SOPHiA GENETICS Launches Comprehensive MRD Tracking Capabilities

Rhea-AI Summary

SOPHiA GENETICS (SOPH) has launched the OncoPortal™ Mutation Tracker, a new longitudinal MRD tracking tool for oncology disease monitoring. This add-on module for the SOPHiA DDM™ Platform enables tracking of genomic variants across multiple time points in cancer patients.

The tool combines longitudinal tracking capabilities with next-generation sequencing (NGS) to detect cancer-specific genetic mutations at very low frequencies. Key features include flexible low frequency variant selection, customizable threshold settings, and reporting features that generate longitudinal graphical representations.

According to Dr. Philippe Menu, Chief Medical Officer, the ability to track low frequency variants longitudinally is revolutionary as it enables detection of minimal cancer traces that might escape traditional testing methods. Dr. Christophe Marzac from Gustave Roussy Institute praised the interface as a important solution for broader NGS adoption among oncologists.

Positive

• Launch of innovative OncoPortal™ Mutation Tracker enhances company's oncology monitoring capabilities
• Integration with existing SOPHiA DDM™ Platform expands product ecosystem
• Technology enables early detection of cancer variants that traditional methods might miss

Negative

• None.

Insights

Medical Technology Analyst

The launch of OncoPortal™ Mutation Tracker represents a strategic market expansion in the rapidly growing precision oncology sector, estimated at $49.9 billion globally. This product launch significantly strengthens SOPHiA GENETICS' competitive position in two critical ways:

First, the technology addresses a important market need by enabling high-sensitivity detection of residual cancer cells, potentially capturing a share of the MRD testing market projected to reach $3.88 billion by 2027. The platform's ability to detect low-frequency variants positions it favorably against existing solutions, particularly in monitoring treatment resistance and disease progression.

Second, the endorsement from Gustave Roussy Institute, one of Europe's leading cancer centers, signals strong clinical validation and potential for widespread adoption. The platform's integration with NGS workflows and customizable features addresses key operational inefficiencies in clinical settings, potentially accelerating market penetration.

From a revenue perspective, this launch could drive growth through:

• Increased adoption of SOPHiA's DDM™ Platform
• Recurring revenue from longitudinal patient monitoring
• Cross-selling opportunities within existing customer base
• Expansion into new clinical research centers

The timing is particularly strategic as healthcare systems increasingly prioritize precision medicine approaches, potentially accelerating the product's market acceptance and revenue generation potential.

The cutting-edge OncoPortal™ Mutation Tracker add-on module enables precision monitoring of evolving genomic cancer drivers

BOSTON, MA and ROLLE, Switzerland, Jan. 28, 2025 /PRNewswire/ -- SOPHiA GENETICS (Nasdaq: SOPH), a cloud-native healthcare technology company and a global leader in data-driven medicine, has unveiled the OncoPortal™ Mutation Tracker — a longitudinal MRD tracking tool designed for disease monitoring in the context of oncology. This innovation underscores SOPHiA GENETICS' commitment to advancing data-driven approaches for improved oncology insights.

Tracking genomic variants across multiple time points in the same patient is becoming increasingly critical in cancer care, particularly for identifying treatment resistance or detecting residual cancer cells, such as in Measurable Residual Disease (MRD) management. The integration of longitudinal tracking capabilities with next-generation sequencing (NGS) allow the parallel detection of cancer-specific genetic mutations at very low frequencies. This combined approach enables early identification of residual disease or emerging variants, providing a more precise assessment of disease burden, better stratification of high-risk patients, and the ability to tailor treatments to the cancer's unique genomic profile.

The OncoPortal™ Mutation Tracker augments the SOPHiA DDM™ Platform's core analytical capabilities to allow clinical researchers to longitudinally monitor evolving genomic variants across multiple time points, providing a comprehensive view of disease evolution. The OncoPortal™ Mutation Tracker enhances workflow efficiency for longitudinal variant tracking by offering flexible low frequency variant selection, customizable threshold settings, and reporting features to generate longitudinal graphical representations, simplifying the process of tracking and analyzing genetic changes over time.

"The ability to reliably track low frequency variants longitudinally is a game-changer because it allows the detection of even the smallest traces of cancer that can evade traditional methods of testing and ultimately drive relapse," said Philippe Menu, M.D., Ph.D., Chief Medical Officer and Chief Product Officer, SOPHiA GENETICS. "With this new longitudinal tracking capability, we offer a highly customizable, user-friendly solution to enable the generation of novel insights for clinical research. Precise tracking of key genomic variants over time has the potential to eventually enable earlier intervention and more tailored disease management, which may lead to better long-term outcomes for patients."

"This longitudinal interface represents the solution we've been seeking to unite our oncologists in embracing broader adoption of NGS. It's the missing piece that unlocks a new frontier in personalized, data-driven medicine," said Dr. Christophe Marzac, Head of the Hematology-Immunology Unit, Gustave Roussy Institute.

For more information on the OncoPortal™ Mutation Tracker, visit SOPHiAGENETICS.com.

About SOPHiA GENETICS 

SOPHiA GENETICS (Nasdaq: SOPH) is a cloud-native healthcare technology company on a mission to transform patient care by expanding access to data-driven medicine globally. It is the creator of the SOPHiA DDM™ Platform, which analyzes complex genomic and multimodal data and generates real-time, actionable insights for a broad global network of hospital, laboratory, and biopharma institutions. For more information, visit SOPHiAGENETICS.com and connect with us on LinkedIn.

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise. The information in this press release is about products that may or may not be available in different countries and, if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact support@sophiagenetics.com to obtain the appropriate product information for your country of residence. 

SOPHiA GENETICS Forward-Looking Statements:

This press release contains statements that constitute forward-looking statements. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations and financial position, business strategy, products, and technology, as well as plans and objectives of management for future operations, are forward-looking statements. Forward-looking statements are based on our management's beliefs and assumptions and on information currently available to our management. Such statements are subject to risks and uncertainties, and actual results may differ materially from those expressed or implied in the forward-looking statements due to various factors, including those described in our filings with the U.S. Securities and Exchange Commission. No assurance can be given that such future results will be achieved. Such forward-looking statements contained in this press release speak only as of the date hereof. We expressly disclaim any obligation or undertaking to update these forward-looking statements contained in this press release to reflect any change in our expectations or any change in events, conditions, or circumstances on which such statements are based, unless required to do so by applicable law. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements. 

View original content to download multimedia:https://www.prnewswire.com/news-releases/sophia-genetics-launches-comprehensive-mrd-tracking-capabilities-302362038.html

SOURCE SOPHiA GENETICS

FAQ

What is the OncoPortal™ Mutation Tracker launched by SOPHiA GENETICS (SOPH)?

The OncoPortal™ Mutation Tracker is a longitudinal MRD tracking tool that enables monitoring of evolving genomic cancer drivers, allowing detection of cancer-specific genetic mutations at very low frequencies across multiple time points.

How does SOPHiA GENETICS' new mutation tracker improve cancer monitoring?

It improves cancer monitoring by enabling early identification of residual disease, better stratification of high-risk patients, and detection of emerging variants, potentially leading to more precise disease assessment and tailored treatments.

What are the key features of SOPH's OncoPortal™ Mutation Tracker?

Key features include flexible low frequency variant selection, customizable threshold settings, and reporting features that generate longitudinal graphical representations of genetic changes over time.

How does the OncoPortal™ Mutation Tracker integrate with SOPHiA GENETICS' existing platform?

It integrates as an add-on module to the SOPHiA DDM™ Platform, augmenting its core analytical capabilities to allow clinical researchers to monitor genomic variants across multiple time points.