PAIP 2023 Challenge Winner and MICCAI 2022 ACROBAT Challenge Winner
April 21, 2023 –Spokane, WA. Gestalt Diagnostics is honored to have taken 1st place in both International challenges. Hundreds of groups participated in each challenge and Gestalt’s algorithms achieved highest ranking.
In September 2022, Gestalt was awarded 1st place in MICCAI’s Automatic Registration of Breast Cancer Tissue Challenge.
Hundreds of groups participated in each challenge and Gestalt’s algorithms achieved highest ranking.
On April 18th, 2023, Gestalt was named the 1st place winner in the PAIP’s Tumor Cellularity Prediction in Pancreatic Cancer and Colon Cancer Challenge. Gestalt’s algorithm had an ICC score of .9764 with nearly 98% efficacy.
International challenges enable companies such as Gestalt to collaborate with colleagues on their development by competing on items such as theory, application, approach and finally being scored on what matters most, the accuracy of the algorithm when it is applied and scientifically reviewed.
“These challenges are an excellent opportunity to compare and validate the techniques Gestalt uses to develop state-of-the-art image analysis algorithms that support the diagnostic workflow of physicians who utilize our digital pathology platform,” says Brian Napora, Gestalt VP, AI Solutions.
Gestalt Diagnostics, Inc.
Gestalt Diagnostics transforms pathology through an intelligent, configurable, vendor-neutral, and AI-driven digital workflow that provides true interoperability enabling pathologists to diagnose* diseases faster and more efficiently. Our PathFlow® solution consists of professional, education, and research modules for ease of mixing and matching the digital needs of your facility in a single solution, freeing pathologists from tedious, repetitive, and manual tasks allowing them to focus on their expertise, equipping pathologists with key data to provide the best care in the fight against disease, including cancer.
*Research Use Only (RUO) unless following CAP guidelines for LDT. CE-certified per in vitro diagnostic Medical Device Directive 98/79/EEC.
