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Back to Test Catalogue
Test ID: ADAIBD S

Adalimumab Level and Anti-Drug Antibody for IBD, Serum

Test Overview

Clinical Utility

The American Gastroenterological Association recommends optimal adalimumab trough concentration of 7.5 mcg/mL or greater in patients with active IBD. Data from separate clinical studies suggest an optimal adalimumab trough concentration greater than 4.5 mcg/mL or 8-12 mcg/mL. Sub-therapeutic adalimumab levels may be due to a patient not yet achieving a steady state trough level early in therapy, inadequate dosing, a dosing interval that is too long, or accelerated adalimumab clearance. Accelerated adalimumab clearance may be explained by the presence of adalimumab anti-drug antibody or rheumatoid factor in the patient’s serum, or may be caused by other diseases that indirectly lead to immunoglobulin loss (i.e. kidney disease, protein-losing gastroenteropathy).

  • If adalimumab level is sub-therapeutic but total adalimumab anti-drug antibody is not detected: Patients with a sub-therapeutic adalimumab trough level, but no anti-drug antibody, may benefit from an increased adalimumab dose.
  • If adalimumab level is sub-therapeutic and total adalimumab anti-drug antibody is detected: Detectable serum adalimumab anti-drug antibody may cause accelerated adalimumab clearance leading to reduced trough levels and a compromised clinical response. Such patients are more likely to benefit from a switch in biologic therapy than from an increase in adalimumab dose.
  • If adalimumab level is therapeutic and total adalimumab anti-drug antibody is not detected: In patients who do not respond or who lose their clinical response, mucosal inflammation is likely to be driven by a process that is not TNF alpha dependent. A switch to a different class of therapy should be considered.
  • If adalimumab level is therapeutic and total adalimumab anti-drug antibody is detected: If the patient is responding clinically, the detected anti-drug antibody may not be clinically significant because the detected anti-drug antibody may not be functional or the level is inadequate to accelerate adalimumab clearance. Anti-drug antibody may disappear over time or increase, and, if increased, may cause sub-therapeutic adalimumab levels and a loss of response in the future. Patients with a loss of adalimumab response despite therapeutic trough levels may benefit from a switch to a different class of therapy.

Method

Enzyme-linked immunosorbent assay (ELISA)

Aliases/Synonyms

TNF Inhibitor Antibody; Anti-TNF Inhibitor Antibody; Anti-Humira ® Antibody; Humira ® Anti-drug Antibody

Specimen

Specimen Type

Avoid gel-separator tubes
Serum

Important Note: TEST ID ADAIBD S
Non-interfaced clients should specify the Test ID ADAIBD S when ordering this test. Not doing so will cause processing delays while ICL ascertains which test you are requesting - please refer to the notes below.
A similar test is offered by this lab:
Adalimumab Level and Anti-Drug Antibody for Rheumatic Diseases, Serum

Containers

Collection Containers

Red top (no additive)

Volume

Sample Volume

2 mL

Minimum Volume

1 mL

Specimen Comment

Avoid gel separator tubes.

Patient Preparation

Refrain from taking biotin supplements or biotin containing vitamins 24 – 48 hours before blood draw .

Collection & Handling

Collection Instructions

Blood should be drawn just before the next infusion of adalimumab to measure the trough drug level.

Handling Information

Store and send frozen.

Stability

Ambient Refrigerated Frozen
48 hours 7 days 42 days

Rejection Criteria

Criteria Specification
Hemolysis Gross
Specimen Gel-separator tubes

Performance & Interpretation

Turnaround Time

10 days

Results

Name
Units
Reference Range
Conversion
  1. Adalimumab Level, IBD
    µg/mL
  2. Adalimumab AB, IBD
    AU
    < 10
  3. Interpretation
    See Note

    Comment

    The American Gastroenterological Association recommends optimal adalimumab trough concentration of 7.5 mcg/mL or greater in patients with active IBD. Data from separate clinical studies suggest an optimal adalimumab trough concentration greater than 4.5 mcg/mL or 8-12 mcg/mL. Subtherapeutic adalimumab levels may be due to a patient not yet achieving a steady state trough level early in therapy, inadequate dosing, a dosing interval that is too long, or accelerated adalimumab clearance. Accelerated adalimumab clearance may be explained by the presence of adalimumab anti-drug antibody or rheumatoid factor in the patient's serum or may be caused by other diseases that indirectly lead to immunoglobulin loss (i.e., kidney disease, protein-losing gastroenteropathy).

    • If adalimumab level is subtherapeutic but total adalimumab anti-drug antibody is not detected: Patients with a subtherapeutic adalimumab trough level, but no anti-drug antibody, may benefit from an increased adalimumab dose.
    • If adalimumab level is subtherapeutic and total adalimumab anti-drug antibody is detected: Detectable serum adalimumab anti-drug antibody may cause accelerated adalimumab clearance leading to reduced trough levels and a compromised clinical response. Such patients are more likely to benefit from a switch in biologic therapy than from an increase in adalimumab dose.
    • If adalimumab level is therapeutic and total adalimumab anti-drug antibody is not detected: In patients who do not respond or who lose their clinical response, mucosal inflammation is likely to be driven by a process that is not TNF alpha dependent. A switch to a different class of therapy should be considered.
    • If adalimumab level is therapeutic and total adalimumab anti-drug antibody is detected: If the patient is responding clinically, the detected anti-drug antibody may not be clinically significant because the detected anti-drug antibody may not be functional or the level is inadequate to accelerate adalimumab clearance. Anti-drug antibody may disappear over time or increase, and, if increased, may cause subtherapeutic adalimumab levels and a loss of response in the future. Patients with a loss of adalimumab response despite therapeutic trough levels may benefit from a switch to a different class of therapy.

    This information is provided for informational purposes only and is not intended as medical advice. A physician's test selection and interpretation, diagnosis, and patient management decisions should be based on his/her education, clinical expertise, and assessment of the patient.
    The treating healthcare professional should refer to the manufacturer's approved labeling for prescribing, warnings, side effects and other important information.

Referral Location

Out-of-Country

Interface & Setup

HL7 Interface Codes

Order Code Result Name Result Codes Units
ADAIBD S ADALIMUMAB LEVEL, IBD 63378 ug/mL
ADALIMUMAB AB, IBD 63376 AU
INTERPRETATION 63377
COMMENT 63379

Test Version

Last Updated

2023-01-24