The GeneSearch™ Breast Lymph Node Assay - the first FDA-approved molecular diagnostics
assay for breast lymph node testing represents a potentially new standard of care
in intra-operative breast lymph node testing, offering the chance for:
- fewer second surgeries and hospital stays
- improved overall quality of patient care
- rapid, reproducible, objective results
- detection of metastases greater than 0.2 mm
- analyze up to 50% of the lymph node
For a complete list of materials required to run the GeneSearch™ BLN Assay please refer to the Instructions for Use (IFU)
The GeneSearch™ Breast Lymph Node (BLN) Assay may be used in conjunction with sentinel
lymph node biopsy for a patient who has been counseled on use of this test and has
been informed of its performance. False positive results may be associated with
increased morbidity. False negative and inconclusive test results may be associated
with delayed axillary node dissection. Clinical studies so far are inconclusive
about a benefit from treatment based on findings of breast cancer micrometastases
in sentinel lymph nodes.
Intended Use
For in vitro diagnostic use only.
The GeneSearch™ Breast Lymph Node (BLN) Assay is a qualitative, in vitro diagnostic
test for the rapid detection of greater than 0.2 mm metastases in nodal tissue removed
from sentinel lymph node biopsies of breast cancer patients. Results from the assay
can be used to guide the intra-operative or post-operative decision to remove additional
lymph nodes.
Post-operative histological evaluation of permanent sections of the tissue specimen,
in accordance with usual diagnostic practice and using the Veridex lymph node cutting
scheme, is required.
For complete information on Intended Use, Warnings and Precautions, and Limitations,
see the Instructions
for Use (IFU).
This information is intended for use by our customers, patients and healthcare professionals
in the United States only. Veridex recognizes that the internet is a global communications
medium; however, laws, regulatory requirements and medical practices for in vitro
diagnostic devices vary from country to country. The information included here may
not be appropriate for use outside the United States. Product availability is subject
to local regulatory authority approvals.
GeneSearch™ is a trademark of Veridex, LLC.