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Personalizing Treatment for Patients with mHSPC

Leveraging multimodal artificial intelligence (MMAI), the ArteraAI Prostate Test (mHSPC) provides patient-specific risk estimates to help guide treatment intensity and duration decisions for patients with metastatic hormone-sensitive prostate cancer.

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Explore the ArteraAI Prostate Test Report (mHSPC) and how it can help personalize prostate cancer treatment.

ArteraAI Prostate Test Benefits

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Patient-Specific Risk Assessment

The ArteraAI Prostate Test (mHSPC) is the first AI-powered test that provides individualized 5-year PCSM risk estimates for patients with metastatic hormone-sensitive prostate cancer. Results help guide therapy intensity and duration decisions, balancing efficacy and quality of life considerations.

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Fast and convenient

Since the test uses digitized images from the patient's diagnostic prostate biopsy slides and clinical information, test results can be shared within 1-2 days after specimen receipt. There's no tissue consumption or risk of insufficient tissue sample leading to inconclusive results.

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Rigorous Validation

The ArteraAI Prostate Test (mHSPC) was validated in 1,598 patients with metastatic prostate cancer from the STAMPEDE phase III trial. The underlying multimodal artificial intelligence (MMAI) platform has been validated in thousands of patients across multiple clinical trials.

Developed to Guide Treatment Decisions in mHSPC

Medical oncologists treating mHSPC patients face a critical decision: should patients receive doublet therapy (ADT + ARPI) or escalate to triplet therapy with docetaxel? Traditional risk factors like metastatic volume provide broad categories but lack the precision needed to confidently personalize treatment.



The ArteraAI Prostate Test provides a patient-specific 5-year PCSM risk estimate based on doublet hormone therapy (ADT + ARPI). This individualized assessment refines risk stratification beyond volume alone, helping clinicians balance treatment efficacy against the known toxicities of therapy intensification.

Risk Stratification Within Metastatic Volume Subgroups

Risk Group Chart

The ArteraAI Prostate Test provides the patient’s individual MMAI score percentile ranking and 5-year PCSM risk with standard doublet hormone therapy, within metastatic volume subgroups.

 

Two Ways to Order the ArteraAI Prostate Test (mHSPC)

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Order Directly Through Artera (Available Now)

Our team will guide you through account activation and provide all necessary forms and support.

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Risk Group Chart

Order Through Tempus (Available Soon)

For physicians who use Tempus for comprehensive genomic profiling, you will soon be able to add the ArteraAI Prostate Test (mHSPC) to your Tempus xT CDx, xT, or xR orders. Sign up to be notified when this option becomes available.

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Explore Artera resources

Test Guide

This brochure provides an explanation of how the ArteraAI Prostate Test (mHSPC) works, how it was validated, and how it can be used to inform treatment planning for patients with metastatic hormone-sensitive prostate cancer.

Test Requisition Form

The test requisition form can be completed and faxed into Artera to order the ArteraAI Prostate Test for a patient. This form requires an ordering clinician signature.

Sample Test Report

This is a sample test report to show how the ArteraAI Prostate Test (mHSPC) results will appear when testing is completed.

Ordering is Easy with Artera

The ArteraAI Prostate Test is a laboratory-developed testTesting is performed by ArteraAI, located at 6800 Southpoint Pkwy Suite 950, Jacksonville, Florida 32216. The ArteraAI Prostate Test was developed and its performance characteristics were determined by ArteraAI. This Laboratory is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA ‘88) as qualified to perform high-complexity clinical laboratory testing. This test is used for clinical purposes and should not be regarded as investigational or for research. This test has not been cleared or approved by the U.S. Food and Drug Administration. that is now clinically available through a single CLIA-certified laboratory in Jacksonville, FL.

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