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    WHO-Aligned Molecular Classification

    One Test. One Snapshot.
    Complete Clarity.

    The first integrated molecular profiling assay for endometrial cancer—delivering biology-driven
    treatment decisions from a single tissue sample.

    2,000 ×

    Sequencing Depth

    12-14 Days

    Turnaround Time

    6

    Molecular Sub types

    The Challenge

    Fragmented Testing.
    Fragmented Decisions.

    Current workflows are sequential, slow, and tissue-intensive—leading to 
    delays and missed treatment opportunities.

    Prolonged Turnaround

    Molecular tests ordered sequentially across multiple labs. Results arrive at different times, delaying critical treatment decisions.

    Over & Under Treatment

    Without complete molecular context, POLE-mutated patients face unnecessary chemo while TP53-abnormal cases may be undertreated.

    Tissue Exhaustion

    Repeated testing consumes precious tissue—especially in small biopsies—leaving nothing for additional analyses when most needed.

    Missed Therapies

    Incomplete molecular profiling means patients may miss eligibility for immunotherapy, targeted therapy, or hormone therapy entirely.

    "Endometrial cancer care can no longer afford fragmented diagnostics."

    The Solution

    A Single, Integrated Molecular Snapshot

    OncoIndx 360° Endometrium replaces fragmented workflows with one comprehensive, biology-driven report that links molecular subtype to prognosis and treatment strategy.

    Testing

    Upfront, Integrated Testing

    NGS + IHC + MSI performed together—not sequentially. Eliminates TAT delays and tissue exhaustion from the start.

    Report

    Single Molecular Snapshot

    One sample. One test. One report. No compromises. Aligned with ESGO/ESTRO/ESP guidance for early molecular classification.

    Biology

    Biology That Drives Decisions

    Molecular subtypes are not just reported—they are interpreted and translated into actionable treatment pathways for each patient.

    Innovation

    NSMP, Finally Actionable

    ER-stratified NSMP classification transforms a “leftover category” into biologically meaningful, clinically actionable information.

    Guidelines

    Guidelines, Made Practical

    Fully operationalizes ESGO/ESTRO/ESP and WHO molecular classification recommendations in real-world clinical practice.

    Head-to-Head

    Today's Pathway vs. OncoIndx® 360°

    Parameter Today's Pathway OncoIndx® 360°
    Testing Approach Sequential, fragmented, across multiple labs Upfront, integrated, single tissue sample
    Molecular Coverage Limited, often incomplete Complete (NGS + IHC + MSI)
    Turnaround Time Prolonged & unpredictable Predictable: 10–14 Days
    Tissue Usage High – risk of exhaustion Tissue-sparing — one sample for all
    NSMP Interpretation Ambiguous "diagnosis of exclusion" Actionable, ER-stratified biology
    Treatment Decisions Variable, morphology-driven Consistent, WHO-aligned, biology-driven

    WHO-Aligned Classification

    Molecular Subtypes, Clinically Decoded

    OncoIndx 360° evaluates all WHO-relevant molecular layers and classifies tumors into clinically actionable categories with clear prognosis and treatment implications.

    Excellent Prognosis

    POLE-ultramutated

    Safe treatment de-escalation; avoid unnecessary chemotherapy even when histologically high-grade.

    Intermediate / Therapy-Responsive

    MMRd / MSI-High

    Prioritize immunotherapy, with significant benefit expected from checkpoint inhibitor-based treatment regimens.

    Poor Prognosis

    TP53-abnormal

    Treatment escalation required. Intensive chemotherapy ± HER2-targeted therapy for aggressive biology.

    Favorable-Intermediate

    NSMP — ER Positive

    Hormone-based therapy with reduced cytotoxic exposure. Biologically distinct with better recurrence profile.

    Intermediate-Poor

    NSMP — ER Negative

    Standard cytotoxic therapy with closer surveillance. Distinct risk profile from ER-positive NSMP.

    Poor → Improved with Targeted Rx

    HER2-positive

    Precision escalation with HER2-targeted agents. Prognosis significantly improves with appropriate targeted therapy.

    NSMP is no longer a "leftover category" — it is biologically stratified and clinically interpreted, driving real post-surgical decisions.

    Get Started

    Ready to Transform Cancer
    Diagnostics?

    Designed for oncologists managing complex, advanced and refractory cancer patients. Get more information about OncoIndx360 for your clinical setting.

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      Fill in your details to explore real-world oncology insights…


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