Hepatitis C Virus (HCV) NS5B Drug Resistance for Genotype 1b
The Hepatitis C Virus (HCV) NS5B Drug Resistance for Genotype 1b assay detects NS5 (nonstructural protein 5B) mutations and polymorphisms in HCV genotype 1b that are associated with resistance to direct-acting antivirals: dasabuvir, sofosbuvir (Sovaldi®) and other antiviral combination therapies. The assay is intended to be used for patients with HCV viral loads who are being screened prior to treatment with the direct-acting HCV antivirals, or during treatment with these antivirals when drug resistance is suspected.
ProcedureThe HCV NS5B Drug Resistance assay utilizes RT-PCR amplification with primers in highly conserved viral genomic regions to amplify HCV genotype 1b. The fragments are purified and sequenced using sequencing primers from conserved regions of the fragments. The sequence is compared to a database of mutations associated with antiviral resistance. This test has not been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
4-11 business days from receipt of specimen.
| Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
|---|---|---|---|---|---|---|
| Plasma (1) | 30501 | 87902 | Yes | 3 mL (min. 1 mL/viral load of 1000 IU/mL) |
Resistant/Not Detected |
|
| Serum (1) | 30501 | 87902 | Yes | 3 mL (min. 1 mL/viral load of 1000 IU/mL) |
Resistant/Not Detected |
|
Mutations in the NS5B gene will be reported as Resistant/None Detected. Interpretation of gene mutations and association with antiviral resistance of the relevant antivirals will be listed.
ShippingShip Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor Eurofins test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Viracor Eurofins, 18000 W 99th St. Ste, #10, Lenexa, KS 66219.
Causes for RejectionHCV RNA concentrations too low to allow antiviral resistance testing (see above for minimum volume and viral load), subtypes other than those indicated, whole blood frozen, specimens beyond their acceptable length of time from collection as listed in the specimen handling, or specimen types other than those listed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above. The CPT codes provided are based on Viracor Eurofins interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
ReferencesLavanchy D. 2011. Evolving epidemiology of hepatitis C virus. Clin Microbiol Infect 17:107–115.
Mohd Hanafiah K, Groeger J, Flaxman AD, Wiersma ST. 2013. Global epidemiology of hepatitis C virus infection: new estimates of age-specific antibody to HCV seroprevalence. Hepatology 57:1333–1342.
Smith DB, Bukh J, Kuiken C, Muerhoff AS, Rice CM, Stapleton JT, Simmonds P. 2014. Expanded Classification of Hepatitis C Virus Into 7 Genotypes and 67 Subtypes: Updated Criteria and Genotype Assignment Web Resource. Hepatology 59(1): 318-327.