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在线翻译:
szdaily -> Health -> 
US FDA approves AI pathology program 
    2021-11-25  08:53    Shenzhen Daily

THE U.S. Food and Drug Administration (FDA) has authorized marketing of artificial intelligence (AI) software to help pathologists detect prostate cancer.

The program, called Paige Prostate, is the first approved AI system in pathology.

“We really believe this product can make a huge difference,” Paige CEO Leo Grady, told Medscape Medical News.

The program was approved as an adjunct to pathologist review, not a replacement.

Grady explained that “for a second opinion today, you ship a glass slide to somebody else or you do another stain that’s really expensive or you do another molecular test.”

With Paige Prostate, pathologists digitally scan and upload biopsy slides to their computer, then import them into the program, which is a cloud-based service accessed through a Web browser.

The software compares the tissue patterns against a large database of tissue patterns collected at the Memorial Sloan Kettering Cancer Center, which spun out Paige as a company in 2018 from its work on digitizing and applying AI to pathology slides.

The program looks for patterns that have been previously diagnosed as cancer. When it finds such patterns, it highlights them for the pathologists to key in on, so they “don’t miss anything” and have “a lot more confidence in their diagnosis without having to send it out for additional consultation,” Grady said.

The FDA approval was based on a study in which 16 pathologists examined 527 digitally scanned prostate biopsy slides; 171 of the specimens were cancerous, and 356 were benign. The pathologist made two assessments, one with and one without the program’s help.

The software improved detection of cancer on individual slide images by 7.3 percent on average in comparison with unassisted reads. There was no impact on the read of benign slides.

The FDA said that the risk for false negatives and false positives with the program is mitigated by its use as an adjunct and by pathologists’ consideration of patient history, additional laboratory studies, and other clinical information.

(SD-Agencies)

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