identifying metastatic NSCLC patients for treatment with KEYTRUDA® (pembrolizumab).
This test was recently FDA-approved as a complementary diagnostic test to help physicians determine which patients may benefit most with OPDIVO® (nivolumab).
Prosigna Breast Cancer Prognostic Gene Signature Assay, which is based on the PAM50 gene signature, is an FDA 510(k) cleared assay to assess a patient’s risk of distant recurrence of disease.
IntelliGEN® Oncology Therapeutic Panel (NGS) assay provides an assessment of targetable mutations within a panel of cancer genes known to be involved in the development, progression and/or treatment of cancers.