News | Prostate Cancer | February 10, 2025

Heatmap uncovers 13% missed cancer rate.


Feb. 10, 2025 —Ibex Medical Analytics recently announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for Ibex Prostate Detect, an in vitro diagnostic medical device that harnesses AI to generate heatmaps identifying small and rare missed prostatic cancers, acting as a safety net to assist pathologists in ensuring patients receive an accurate diagnosis. 

"Prostate cancer is one of the most prevalent cancers worldwide, with an estimated one in eight men diagnosed in their lifetime. With the global incidence expected to double by 2040, accurate and timely diagnoses are more critical than ever. Advancements in AI-powered pathology can support pathologists in delivering precise and efficient diagnoses, ultimately improving patient outcomes,” shared Ibex scientific advisor Mahul B. Amin, MD, Vice President and Medical Director of Labcorp’s Hospital Systems Operating Division and Clinical Professor of Pathology and Laboratory Medicine at the University of Tennessee Health Science Center.

Ibex Prostate Detect is a software-only device that analyzes scanned histopathology whole slide images (WSIs) from prostate core needle biopsies prepared from hematoxylin & eosin (H&E) stained formalin-fixed paraffin embedded tissue. The device is intended to identify tumors that may have been missed by the pathologist. If tissue suspicious for prostate cancer is identified, the system provides case- and slide-level alerts, and includes a heatmap directing the pathologist to areas likely to contain cancer.

In robust precision and clinical validation studies conducted at multiple US and European laboratories as part of the FDA clearance, the system demonstrated a 99.6% positive predictive value (PPV) for cancer heatmap accuracy, and identified a 13% rate of missed cancers in a cohort of consecutive patients initially diagnosed as benign. These missed cancer cases (false negatives) were subsequently verified by expert pathologists, confirming the product’s clinical utility and benefits compared with the current standard of care.1

“The FDA clearance marks a significant milestone in Ibex’s journey and exemplifies our dedication to developing clinically validated solutions that help improve patient health outcomes,” said Joseph Mossel, Chief Executive Officer at Ibex Medical Analytics. “This clearance affirms our commitment to the safety and efficacy of our AI solutions and strengthens our ability to provide cutting-edge innovation to pathologists, which ultimately benefit patients. We hope this accomplishment will bolster industry-wide confidence that AI-powered digital pathology is ready for widespread clinical adoption.”

As cancer incidence rises worldwide, increasing demand and diagnostic workloads are compounded by a global shortage of pathologists, whose jobs are becoming more complex with advancements in precision medicine. Ibex’s platform helps overcome these challenges by empowering pathologists with AI tools that enhance accuracy2-4 and streamline workflows to ensure that every patient receives an accurate and timely diagnosis, which is instrumental both in guiding treatment decisions and improving survival rates of patients with cancer.

Deployed globally in routine clinical use, the Ibex platform includes prostate, breast and gastric solutions that provide pathologists with robust AI-powered tools to support detection of cancer and other clinically relevant findings and improve case review workflows. The platform includes solutions that are CE-IVD certified (per IVDR framework) and registered with the UK MHRA, TGA in Australia and ANVISA in Brazil. Ibex Prostate Detect is FDA cleared and other solutions are Research Use Only (RUO) in the United States. Ibex's quality and security certifications include HITRUST, Cyber Essentials Plus, ISO 27001 and ISO 13485, among others.

For more information about the Ibex platform, please visit: https://ibex-ai.com.

 

1. Ibex precision and clinical validation studies submitted to the FDA (unpublished).

2. Pantanowitz et al. Lancet Digital Health (2020) 2(8): e407-e416.

3. Santa-Rosario et al. Journal of Pathology Informatics (2024), 15:100378.

4. Lami et al. Pathology (2024), 56; 5:633-642

 

 Ibex Prostate Detect is formerly known in the US as Galen Second Read.

 

 


Related Content

News | Mammography

Nov. 26, 2025 — GE HealthCare has announced it received FDA Premarket Authorization for Pristina Recon DL, an advanced ...

Time November 29, 2025
arrow
News | Ultrasound Imaging

Nov 20, 2025 - EDAP TMS SA has announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance ...

Time November 21, 2025
arrow
News | Radiation Therapy

Nov. 11, 2025 — ZAP Surgical Systems recently announced its ZAP-Axon Radiosurgery Planning System has received both U.S ...

Time November 14, 2025
arrow
News | Orthopedic Imaging

Nov.10, 2025 — Medical imaging technology company Adaptix Ltd. has received 510(k) clearance from the U.S. Food and Drug ...

Time November 11, 2025
arrow
News | Cardiac Imaging

Oct. 24, 2025 —YorLabs, Inc., a medical technology company developing next-generation intracardiac imaging solutions for ...

Time October 27, 2025
arrow
News | Computed Tomography (CT)

Oct. 9, 2025 — Harrison.ai has received three FDA Breakthrough Device Designations for CT imaging solutions, further ...

Time October 21, 2025
arrow
News | Women's Health

Oct. 3, 2025 — IceCure Medical Ltd., developer of minimally-invasive cryoablation technology that destroys tumors by ...

Time October 06, 2025
arrow
News | Radiopharmaceuticals and Tracers

Oct. 01, 2025 – Nuclidium AG, a clinical-stage radiopharmaceutical company developing a proprietary copper-based ...

Time October 02, 2025
arrow
News | Magnetic Resonance Imaging (MRI)

Aug. 29, 2025 - Cerebriu recently announced it had received the CE mark for its Apollo Smart Protocol as an OEM-embedded ...

Time September 19, 2025
arrow
News | Proton Therapy

Sept. 15, 2025 — Mevion Medical Systems announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) ...

Time September 18, 2025
arrow
Subscribe Now