Clinical Validation

Figure 1. Significant Improvement in Response Prediction to NAC over SOC using the QPOR™ Platform, N=88

The QPOR™ Platform Predicts Neoadjuvant Chemotherapy Response in Multiple Subgroups of Breast Cancer

  • Retrospective analysis of completed Phase II trial with a leading cancer center and national consortium predicting neoadjuvant chemotherapy response in TNBC and HER2-/ER+ breast cancer (N=88)
  • The 4D Path QPOR™ indices (signature) used in this study are predictive of neoadjuvant chemotherapy (NAC) response from the images of pre-treatment H&E biopsies across therapies
  • Significant improvement in response prediction over current evaluation using standard clinic-pathological features (Figure 1)
    • 40% accuracy using current standard of care method
    • >80% using QPOR™ with our default screen and 98% using our customized screen (increase in %Responder >100%)
  • Data presented at ASCO 2024

Figure 2. Cohort selection for immunotherapy benefit by QPOR™ Immune Signature Status, N=81

QPOR™ Platform Predicts Response to Immunotherapy in Patients with Metastatic Melanoma

In a retrospective review of 81 metastatic melanoma patients, who were assigned to receive IO therapy based on PDL1, status:

  • 36 patients received IO and 45 patients did not
  • No statistically meaningful OS was observed (p=0.06).

All patients were stratified using the QPOR™ immune profile, “SVI”, into high and low cohorts,

  • In the high cohort, there was a statistically significant difference in outcomes between those who received IO and those who did not (Figure 2)
  • Furthermore, using the QPOR™ platform to predict IO therapy response demonstrated >50% patients received ineffective or inappropriate treatment because current diagnostic tests are insufficient.
    • Significant immunotherapy benefit for 51% (41/81) patients with median 6+ years of improvement in OS
    • 28% (23/81) patients would benefit from immunotherapy who would otherwise be missed by current SOC