Why PathVysion may be right for your patients
The PathVysion HER-2 DNA probe kit is one of the first examples of what is recognized as genomic disease management, or personalized medicine - meaning that the test enables the accurate assessment of a patient's HER-2 status at the DNA level and guides doctors to make the most appropriate therapy decisions based on the patient's own genetic profile.
PathVysion is approved by the U.S Food and Drug Administration (FDA) for three claims: prognosis, adriamycin-based chemotherapy selection, and Herceptin® (Trastuzumab) monoclonal antibody therapy selection.
PathVysion is the best test for assessing HER-2 status:
- Patients with gene amplification by PathVysion have greater responsiveness to Herceptin than patients with overexpression by IHC;1,2
- FISH is considered the gold standard for HER-2 testing3; and
- Studies indicate superiority of FISH to accurately and reproducibly assess tumors for HER-2 status.4
PathVysion direct labeled FISH probes yield definitive results at the molecular level. The test uses fluorescent probes to "paint" the HER-2 genes in the tumor cell nucleus, to see if the number of gene copies is normal or not. Interpretation is objective - results are obtained by counting the fluorescent signals (dots). In addition, because this test measures genetic material, which is very stable, tissue preparation has very little effect on test outcome.
1Vogel C, et al. Superior outcomes with Herceptin (Trastuzumab) in FISH selected patients. Proc Am Soc Clin Oncol. 2001: 20:22a. Abstract 86 and Presentation.
2Mass R, et al. Evaulation of Clinical Outcomes According to HER-2 Detection by Fluorescence in situ Hybridization in Women with Metastatic Breast Cancer Treated with Trastuzumab. Clnical Breast Cancer, vol 6, No. 3, 240-246, 2005.
3National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology, Breast Cancer V.I.2007.
4Press M, et al. Diagnostic Evaulation of Her-2 as a Molecular Target: An Assessment of Accuracy and Reproducibility of Laboratory Testing in Large, Prospective Randomized Clinical Trials, Clinical Cancer Research 2005; 11(18) September 15, 2005.
