Colorectal Cancer : NRAS Variant Analysis

Test Information

KRAS: Mutations in exon 2 of KRAS are reported in 40% of CRC with codon 12 and 13 identified as the two hotspots accounting for about 95% of all mutation types. These presence of these mutations predict a lack of response to EGFR inhibitors cetuximab and panitumumab therapies (The Lancet Oncology (2014) 15(10): 1065-75; New England Journal of Medicine (2013) 369(11) 1023-34). Based on the clinically available information, the National Comprehensive Cancer Network (NCCN) recommends all patients with metastatic colorectal cancer have KRAS/NRAS genotyping and, if positive, to not be treated with EGFR inhibitors (cetuximab or panitumumab).

Turnaround Time

5 days

CPT Code(s)

81311

Cost

$350

Genes

Indications

Gene sequencing and targeted mutation testing and copy number analysis can serve as a useful diagnostic and potentially prognostic tool for the analysis of affected tissues or tumors. The detection of copy number variants or specific gene mutations may enhance treatment decisions.

Specimen Requirements

Analysis can be performed on fresh or frozen tissue samples as well as formalin-fixed, paraffin-embedded tissue samples.

Transport Instructions

The specimen should be kept at the appropriate temperature and delivered via overnight shipping.

Have Questions Need Support?

Call our laboratory at 1-800-473-9411 or contact one of our Laboratory Genetic Counselors for assistance.
Robin Fletcher, MS, CGC
Kellie Walden, MS, CGC

Oncology Testing, Targeted Variants
One Mother's Story

One Mother's Story

After a long three-year struggle trying to have children, our son, Charlie, was born on April 18, 2009. He was our miracle...perfect in every way! When Charlie was five days old, our pediatrician called to notify us that one of the numbers from the heel prick test was a bit high. We headed to the hospital that afternoon for more tests. I will never forget the following day. It was cool and crisp - not a cloud in the sky....

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