Irinotecan (Campostar) DNA Test

Is your physician thinking of prescribing Campostar (irinotecan)?

Are you concerned about drug safety?

When patients with a certain genetic variation are given a standard dose of irinotecan, they have a very high risk of severe or even fatal neutropenia, a condition that drastically lowers the ability of the body to fight off infection. This variation is called UGT1A1*28 (UDP-glucuronosyltransferase) and it exists in about 10% of the U.S. population. In 2004, the FDA reviewed the data (click here to learn more about the review process) on UGT1A1*28 and decided that this genetic change should be included in the insert for irinotecan as a risk factor for severe toxicity.

The UGT1A1 Campostar (irinotecan) DNA Drug Reaction Test is considered appropriate for any patient planning to start Campostar (irinotecan) therapy as people with the variation need lower starting doses.

The process is simple. We send a blood or cheek swab collection kit in the mail, and you return samples to our laboratory by overnight courier. Results are typically available within 5 business days.

Ordering Tests

Call Genelex today at 800-523-3080 or order on-line.