Axillary lymph node status remains a top prognostic indicator for patients with breast cancer. It has been well established that the extent of nodal involvement plays a key role in the risk for both local recurrence and overall survival, and nodal staging has a tremendous impact on systemic therapy and radiotherapy treatment recommendations.During the last 25 years, significant changes in our nodal assessment techniques have occurred, with a trend toward less invasive and less extensive dissections. After NSABP B-32, sentinel lymph node biopsy (SLNB) alone became the standard of care for nodal staging of clinically node-negative (cN0) patients.1 Then, ACOSOG Z0011 illustrated the safety of SLNB alone in conjunction with adjuvant whole-breast radiation for women with T1 or T2 tumors undergoing lumpectomy with two or fewer positive sentinel lymph nodes (SLN), thereby avoiding axillary lymph node dissection (ALND) for 84% of SLNB-positive patients.2 However, there continues to be a marked interest in identifying even less invasive, yet oncologically safe, strategies to establish nodal status.The use of axillary ultrasound (AUS) was initially described in 1989 3 and its use has expanded significantly during the last 25 years. The potential benefit of AUS is the ability to triage patients with nodal metastases for upfront ALND, thus avoiding the time and cost of a staged SLNB/ ALND. However, this strategy potentially results in unnecessary ALND for women who would otherwise meet the Z0011 criteria. The role of AUS staging is especially controversial in the setting of patients undergoing neoadjuvant chemotherapy (NAC).In this study by Barrio et al., 4 the ability of pre-NAC AUS to predict nodal metastases after NAC was investigated with 402 cN0 patients receiving NAC between 2008 and 2016. Clinical nodal staging was performed by physical examination and collected by chart review. Of the 162 AUS procedures performed, 131 (81%) showed abnormal lymph nodes. Pathologic staging of these lymph nodes was performed via SLNB before NAC, SLNB alone, SLNB then ALND, or ALND alone. The incidence of positive lymph nodes after NAC was higher, yet not significantly different statistically (p = 0.1), for patients with an abnormal pre-NAC AUS. However, if abnormal axillary lymph nodes were identified on magnetic resonance imaging (MRI) or positron emission tomography (PET) and computed tomography (CT) before NAC, the patients had a significantly greater chance of having histologically positive lymph nodes (pN1) after NAC (p \ 0.001 for both). Differences in tumor biology were found between the patients with pN1 after NAC and the pathologically node-negative (pN0) patients. Nodal disease was more likely to be identified after NAC in the patients with nonductal histology [odds ratio (OR) 2.93; p = 0.003) and in those with estrogen receptor (ER) positivity (OR 3.94; p \ 0.001).The lower rate of response to NAC among patients with invasive lobular cancer and ER ? disease has been illustrated in previous studies. 5,6 In the entire patient ...