PALO ALTO, CALIF.--(BUSINESS WIRE)--
Lucence, a precision oncology company using liquid biopsy to bring clarity to cancer care, is announcing the availability of an expanded version of its flagship LiquidHALLMARK liquid biopsy assay that includes both cell-free DNA (cfDNA) and cell-free RNA (cfRNA) profiling. LiquidHALLMARK cfDNA and cfRNA is currently available to US oncologists as a laboratory developed test and is being utilized by physicians at NCI-designated centers across the country.
Most liquid biopsies available today interrogate cell-free DNA (cfDNA) as the sole analyte. However, for the detection of certain fusions, including those that have long intronic regions such as NTRK and NRG1, incorporation of RNA sequencing can be advantageous. Gene fusions like NTRK and NRG1 have emerged as clinically significant and actionable biomarkers that can help guide physicians to matched targeted therapies. Ryma Benayed and co-authors demonstrated that adding targeted RNA sequencing to DNA sequencing to tissue testing could obtain an additional 14% yield of clinically actionable alterations.
An internal validation study conducted by Lucence also supports this approach. Out of 112 non-small cell lung cancer (NSCLC) samples, 29 fusions were detected with a combined cfDNA and cfRNA approach in plasma, compared with 20 fusions from cfDNA alone.
“Including cfRNA in a liquid biopsy assay has a significant impact on the detection of clinically relevant fusions. This solves a major known limitation of cfDNA-only assays, which have more limited fusion detection capabilities. For example, NTRK fusions which have corresponding approved TRK inhibitors, and NRG fusions which have multiple emerging therapies, are best detected by a combination of both DNA and RNA testing. This is an exciting opportunity to help more cancer patients through broader and more accurate targeting,” said Professor Gilberto Lopes, Chief of Medical Oncology at Sylvester Cancer Center at the University of Miami.
“Lucence’s experience using AmpliMark for SARS-CoV-2 as part of the fight against the COVID-19 pandemic gave us the experience with RNA to be able to expand our assay to detect fusions in cancer. It’s a great example of how R&D developed to fight COVID can now be used for ultrasensitive cancer diagnostics,” said Dr. Min-Han Tan, MBBS, PhD, Founding CEO and Medical Director of Lucence.
Lucence’s LiquidHALLMARK cfDNA and cfRNA panel combines cfRNA profiling of 27 actionable and emerging fusions with cfDNA profiling of mutations in 80 genes, fusions in 10 genes, and somatic variants in 15 cancer types. LiquidHALLMARK is powered by AmpliMark, the Company’s proprietary amplicon-based sequencing technology, which uses a unique molecular barcode and error-correction technology to ensure test sensitivity across multiple mutation types for single nucleotide variants and fusion genes.
Lucence is a precision oncology company committed to bringing clarity to cancer care. Lucence makes ultrasensitive liquid biopsy tests to provide doctors and their patients life-changing information to enable earlier detection and effective treatment. Headquartered in Palo Alto, Lucence supplies personalized cancer care services through twin CAP-accredited CLIA-licensed laboratories in California and Singapore. For more information, visit www.lucence.com.
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