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Clinical Trial
. 2022 Dec;23(12):1517-1524.
doi: 10.1016/S1470-2045(22)00613-1. Epub 2022 Oct 25.

Eliminating breast surgery for invasive breast cancer in exceptional responders to neoadjuvant systemic therapy: a multicentre, single-arm, phase 2 trial

Collaborators, Affiliations
Clinical Trial

Eliminating breast surgery for invasive breast cancer in exceptional responders to neoadjuvant systemic therapy: a multicentre, single-arm, phase 2 trial

Henry M Kuerer et al. Lancet Oncol. 2022 Dec.

Abstract

Background: Neoadjuvant systemic therapy (NST) for triple-negative breast cancer and HER2-positive breast cancer yields a pathological complete response in approximately 60% of patients. A pathological complete response to NST predicts an excellent prognosis and can be accurately determined by percutaneous image-guided vacuum-assisted core biopsy (VACB). We evaluated radiotherapy alone, without breast surgery, in patients with early-stage triple-negative breast cancer or HER2-positive breast cancer treated with NST who had an image-guided VACB-determined pathological complete response.

Methods: This multicentre, single-arm, phase 2 trial was done in seven centres in the USA. Women aged 40 years or older who were not pregnant with unicentric cT1-2N0-1M0 triple-negative breast cancer or HER2-positive breast cancer and a residual breast lesion less than 2 cm on imaging after clinically standard NST were eligible for inclusion. Patients had one biopsy (minimum of 12 cores) obtained by 9G image-guided VACB of the tumour bed. If no invasive or in-situ disease was identified, breast surgery was omitted, and patients underwent standard whole-breast radiotherapy (40 Gy in 15 fractions or 50 Gy in 25 fractions) plus a boost (14 Gy in seven fractions). The primary outcome was the biopsy-confirmed ipsilateral breast tumour recurrence rate determined using the Kaplan-Meier method assessed in the per-protocol population. Safety was assessed in all patients who received VACB. This study has completed accrual and is registered with ClinicalTrials.gov, NCT02945579.

Findings: Between March 6, 2017, and Nov 9, 2021, 58 patients consented to participate; however, four (7%) did not meet final inclusion criteria and four (7%) withdrew consent. 50 patients were enrolled and underwent VACB following NST. The median age of the enrolled patients was 62 years (IQR 55-77); 21 (42%) patients had triple-negative breast cancer and 29 (58%) had HER2-positive breast cancer. VACB identified a pathological complete response in 31 patients (62% [95% CI 47·2-75·4). At a median follow-up of 26·4 months (IQR 15·2-39·6), no ipsilateral breast tumour recurrences occurred in these 31 patients. No serious biopsy-related adverse events or treatment-related deaths occurred.

Interpretation: Eliminating breast surgery in highly selected patients with an image-guided VACB-determined pathological complete response following NST is feasible with promising early results; however, additional prospective clinical trials evaluating this approach are needed.

Funding: US National Cancer Institute (National Institutes of Health).

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Conflict of interest statement

Declaration of interests HMK reports consulting fees from Merck; honorarium from Physicians Education Resources; payment as an Editor from the New England Journal of Medicine Group; royalties from McGraw-Hill Professional and Elsevier Publishing; and leadership role in National Surgical Adjuvant Breast and Bowel Project, the Radiation Therapy Oncology Group, and the Gynecologic Oncology Group oncology Clinical Trials Cooperative Group, Breast Cancer Committee, local-regional member. BDS reports salary support from Varian Medical Systems and a royalty and equity interest in Oncora Medical. SK reports consulting fees from AstraZeneca, and royalties from Elsevier Publishing. WTY reports royalties from Elsevier Publishing. VV reports a grant from Zymeworks, consulting and honoraria from Genentech/Roche, Novartis, and AstraZeneca; and leadership roles in the NRG Breast Committee and Trio Health Scientific Steering. JCB reports research funding from MD Anderson Cancer Center and SymBioSis paid to their institution. All other authors declare no competing interests.

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