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Related Experiment Video

Updated: Jul 28, 2025

Predicting Treatment Response to Image-Guided Therapies Using Machine Learning: An Example for Trans-Arterial Treatment of Hepatocellular Carcinoma
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Xerna™ TME Panel is a machine learning-based transcriptomic biomarker designed to predict therapeutic response in

Mark Uhlik1, Daniel Pointing2, Seema Iyer1

  • 1OncXerna Therapeutics, Inc., Waltham, MA, United States.

Frontiers in Oncology
|May 30, 2023
PubMed
Summary

A novel RNA expression biomarker, the Xerna™ Tumor Microenvironment (TME) Panel, predicts response to diverse cancer therapies. This pan-tumor classifier identifies four TME subtypes, showing broad clinical utility across multiple cancer types and treatment modalities.

Keywords:
anti-angiogenic agentdiagnostic assayimmunotherapypan-tumorpredictive biomarker

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Area of Science:

  • Oncology
  • Biomarker Development
  • Computational Biology

Background:

  • Current predictive biomarkers often focus on single analytes, limiting their clinical utility.
  • There is a need for broad, multi-therapeutic predictive biomarkers.
  • The tumor microenvironment (TME) plays a critical role in therapeutic response.

Purpose of the Study:

  • To develop and validate a novel, pan-tumor RNA expression-based biomarker, the Xerna™ TME Panel.
  • To predict patient response to multiple TME-targeted therapies, including immunotherapies and anti-angiogenic agents.
  • To classify tumors into distinct TME subtypes.

Main Methods:

  • An artificial neural network (ANN) algorithm was trained on a 124-gene signature from 298-patient solid tumor data.
  • The model identified four TME subtypes: Angiogenic (A), Immune Active (IA), Immune Desert (ID), and Immune Suppressed (IS).
  • The classifier's performance was evaluated in four independent clinical cohorts across gastric, ovarian, and melanoma datasets.

Main Results:

  • The TME Panel successfully discriminated four distinct stromal phenotypes based on angiogenesis and immune axes.
  • The classifier demonstrated significant enrichment (1.6-to-7-fold) of clinical benefit across multiple therapeutic hypotheses.
  • The Panel outperformed PD-L1 and MSI-H biomarkers in specific metrics for gastric cancer immunotherapy response prediction.

Conclusions:

  • The Xerna™ TME Panel exhibits strong performance across diverse datasets and therapeutic modalities.
  • The biomarker's ability to predict response to multiple TME-targeted therapies suggests broad clinical utility.
  • The findings support the potential use of the TME Panel as a clinical diagnostic tool for various cancer types.