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Test Code LABFCERT Certolizumab and Anti-Certolizumab Antibody, DoseASSURE CTZ

Additional Codes

Test Name in EPIC EPIC Test Code Mnemonic Mayo Test ID

Certolizumab pegol and Anti-Certolizumab Antibodies

LABFCERT FCZAC FCZAC

 


Specimen Required


Specimen Type: Serum

Container/Tube: Red or SST

Specimen Volume: 2 mL

Collection Instructions: Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 2 mL of serum frozen in a plastic vial.

To avoid delays in turnaround time when requesting multiple tests, please submit separate frozen specimens for each test requested.


Useful For

Provides certolizumab drug concentration and anti-certolizumab antibodies in order to optimize treatment and facilitate clinical decision-making.

 

This assay may be helpful in any patient on certolizumab therapy for Crohn's disease, psoriasis, or other autoimmune condition.

Method Name

Electrochemiluminescence immunoassay (ECLIA); Surface Plasmon Resonance

Reporting Name

Certolizumab and Anti-Certo Ab

Specimen Type

Serum

Specimen Minimum Volume

0.60 mL (Note: This volume does not allow for repeat testing.)

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Frozen (preferred) 14 days
  Refrigerated  14 days

Reject Due To

Gross hemolysis Gross reject; Mild OK
Gross lipemia Reject
Gross icterus NA
Other/Tissue/Swab Specimens other than indicated

Reference Values

Certolizumab:

Quantitation Limit: <1.0 ug/mL

 

Results of 1 ug/mL or higher indicate detection of certolizumab

 

Anti-Certolizumab Antibody:

Quantitation Limit: <40 ng/mL

 

Results of 40 ng/mL or higher indicate detection of anti-certolizumab pegol antibodies.

Cautions

As with other biologics, the optimal certolizumab concentration depends upon patient-specific factors including co-morbidities, disease, and desired therapeutic endpoint.

 

Trough blood collection (just before the next dose) is suitable because target ranges and therapeutic cut-offs are established by clinical studies that typically evaluate trough concentrations.

 

Therefore, the timing of specimen collection should be considered when interpreting drug concentrations. Drug half-life should be factored in when evaluating non-trough concentrations.

 

Adequate drug trough levels do not guarantee clinical efficacy since primary non-response can be due to mechanistic failure.

 

Lack of clinical response may be due to inadequate drug exposure, immunogenicity or mechanistic mismatch. Positive anti-certolizumab antibodies should be interpreted in the context of the concomitant free certolizumab drug level.

Performing Laboratory

Esoterix Endocrinology

Test Classification

These tests were developed and their performance characteristics determined by LabCorp. They have not been cleared or approved by the Food and Drug Administration.

CPT Code Information

80299

82397

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FCZAC Certolizumab and Anti-Certo Ab Not Provided

 

Result ID Test Result Name Result LOINC Value
Z5637 Certolizumab 87404-0
Z5638 Anti-Certolizumab Antibody 87405-7

Day(s) Performed

Tuesday

Report Available

10-21 days