UGT1A1 Assay
Order Name
UGT1A1
Test Number: 9103375
Revision Date 09/17/2009
Test Number: 9103375
Revision Date 09/17/2009
Test Name | Methodology | LOINC Code |
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UGT1A1 Assay
|
Signal Amplification, Invader chemistry detection |
SPECIMEN REQUIREMENTS | ||||
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Specimen | Specimen Volume (min) | Specimen Type | Specimen Container | Transport Environment |
Preferred | 5 (3 mL) | Whole Blood | EDTA (Lavender Top) | Room Temperature |
Instructions | Keep specimen as whole blood at room temperature. Do not centrifuge, do not refrigerate. Specimen cannot be shared with other testing for risk of DNA contamination. |
GENERAL INFORMATION | |
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Testing Schedule | Assay Dependant |
Expected TAT | 3-10 Day |
Clinical Use | This is a pharmacogenomic assay for identifying subsets of patients at increased risk for toxicity to Irinotecan (CAMPTOSAR®). Irinotecan (CAMPTOSAR®) is used as part of a first line regimen in treating patients with metastatic colon or rectal carcinoma. |
CPT Code(s) | 83891; 83896x20; 83892x8; 83903x4; 83912; 8391226 |
Internal Comments | Deactivated in Sept 2009 due to low utilization - per Sonja Mathews |
Lab Section | Immunology - Serology |