Illumina launches advanced liquid biopsy assay to enable comprehensive genomic profiling of solid tumors

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Illumina Inc. has announced the TruSight Oncology 500 ctDNA v2 (TSO 500 ctDNA v2), a new generation of its distributed liquid biopsy assay for genomic profiling. The TSO 500 ctDNA v2 offers faster turnaround time, greater analytical sensitivity, and a more streamlined workflow. Key improvements include a sample-to-answer turnaround time of less than four days, higher sensitivity with lower cell-free DNA input requirements, and automation capabilities in 2024. The assay aims to enable noninvasive comprehensive genomic profiling of circulating tumor DNA to complement tissue-based testing.

TSO 500 ctDNA Version 2 delivers faster turnaround time, greater analytical sensitivity, more streamlined workflow, further enabling precision medicine.

SAN DIEGO, Nov. 1, 2023 /PRNewswire/ -- Illumina Inc. (NASDAQ: ILMN), a global leader in DNA sequencing and array-based technologies, today announced a new generation of its distributed liquid biopsy assay for genomic profiling. The new TruSight™ Oncology 500 ctDNA v2 (TSO 500 ctDNA v2) is a research assay that enables noninvasive comprehensive genomic profiling (CGP) of circulating tumor DNA (ctDNA) from blood when tissue testing is not available, or to complement tissue-based testing.

Key improvements include a faster sample-to-answer turnaround time of less than four days, higher sensitivity with lower cell-free DNA (cfDNA) input requirements, and a more streamlined workflow, which will be further enabled with automation in the first half of 2024.

"Leading cancer centers are increasingly adopting the use of liquid-biopsy-based CGP, and with the TSO 500 ctDNA v2 assay we've aimed to make it easier for customers to integrate and enable deeper insights for cancer research," said Kevin Keegan, general manager of Oncology at Illumina.

Key improvements

• Total turnaround time decreased to less than four days. Library preparation has been reduced to a single day, with improved chemistry requiring a single hybridization step, driving total turnaround time down to less than four days. Most ctDNA CGP assays have a turnaround time of one week or more, but in order for biomarker results to be the most valuable, users need insights sooner to better inform precision oncology efforts.
• More analytically sensitive assay with decreased input amounts. The assay enables analysis from as little as 5 to 30 nanograms (ng) of cfDNA input. At 20 ng input, it shows more than 95% analytical sensitivity with 99.9995% specificity. At 10 ng input, it shows more than 95% sensitivity for hot-spot mutations with 99.9995% specificity. Improved performance can be attributed to both innovations in chemistry and the advanced variant analysis powered by DRAGEN.
• Flexible, streamlined, complete solution. The assay offers broader access to a sample-to-answer distributed solution in both manual and, coming in 2024, automated formats. Workflow improvements reduce hands-on time for library preparation, and automated bioinformatics features further streamline the experience. The assay provides additional flexibility with sequencing compatibility on the NovaSeq 6000 (NovaSeq 6000Dx in research mode and NovaSeq X coming in 2024), as well as local and cloud-based bioinformatics options accommodating the range of institutional preferences.

Nine institutions are participating in Illumina's global early-access customer program to trial TSO 500 ctDNA v2. Giancarlo Pruneri, professor of Pathology at the University of Milan School of Medicine and chair of the Department of Pathology and Laboratory Medicine at the National Cancer Institute of Milan, noted that preliminary testing of the new version of the TSO500 ctDNA panel in their labs "undoubtedly represented an improvement over the previous version."

"In particular, the optimization of library preparation protocol saves one working day, thus enabling a faster delivery of the molecular analysis," he said, "while the increased assay sensitivity allows the analysis of samples with reduced DNA content (20 ng), potentially broadening the utility of liquid biopsy testing."

Growing evidence on the utility and efficacy of liquid biopsy CGP is leading to its inclusion in recommended professional guidelines in oncology. Most notably, liquid biopsy testing in non-small-cell lung cancer has proven useful when tissue results are either unavailable or delayed. This trend is expected to continue for other solid tumor malignancies, which supports the consideration of broad tumor profiling from cfDNA from blood even before tissue analysis.

"Traditional tissue-based analyses are frequently still limited by tissue availability, often involving costly and invasive biopsy procedures," Pruneri said. "In this context, Illumina's new panel emerges as a solution to address the dependency on tissue availability."

Expected in the first half of 2024, automation-enabled kits and method for TSO 500 ctDNA v2 will allow laboratories to scale with the growing demand for this technology.

About TruSight Oncology 500 ctDNA v2
TSO 500 ctDNA v2 is a research-use-only comprehensive pan-cancer assay designed to identify 523 known and emerging tumor biomarkers from blood plasma. TSO 500 ctDNA v2 uses cfDNA from liquid biopsy samples to identify key variants critical for cancer development and progression, such as small DNA variants (SVs), copy number variants (CNVs), short and long insertions and deletions (indels), and immuno-oncology gene signatures like tumor mutational burden (bTMB) and microsatellite instability (bMSI). The content and design of this comprehensive liquid biopsy genomic profiling assay are similar to the tissue-based assay TSO 500, offering a portfolio of solutions. Advanced bioinformatics powered by DRAGEN contribute to the performance and flexiblity of the TSO 500 ctDNA v2 solution. To learn more about TSO 500 ctDNA v2, click here.

Use of forward-looking statements
This release contains forward-looking statements that involve risks and uncertainties, including the expectation for lower costs related to the storing and managing of genomic data costs. Among the important factors that could cause actual results to differ materially from those in any forward-looking statements are: (i) challenges inherent in developing and launching new products and services, including meeting manufacturing, quality, and performance requirements; (ii) our ability to deploy new products, services, and applications, and to expand the markets for our technology platforms; and (iii) the acceptance by customers of our newly launched products, which may or may not meet our and their expectations once deployed, together with other factors detailed in our filings with the Securities and Exchange Commission, including our most recent filings on Forms 10-K and 10-Q, or in information disclosed in public conference calls, the date and time of which are released beforehand. We undertake no obligation, and do not intend, to update these forward-looking statements, to review or confirm analysts' expectations, or to provide interim reports or updates on the progress of the current quarter.

About Illumina
Illumina is improving human health by unlocking the power of the genome. In 2023 we celebrate 25 years of innovation, which has established us as a global leader in DNA sequencing and array-based technologies, serving customers in the research, clinical, and applied markets. Our products are used for applications in the life sciences, oncology, reproductive health, agriculture, and other emerging segments. To learn more, visit illumina.com and connect with us on X (Twitter), Facebook, LinkedIn, Instagram, TikTok, and YouTube.

Contacts

Investors:
Salli Schwartz
858-291-6421
IR@illumina.com

Media:
David McAlpine
347-327-1336
PR@illumina.com

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SOURCE Illumina, Inc.

FAQ

What is the new assay announced by Illumina?

Illumina has announced the TruSight Oncology 500 ctDNA v2 (TSO 500 ctDNA v2), a new generation of its distributed liquid biopsy assay for genomic profiling.

What are the key improvements of the TSO 500 ctDNA v2?

The key improvements of the TSO 500 ctDNA v2 include a sample-to-answer turnaround time of less than four days, higher sensitivity with lower cell-free DNA input requirements, and a more streamlined workflow.

What is the purpose of the TSO 500 ctDNA v2 assay?

The TSO 500 ctDNA v2 assay aims to enable noninvasive comprehensive genomic profiling of circulating tumor DNA to complement tissue-based testing.

When will automation capabilities be available for the TSO 500 ctDNA v2?

Automation capabilities for the TSO 500 ctDNA v2 will be available in the first half of 2024.