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Conference Paper: Initial experience on broadening the use of cryoablation on early breast cancer (Oral presentation)

TitleInitial experience on broadening the use of cryoablation on early breast cancer (Oral presentation)
Authors
Issue Date17-Apr-2025
Abstract

Background: The ICE-3 trial final report in 2024 indicated that cryoablation is a feasible treatment for luminal breast cancers (BC) ≤ 1.5 cm. This study aimed to broaden the eligibility criteria for cryoablation to include T1 BC of all IHC subtypes.

Methods: This single-center, single-armed prospective trial assessed cryoablation for early-stage BC. Inclusion criteria included biopsy-confirmed invasive or in-situ BC ≤ 2 cm. Those with lobular carcinomas and tumors < 5 mm from the skin were excluded. Patients underwent contrast MRI and PET-CT scans to confirm eligibility. Cryoablation was performed by the same surgeons using intra-operative ultrasound guidance, with axillary surgery in the same setting if indicated. A 14 mm circumferential ablative margin was adopted. Procedure duration and iceball size were recorded, and patients were regularly followed for pain and complications. Contrast breast MRI, regional PET-CT scans, and core biopsies were conducted six weeks post-cryoablation to assess tumor viability.


Result: Among 53 patients, 33 received cryoablation. Out of the 20 excluded patients, 35% of the patients were excluded due to size discrepancy and 25% were excluded due to multifocal lesions detected from MRI screening. The median age was 64, and median tumor size was 11.95 mm. There were 4 (12.1%) DCIS and 29 (87.8%) invasive cancers, including 1 (3.4%) TNBC. The median procedure time was 52 minutes, with all patients undergoing two freeze-thaw cycles. The median final iceball size was 50.6 mm. The median pain score one week post-ablation was 1 out of 10, with no significant complications reported. 82.6% of patients had follow-up imaging 6-week post-cryosurgery and biopsy. Additionally, 71.4% of the patients had completed 1-year postcryosurgery MRI/PET-CT. All displayed no radiological evidence of residual malignancy.

Conclusions: Cryoablation effectively ablated T1 BC, including TNBC. Further studies are needed to confirm its broader applicability. MRI scan is an essential tool to provide better patient selection


Persistent Identifierhttp://hdl.handle.net/10722/355707

 

DC FieldValueLanguage
dc.contributor.authorKwong, Ava-
dc.contributor.authorCo, Tiong Hong Michael-
dc.date.accessioned2025-05-05T00:35:27Z-
dc.date.available2025-05-05T00:35:27Z-
dc.date.issued2025-04-17-
dc.identifier.urihttp://hdl.handle.net/10722/355707-
dc.description.abstract<p>Background: The ICE-3 trial final report in 2024 indicated that cryoablation is a feasible treatment for luminal breast cancers (BC) ≤ 1.5 cm. This study aimed to broaden the eligibility criteria for cryoablation to include T1 BC of all IHC subtypes.<br></p><p>Methods: This single-center, single-armed prospective trial assessed cryoablation for early-stage BC. Inclusion criteria included biopsy-confirmed invasive or in-situ BC ≤ 2 cm. Those with lobular carcinomas and tumors < 5 mm from the skin were excluded. Patients underwent contrast MRI and PET-CT scans to confirm eligibility. Cryoablation was performed by the same surgeons using intra-operative ultrasound guidance, with axillary surgery in the same setting if indicated. A 14 mm circumferential ablative margin was adopted. Procedure duration and iceball size were recorded, and patients were regularly followed for pain and complications. Contrast breast MRI, regional PET-CT scans, and core biopsies were conducted six weeks post-cryoablation to assess tumor viability.</p><p><br></p><p>Result: Among 53 patients, 33 received cryoablation. Out of the 20 excluded patients, 35% of the patients were excluded due to size discrepancy and 25% were excluded due to multifocal lesions detected from MRI screening. The median age was 64, and median tumor size was 11.95 mm. There were 4 (12.1%) DCIS and 29 (87.8%) invasive cancers, including 1 (3.4%) TNBC. The median procedure time was 52 minutes, with all patients undergoing two freeze-thaw cycles. The median final iceball size was 50.6 mm. The median pain score one week post-ablation was 1 out of 10, with no significant complications reported. 82.6% of patients had follow-up imaging 6-week post-cryosurgery and biopsy. Additionally, 71.4% of the patients had completed 1-year postcryosurgery MRI/PET-CT. All displayed no radiological evidence of residual malignancy.<br></p><p>Conclusions: Cryoablation effectively ablated T1 BC, including TNBC. Further studies are needed to confirm its broader applicability. MRI scan is an essential tool to provide better patient selection</p>-
dc.languageeng-
dc.relation.ispartofGlobal Breast Cancer Conference 2025 (17/04/2025-19/04/2025, Seoul)-
dc.titleInitial experience on broadening the use of cryoablation on early breast cancer (Oral presentation)-
dc.typeConference_Paper-

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