American Society of Breast Surgeons (ASBrS) Resource Guide Update Recommends Cryoablation for Low-Risk Breast Cancer
MWN-AI** Summary
The American Society of Breast Surgeons (ASBrS) has updated its 2026 Resource Guide, now recommending cryoablation as a treatment option for selected patients with biologically low-risk early-stage breast cancer, particularly those aged 70 and above with tumors up to 1.5 cm. This update follows the positive feedback from the FDA Advisory Panel regarding IceCure Medical's ProSense® system and its favorable benefit-risk profile for low-risk breast cancer, which received FDA marketing clearance in October 2025.
Cryoablation is a minimally invasive technique that destroys tumors by freezing them, thus providing a breast-conserving alternative to surgical tumor removal. The updated guidelines highlight the importance of incorporating cryoablation into comprehensive treatment plans, emphasizing multidisciplinary collaboration to ensure the best patient outcomes. As Eyal Shamir, CEO of IceCure, articulated, this endorsement signifies a validation of cryoablation's role in modern breast cancer management while focusing on patient-centered care, cosmetic results, and reduced recovery times.
As cryoablation aligns with broader trends toward preservation and de-escalation in breast cancer treatments, the ASBrS's recognition is anticipated to enhance awareness and confidence in cryoablation among patients and healthcare providers. Additionally, a new CPT III reimbursement code for cryoablation is expected to further facilitate its adoption.
ProSense® has the potential to cater to a significant patient population, with approximately 200,000 women annually in the U.S. eligible for breast cryoablation, including those who are not surgical candidates. With its FDA clearance and emerging clinical guidelines, IceCure is positioned to gain momentum in the breast cancer treatment landscape, providing a safer, effective, and patient-friendly option for tumor management.
MWN-AI** Analysis
The recent update from the American Society of Breast Surgeons (ASBrS) recommending cryoablation as a treatment option for low-risk breast cancer is a significant development for stakeholders in the healthcare sector, particularly investors in bio-pharmaceutical and medical technology companies like IceCure Medical Ltd. (Nasdaq: ICCM). This endorsement enhances the credibility of IceCure's ProSense® cryoablation system, which targets a demographic of approximately 200,000 women annually in the U.S.
The ASBrS’s 2026 Resource Guide officially identifying cryoablation as an appropriate treatment augments the momentum generated by the FDA's marketing clearance for ProSense® last year. Such recognition is critical for boosting adoption rates among breast surgeons and expanding the product's market penetration. Given that the system offers a minimally invasive alternative for patients aged 70 and older, the growing emphasis on individualized patient care, preservation of breast aesthetics, and reduced recovery times aligns well with current healthcare trends.
For potential investors, IceCure’s anticipated commercial adoption driven by this endorsement could present a lucrative opportunity. The existence of a CPT III reimbursement code further increases the likelihood of widespread insurance coverage for procedures utilizing the ProSense® system, thereby enhancing accessibility and fostering revenue growth momentum.
As healthcare stakeholders seek to balance treatment efficacy with patient outcomes, IceCure’s technology appears well-positioned to capitalize on this intersection. However, investors should remain cognizant of potential risks related to regulatory changes, market competition, and the necessity of clinical evidence to sustain this growth trajectory. Implementing a diversified investment strategy while closely monitoring IceCure’s performance and market reception will be vital to maximizing returns in this evolving sector.
**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.
PR Newswire
IceCure's ICE3 study and the FDA Advisory Panel's favorable vote on ProSense® cryoablation's benefit-risk profile for low-risk breast cancer played a key role in the ASBrS 2026 Resource Guide update
New medical society guidance expected to further accelerate commercial adoption of ProSense® following FDA-clearance for low-risk breast cancer in October 2025
CAESAREA, Israel, March 9, 2026 /PRNewswire/ -- IceCure Medical Ltd. (Nasdaq: ICCM) ("IceCure", "IceCure Medical" or the "Company"), a developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an option to surgical tumor removal, today announced that the American Society of Breast Surgeons' ("ASBrS") updated 2026 "Resource Guide on the Use of Transcutaneous and Percutaneous Ablation for the Treatment of Benign and Malignant Tumors of the Breast" recommends cryoablation as an option for selected patients with biologically low-risk early-stage breast cancer. The updated guidance represents an important step toward broader clinical adoption of IceCure's ProSense® cryoablation system, which received U.S. Food and Drug Administration ("FDA") marketing clearance in October 2025 for the treatment of low-risk breast cancer in patients aged ?70 years, with tumors measuring ?1.5 cm, who are treated with adjuvant endocrine therapy. ProSense® is the first and only FDA cleared medical device for the treatment of breast cancer.
"We believe this recognition by the ASBrS, a leading professional society, further validates cryoablation's role in modern breast cancer care and positions ProSense® as an option that prioritizes outcomes, cosmetic results, and patient choice," said Eyal Shamir, IceCure's Chief Executive Officer. "The ASBrS Resource Guide on percutaneous ablation compliments their recent guidance for breast-conserving treatment, emphasizing preservation, de-escalation, and individualized care. Cryoablation aligns naturally with these principles by providing minimally invasive, breast-preserving local tumor control without surgical excision."
IceCure's Vice President of Sales for North America, Shad Good, added, "We believe ASBrS's new guidance will further raise awareness of and confidence in cryoablation among patients and breast surgeons, who develop and oversee breast cancer patients' treatment plans. We expect these developments, as well as the established CPT III reimbursement code, will help further accelerate commercial adoption and drive continued momentum in ProSense® system placements and procedure volumes."
The ASBrS 2026 Resource Guide continues to recognize cryoablation as a validated, cosmetically favorable treatment for benign fibroadenomas and now identifies it as a carefully selected, FDA-approved option to surgery for biologically low-risk early-stage breast cancer in older patients. The guide indicates that cryoablation must be considered in the context of a comprehensive treatment plan with input from a multidisciplinary team. The ASBrS recommendations align clinical evidence, FDA authorization, and multidisciplinary care principles into a unified framework for the use of breast cryoablation.
Based on data from the American Cancer Society, ProSense® addresses a U.S. breast cryoablation patient population of approximately 200,000 women annually, including an estimated 47,245 early-stage, low-risk breast cancer patients aged 70 and over, approximately 90,300 patients who are not candidates for breast cancer surgery, and roughly 63,200 patients with fibroadenomas who opt for excision.
About ProSense®
The ProSense® Cryoablation System is the first and only medical device to receive FDA marketing authorization for the local treatment of low-risk breast cancer with adjuvant endocrine therapy for women aged 70 and above, including patients who are not suitable for surgical alternatives for breast cancer treatment. A full list of benefits and risks can be found on the Company's website.
ProSense® is a minimally invasive cryosurgical tool that provides the option to destroy tumors by freezing them. The system uniquely harnesses the power of liquid nitrogen to create large lethal zones for maximum efficacy in tumor destruction in benign and cancerous lesions, including in the breast, kidney, lung, and liver.
ProSense® enhances patient and provider value by accelerating recovery, reducing pain, surgical risks, and complications. With its easy, transportable design and liquid nitrogen utilization, ProSense® opens the door to fast and convenient office-based procedures for breast tumors.
About IceCure Medical
IceCure Medical (Nasdaq: ICCM) develops and markets advanced liquid-nitrogen-based cryoablation therapy systems for the destruction of tumors (benign and cancerous) by freezing, with the primary focus areas being breast, kidney, bone and lung cancer. Its minimally invasive technology is a safe and effective option to surgical tumor removal that is easily performed in a relatively short procedure. The Company's flagship ProSense® system is marketed and sold worldwide for the indications cleared and approved to date including in the U.S., Europe, and Asia.
Forward Looking Statement
This press release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995 and other Federal securities laws. Words such as "expects," "anticipates," "intends," "plans," "believes," "seeks," "estimates" and similar expressions or variations of such words are intended to identify forward-looking statements. For example, IceCure is using forward looking statements in this press release when it discusses: the expected impact of the of the ASBrS 2026 Resource Guide update on physician adoption, patient access, reimbursement coverage, and commercial adoption of ProSense®; the Company's belief that ProSense® is positioned as a treatment option that prioritizes outcomes, cosmetic results, and patient choice; that the ASBrS guidance is expected to further accelerate commercial adoption of ProSense® following FDA-clearance for low-risk breast cancer in October 2025; and the Company's expectations regarding the role of cryoablation as a minimally invasive treatment option for appropriately selected breast cancer patients. Historical results of scientific research and clinical and preclinical trials do not guarantee that the conclusions of future research or trials will suggest identical or even similar conclusions. Important factors that could cause actual results, developments and business decisions to differ materially from those anticipated in these forward-looking statements include, among others: the Company's planned level of revenues and capital expenditures; the Company's available cash and its ability to obtain additional funding; the Company's ability to market and sell its products; legal and regulatory developments in the United States and other countries; the Company's ability to maintain its relationships with suppliers, distributors and other partners; the Company's ability to maintain or protect the validity of its patents and other intellectual property; the Company's ability to expose and educate medical professionals about its products; political, economic and military instability in the Middle East, specifically in Israel; as well as those factors set forth in the Risk Factors section of the Company's Annual Report on Form 20-F for the year ended December 31, 2024 filed with the SEC on March 27, 2025, and other documents filed with or furnished to the SEC which are available on the SEC's website, www.sec.gov. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.
IR Contact:
Email: investors@icecure-medical.com
Michael Polyviou
Phone: 732-232-6914
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SOURCE IceCure Medical
FAQ**
How does the ASBrS 2026 Resource Guide update, which recommends cryoablation for low-risk breast cancer, impact the market potential for IceCure Medical Ltd. ICCM's ProSense® system in the coming years?
What clinical evidence supports the ASBrS's recommendation for cryoablation in low-risk breast cancer patients, and how does IceCure Medical Ltd. ICCM plan to leverage this in their marketing strategy?
With the approval of ProSense® cryoablation for treating low-risk breast cancer, what role does IceCure Medical Ltd. ICCM foresee for this technology in conjunction with adjuvant endocrine therapy among older patients?
In light of the ASBrS's updated guidance, how is IceCure Medical Ltd. ICCM planning to address potential concerns regarding the efficacy and safety of cryoablation among breast cancer specialists and patients?
**MWN-AI FAQ is based on asking OpenAI questions about IceCure Medical Ltd. (NASDAQ: ICCM).
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