Ovarian Cancer Test Delivers Outstanding Diagnostic Performance

Posted: 4 December 2024

INOVIQ Limited (ASX:IIQ or INOVIQ) is pleased to announce that its blood test for ovarian cancer screening has successfully completed an independent patient validation of its biomarkers and diagnostic performance, delivering outstanding test results with accuracy of over 94%. The EXO-OC blood test was performed using a more sensitive and specific method than used in routine pathology testing laboratories.

These results represent a major advancement in OC testing. In this study, exosomes were isolated from more than 500 blood samples, using INOVIQ’s EXO-NET® on a fully-automated high-throughput robotic platform. Exosome ovarian cancer biomarkers, previously identified in the OC97 study, were measured using targeted mass spectrometry performed by The University of Queensland’s (UQ) Centre for Extracellular Vesicle Nanomedicine. All targeted biomarkers were identified in ovarian cancer samples and their diagnostic performance was confirmed using ROC curve analysis and multivariate modelling. EXO-NET isolation of exosomes also identified additional cancer biomarkers for use in the future.

INOVIQ will now move to optimize the blood test on a commercial instrument platform and perform additional clinical validation as a precursor to delivering the test in a clinical laboratory.

The Director of the UQ Centre for Extracellular Vesicle Nanomedicine, Professor Carlos Salomon Gallo, said: “This study demonstrated that the EXO-OC test identified ovarian cancer across all stages with an overall accuracy of over 94%. Notably, the EXO-OC test is particularly accurate in identifying early stages of ovarian cancer, achieving a sensitivity of more than 90% and specificity of 96% for stage I, where women have a 5-year survival rate of over 90%. Importantly, these results confirm that the ovarian cancer biomarkers were validated in an independent sample set, highlighting the robustness and reproducibility of INOVIQ’s EXO-NET exosome isolation technology and UQ’s proprietary biomarkers.”

CEO Dr Leearne Hinch said: “This biomarker panel showed exceptional performance in detecting earlystage ovarian cancer, where accurate diagnosis is most critical for improving patient outcomes. Early detection enables timely intervention, which is crucial for increasing survival rates and reducing disease progression.”

Chairman David Williams said: “This study provides clinical evidence to pursue a commercial product for early ovarian cancer detection.”

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