Anser VDZ

Overview

  • EPIC Code:
  • MISC
  • Soft Test Code:
  • MSOT
  • Send Out Test Code:
  • 3180
Alternate Names
  • VDZ
  • vedolizumab
Clinical Significance

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 healthcare providers 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.


A quantitative monitoring analysis of VDZ and ATV levels


Specimen Collection & Preparation

Specimen Requirements

 2.0 mL Serum in a SST Gold Top Tube


Alternate Specimen

 2.0 mL Serum from a Red Top Tube in a Plastic Vial


TransportAndStorage

7 days Ambient
9 days Refrigerated


Collection Instructions


Minimum Volume


Neonatal Volumne

Clinical Interpretation

Reference Range:

Serum vedolizumab concentration (VDZ) <1.6 ug/ml 

 
Antibodies to vedolizumab (ATV) concentration <1.6 U/ml


Methodology:
  • Antidrug Antibody Quantification

Clinical Significance

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 healthcare providers 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.


A quantitative monitoring analysis of VDZ and ATV levels


Documentation

 Quantitative assay that simultaneously measures serum vedolizumab (VDZ) and antibodies to vedolizumab (ATV) concentrations


Production Schedule

Sites Performed
  • Prometheus
Departments
  • Sendouts - Miscellaneous
Turn Around Time

3 to 4 days


Coding & Compliance

CDM

00913334


CPT Coding

80280, 82542