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Labcorp Launches Expanded DPYD Test to Identify Cancer Patients at Risk for Severe Chemotherapy Side Effects

Key Takeaway: Labcorp has launched an expanded DPYD Genotyping test to identify cancer patients at risk of severe side effects from fluoropyrimidine chemotherapy. This test detects all DPYD variants recommended by the Association for Molecular Pathology, enabling safer and more personalized treatment. The initiative aims to reduce the risk of severe toxicity and improve patient outcomes in cancer care.
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POSITIVE FACTORS

  • Expanded DPYD test enhances personalized cancer treatment.
  • Identifies patients at risk for severe chemotherapy side effects.
  • Supports safer treatment options and reduces preventable harm.
  • Strengthens Labcorp's pharmacogenomics and oncology portfolio.

Full Press Release Details

New pharmacogenomic test detects all DPYD variants recommended by the Association for Molecular Pathology to support safer, more personalized cancer treatment
BURLINGTON, N.C.,May 28, 2026/PRNewswire/ --Labcorp (NYSE:LH), a global leader of innovative and comprehensive laboratory services, today announced the availability of its expandedDPYD Genotyping testto help identify cancer patients who may be at increased risk for severe or life-threatening side effects from fluoropyrimidine chemotherapy. Labcorp now offers genotype testing for allDPYDTier 1 and Tier 2 variants recommended by theAssociation for Molecular Pathology(AMP).
"Advances in pharmacogenomics are reshaping cancer care," said Marcia Eisenberg, Ph.D., chief scientific officer at Labcorp. "Our expandedDPYDtest identifies patients at risk for severe toxicity before treatment begins, supporting safer, more personalized care. This expansion also strengthens Labcorp's pharmacogenomics and oncology portfolio, complementing the company's hereditary cancer testing, screening, diagnostic and precision oncology offerings to support more personalized cancer care across the patient journey."
Addressing a Significant Risk in ChemotherapySome patients experience preventable severe toxicity and death from chemotherapy intended to treat their cancer. Fluoropyrimidines, including 5-fluorouracil (5-FU) and capecitabine, are chemotherapy agents widely used to treat cancers including colorectal, pancreatic, upper gastrointestinal, breast, and head and neck. However, approximately9%of patients carry aDPYDvariant that can impair their ability to break down these drugs, increasing the risk of severe toxicity, and contributing to an estimated1,300 deathsin the United States each year from 5-FU toxicity.
TheDPYDgene encodes the enzyme DPD, which metabolizes more than80%of 5-FU. Patients with reduced or absent DPD activity can experience serious, potentially life-threatening side effects, including diarrhea, neutropenia and neurotoxicity when exposed to 5-FU or capecitabine.
Updated U.S. Food and Drug Administration (FDA) product labeling for 5-FU and capecitabine includes a Boxed Warning about the risk of severe adverse reactions or death in patients with complete DPD deficiency. The FDA alsoadvisestesting forDPYDvariants before treatment with 5-FU or capecitabine unless immediate treatment is necessary and recommends avoiding use of these drugs in patients with certain homozygous or compound heterozygousDPYDvariants associated with complete DPD deficiency. Recent updates to National Comprehensive Cancer Network (NCCN) guidelines for colon cancer and other relevant indications reference these Boxed Warnings and the recommendation forDPYDtesting. Clinical Pharmacogenomics Implementation Consortium (CPIC) guidelines further recommend adjusting or avoiding treatment based on a patient'sDPYDmetabolizer status as determined byDPYDtesting.
Building on Leadership in PharmacogenomicsLabcorp has offeredDPYDtesting since 2006 and offers pharmacogenomic testing across multiple specialty areas, including oncology, cardiology, neurology, women's health, pain management, gastroenterology and transplantation, helping providers use genetic information to tailor therapy, reduce preventable harm and support more personalized care.
The test is available to clinicians through Labcorp. For more information, visithttps://www.labcorp.com/tests/512275/dpyd-genotyping
About LabcorpLabcorp (NYSE:LH) is a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions. We provide insights and advance science to improve health and improve lives through our unparalleled diagnostics and drug development laboratory capabilities. The company's nearly 71,000 employees serve clients in approximately 100 countries, provided support for more than 85% of the new drugs and therapeutic products approved by the FDA in 2025 and performed more than 750 million tests for patients around the world. Learn more atwww.labcorp.com.

Frequently Asked Questions

What is the purpose of the expanded DPYD test?

The expanded DPYD test identifies cancer patients at risk for severe side effects from fluoropyrimidine chemotherapy.

Which variants does the DPYD test detect?

The test detects all DPYD Tier 1 and Tier 2 variants recommended by the Association for Molecular Pathology.

What are the risks associated with fluoropyrimidine chemotherapy?

Patients with certain DPYD variants may experience severe toxicity, including life-threatening side effects.

How does the DPYD test improve cancer treatment?

It supports safer, personalized cancer care by identifying patients who may not metabolize chemotherapy effectively.

Last updated: May 28, 2026