Labcorp Expands MRD Testing for Cancer Recurrence Risk
Labcorp (NYSE: LH), a prominent leader in laboratory services, has announced the expansion of its molecular residual disease (MRD) testing portfolio. This initiative aims to enhance the early detection of cancer recurrence, offering critical insights to clinicians. The newly available tests include Labcorp Plasma Detect ID for stage I–III breast cancer and stage I–IIIA non-small cell lung cancer, along with the Labcorp Plasma Detect Genome for stage III colon cancer, now accessible nationwide.
The Importance of MRD Testing in Cancer Management
Cancer recurrence poses a significant challenge, with substantial rates reported across various cancer types. Statistics show that:
- Approximately 35% of stage III colon cancer patients experience recurrence post-treatment.
- Between 10% to 40% of patients with stage I–III breast cancer face similar risks.
- A staggering 10% to 55% of patients with stage I–III non-small cell lung cancer also deal with recurrence.
MRD testing plays a crucial role in monitoring cancer recurrence by detecting circulating tumor DNA (ctDNA) in the bloodstream, often months before traditional imaging methods can reveal evidence of relapse.
Advancements in Labcorp's MRD Testing Capabilities
Labcorp's tests, including the Labcorp Plasma Detect ID and Labcorp Plasma Detect Genome, can detect ctDNA at an impressive limit of detection (LOD95) of just 0.005%. This capability leads to earlier detection of cancer recurrence, empowering oncologists to customize surveillance and treatment strategies, all while providing clearer information to patients during critical recovery phases.
Dr. Shakti Ramkissoon, M.D., Ph.D., vice president and medical lead for oncology at Labcorp, stated, "Ongoing monitoring is essential to understand the risk of recurrence for patients who have completed cancer treatment with curative intent." He further emphasized that the expansion of the Labcorp Plasma Detect portfolio equips clinicians with advanced tools to enhance patient care.
Research and Clinical Validation of MRD Testing
Labcorp has also conducted numerous clinical studies that validate the utility of its MRD testing in early disease progression tracking and long-term outcome predictions. Noteworthy peer-reviewed studies have highlighted the application of Labcorp Plasma Detect in patients with diffuse pleural mesothelioma and head and neck cancer. Recent data from the AMP 2025 Annual Meeting further underscores the ongoing development of Labcorp Plasma Detect Genome MRD.
Labcorp's Leadership in Oncological Diagnostics
The expansion of Labcorp's Plasma Detect portfolio reinforces its position in oncology diagnostics, supporting patients through screening, diagnosis, and treatment monitoring. With a comprehensive suite of clinical tests, including liquid biopsy and genomic profiling, Labcorp collaborates with healthcare professionals and biopharma companies to advance precision medicine.
For more information on Labcorp's oncology solutions, visit Labcorp Oncology Solutions.
About Labcorp
Labcorp (NYSE: LH) is a global frontrunner in laboratory services, providing crucial insights that aid doctors, hospitals, and researchers in making informed healthcare decisions. Employing nearly 70,000 individuals across approximately 100 countries, Labcorp supports over 75% of new FDA-approved drugs and performs over 700 million tests annually, contributing to improved health outcomes worldwide. Learn more at Labcorp.
For further inquiries regarding the MRD testing or Labcorp services, consult their official channels.