Prometheus Anser VDZ
Test Mnemonic
ANSVDZ
CPT Codes
- 80280 - QTY (1)
- 82542 - QTY (1)
Includes
- Serum vedolizumab (VDZ) concentration
- Antibodies to vedolizumab (ATV) concentration
Performing Laboratory
Prometheus
FDA Category
Laboratory Developed Test
Specimen Requirements
Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
---|---|---|---|---|---|
2 mL | Serum | SST (Gold) | Refrigerated | Ship using cold pack |
Alternate Specimen Requirements
Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
---|---|---|---|---|---|
2 mL | Serum | No additive (Red) | Refrigerated | Ship using cold pack |
Minimum Specimen Requirements
Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
---|---|---|---|---|---|
2 mL | Adult patients | ||||
0.5 mL | Pediatric patients |
Stability
Environmental Condition | Description |
---|---|
Ambient | 7 days |
Refrigerated | 9 days |
Frozen | Unacceptable |
Days Performed
Varies
Turnaround Time
4 - 5 days
Methodology
Name | Description |
---|---|
High Performance Liquid Chromatography (HPLC) |
Clinical Info
Serum concentrations of vedolizumab (VDZ) may vary among equally dosed patients, which can ultimately affect patient outcomes. Some patients may develop immunogenicity to VDZ by producing antibodies to vedolizumab (ATV), and the presence of persistent anti-vedolizumab antibody has been observed to substantially reduce serum concentrations of vedolizumab. The quantitative measurement of VDZ and ATV levels in serum provides clinicians with valuable information to help them gain a better understanding of the factors that may be affecting a patient’s loss of response. The Prometheus Anser VDZ test is a next generation and more sensitive quantitative monitoring assay that allows healthcare providers to measure and monitor serum VDZ and ATV levels at any time during therapy. Incorporating therapeutic drug monitoring may clarify what factors are contributing to a patient’s loss of response and help guide treatment decisions by providing information to help determine an appropriate course of action.