IceCure Medical Highlights Peer‑Reviewed Publications Reinforcing Cryoablation’s Growing Clinical Role In Breast Cancer Treatment De‑Escalation, Including FDA Authorization Of ProSense, Updated ASBrS Guidelines, And Positive ICE3 5‑Yr Outcomes
BBenzingaBenzinga Newsdesk
New review by leading U.S. experts highlights ProSense® FDA marketing authorization, updated American Society of Breast Surgeons guidelines, and encouraging outcomes from the five-year ICE3 clinical trial while a second
IceCure Medical has successfully treated the first patient in its ChoICE post-marketing study, which evaluates the ProSense cryoablation system for treating low-risk breast cancer.
IceCure Medical has officially begun patient enrollment for its post-market clinical study of the ProSense cryoablation system for breast cancer at two U.S. sites.
Featured presentations included 12-month clinical data reporting objective response rates of 97.5% among 40 patients treated with cryoablation plus endocrine therapy and 91.7% among 24 patients treated with cryoablation