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Omission of Breast Surgery in Predicted Pathologic Complete Response after Neoadjuvant Systemic Therapy: A Multicenter, Single-Arm, Non-inferiority Trialopen access

Authors
정지정천종호김수연고지원유재민YOO TAE KYUNG R신희철안성귀박세호임우성남상은박민호김구상강태우이지연윤현조김유석윤창익김홍규문형곤한원식조나리야김민균이한별
Issue Date
Feb-2024
Publisher
한국유방암학회
Keywords
Biopsy; Breast Neoplasms; Clinical Trial; Multicenter Study; Neoadjuvant Therapy
Citation
Journal of Breast Cancer, v.27, no.1, pp 61 - 71
Pages
11
Journal Title
Journal of Breast Cancer
Volume
27
Number
1
Start Page
61
End Page
71
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/72991
DOI
10.4048/jbc.2023.0265
ISSN
1738-6756
2092-9900
Abstract
Purpose Advances in chemotherapeutic and targeted agents have increased pathologic complete response (pCR) rates after neoadjuvant systemic therapy (NST). Vacuum-assisted biopsy (VAB) has been suggested to accurately evaluate pCR. This study aims to confirm the non-inferiority of the 5-year disease-free survival of patients who omitted breast surgery when predicted to have a pCR based on breast magnetic resonance imaging (MRI) and VAB after NST, compared with patients with a pCR who had undergone breast surgery in previous studies.Methods The Omission of breast surgery for PredicTed pCR patients wIth MRI and vacuum-assisted bIopsy in breaST cancer after neoadjuvant systemic therapy (OPTIMIST) trial is a prospective, multicenter, single-arm, non-inferiority study enrolling in 17 tertiary care hospitals in the Republic of Korea. Eligible patients must have a clip marker placed in the tumor and meet the MRI criteria suggesting complete clinical response (post-NST MRI size ≤ 1 cm and lesion-to-background signal enhancement ratio ≤ 1.6) after NST. Patients will undergo VAB, and breast surgery will be omitted for those with no residual tumor. Axillary surgery can also be omitted if the patient was clinically node-negative before and after NST and met the stringent criteria of MRI size ≤ 0.5 cm. Survival and efficacy outcomes are evaluated over five years.Discussion This study seeks to establish evidence for the safe omission of breast surgery in exceptional responders to NST while minimizing patient burden. The trial will address concerns about potential undertreatment due to false-negative results and recurrence as well as improved patient-reported quality of life issues from the omission of surgery. Successful completion of this trial may reshape clinical practice for certain breast cancer subtypes and lead to a safe and less invasive approach for selected patients.Trial Registration ClinicalTrials.gov Identifier: NCT05505357. Registered on August 17, 2022.Clinical Research Information Service Identifier: KCT0007638. Registered on July 25, 2022.
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