GPSai: A Clinically Validated AI Tool for Tissue of Origin Prediction During Routine Tumor Profiling.

Journal: Cancer research communications
Published Date:

Abstract

A subset of cancers presents with unclear or potentially incorrect primary histopathologic diagnoses, including cancers of unknown primary (CUP). We aimed to develop and validate an artificial intelligence (AI) tool, GPSai, that predicts tumor tissue of origin in CUP and flags potential misdiagnoses for additional workup during routine molecular testing. The GPSai model was trained on whole exome and whole transcriptome data from 201,612 cases submitted for tumor profiling at Caris Life Sciences. Retrospective (N=21,549) and prospective (N=76,271) validations were performed. The clinical impact was evaluated over eight months of live testing and through physician surveys. GPSai demonstrated 95.0% accuracy in non-CUP cases and reported on tumor tissue of origin in 84.0% of CUP and 96.3% of non-CUP cases. During the initial eight months of implementation, GPSai changed the diagnosis on 704 patients (0.88% of all profiled cases), which were supported by orthogonal evidence including imaging, immunohistochemistry, mutational signatures, hallmark fusions, or viral reads. Diagnosis changes prompted changes in targeted-therapy eligibility based on Level 1 clinical evidence in 86.1% of cases (n=606/704). A majority (89.7%; n=87/97) of physician responses indicated acceptance of the GPSai results and 53.6% (n=52/97) of responses stated that the results prompted a change in treatment plan. GPSai accurately identifies tumor tissue of origin and has the potential for clinical impact in a small but meaningful subset of patients with CUP or pathologically ambiguous tumors. Our results support the integration of this AI tool into routine molecular testing to improve diagnostic accuracy and guide subsequent therapeutic decisions.

Authors

  • Hassan Ghani
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Anthony Helmstetter
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Jennifer R Ribeiro
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Todd Maney
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Stephanie Rock
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Rebecca A Feldman
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Jeff Swensen
    Caris Life Sciences (United States), United States.
  • Farah Abdulla
    Caris Life Sciences (United States), United States.
  • David B Spetzler
    Caris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA. dspetzler@carisls.com.
  • Elena Florento
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Ari M Vanderwalde
    West Cancer Center and Research Institute, Germantown, TN, United States.
  • Patricia Pittman
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Milan Radovich
    Caris Life Sciences (United States), Irving, TX, United States.
  • Jaclyn Hechtman
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Casey Bales
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • George W Sledge
    Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Myra M George
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • David Bryant
    Caris Life Sciences (United States), Phoenix, AZ, United States.
  • Jim P Abraham
    Caris Life Sciences (United States), Dallas, TX, United States.
  • Matthew J Oberley
    Caris Life Sciences (United States), Phoenix, AZ, United States.

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